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          "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Clinical subgroups&#46;</p> <p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">CAM&#44; cancer-associated myositis&#59; DM&#44; idiopathic dermatomyositis&#59; IBM&#44; inclusion body myopathy&#59; IMNM&#44; immune-mediated necrotizing myositis&#59; JM&#44; juvenile myositis&#59; PM&#44; idiopathic polymyositis&#59; OS&#44; overlap syndrome&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Idiopathic inflammatory myopathies &#40;IIM&#41; comprise a heterogenic group of systemic diseases that are characterized by nonsuppurative inflammation of skeletal muscle and progressive muscle weakness&#44; occasionally accompanied by systemic manifestations&#46; It is considered a rare disease with a worldwide mean incidence between 19<span class="elsevierStyleHsp" style=""></span>cases&#47;million population per year&#46;<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">1</span></a> This varies depending on the geographic region&#44; the research methods utilized and the classification criteria applied&#46; Before the use of steroids and immunosuppressive therapy&#44; the rates of mortality were high&#46;<a class="elsevierStyleCrossRefs" href="#bib0165"><span class="elsevierStyleSup">2&#44;3</span></a> The generalized utilization of these treatments&#44; as well as early diagnosis&#44; resulted in a significant improvement in survival&#46;<a class="elsevierStyleCrossRefs" href="#bib0175"><span class="elsevierStyleSup">4&#8211;6</span></a> The clinical manifestations of IIM&#44; as well as its course and prognosis&#44; are extremely heterogeneous&#44; which together with its low prevalence and the lack of multicenter studies&#44; makes the study of the disease a difficult undertaking&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">To date&#44; multicenter studies of IIM in the rheumatology setting have not been performed either in the Community of Madrid or in the rest of Spain&#46; For this reason&#44; and with the support of the Society of Rheumatology of the Community of Madrid &#40;SORCOM&#41;&#44; we proposed the creation of a group for the Registry of Inflammatory Myopathies in the autonomous community of Madrid &#40;REMICAM&#41; for the cross-sectional registry of patients&#44; the period of inclusion of which has concluded&#46; The availability of a multicenter observational registry of patients with IIM could enable us to envision the reality of this disease in the Community of Madrid&#44; as well as to determine the rates of morbidity and mortality and compare subgroups of patients&#44; in a disease whose rarity limits the possibility of obtaining significant data&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Patients and Methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Study Objectives</span><p id="par0015" class="elsevierStylePara elsevierViewall">The main objectives of the REMICAM are to describe and characterize IIM patients&#44; who usually managed in the rheumatology departments of the Community of Madrid&#44; for the purpose of&#58;<ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">1&#46;</span><p id="par0020" class="elsevierStylePara elsevierViewall">Describing the sociodemographic and clinical characteristics</p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">2&#46;</span><p id="par0025" class="elsevierStylePara elsevierViewall">Studying the rate of comorbidity and the cumulative incidence&#44; and possible differences among distinct types of myopathies</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">3&#46;</span><p id="par0030" class="elsevierStylePara elsevierViewall">Calculating the mortality rate in the overall series and by clinical subgroups</p></li></ul></p><p id="par0035" class="elsevierStylePara elsevierViewall">As secondary objectives&#44; the registry proposes a multicenter collaborative study to subsequently examine specific aspects of autoimmune inflammatory myopathies&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Study Design</span><p id="par0040" class="elsevierStylePara elsevierViewall">Retrospective multicenter registry of patients with IIM from units or departments of rheumatology in the Community of Madrid&#44; using a hospital-based cross-sectional registry&#44; recording retrospective information on clinical data&#44; mortality and cause of death&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Patient Selection</span><p id="par0045" class="elsevierStylePara elsevierViewall">Through SORCOM&#44; the invitation to participate in the present study was sent to the different departments or units of rheumatology of public hospitals in the Community of Madrid&#44; as well as the rheumatology department of Hospital Madrid Norte in Sanchinarro&#44; a borough of Madrid&#46; We included unselected consecutive patients with a diagnosis of IIM &#40;dermatomyositis&#44; polymyositis&#44; inclusion body myositis and immune-mediated necrotizing myositis&#41;&#44; who had undergone follow-up in the above departments at some time during the period between January 1980 and December 2014&#44; without taking into account their age at onset of the process&#46; The patients ultimately selected met the criteria of Bohan and Peter<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">7&#44;8</span></a> and&#47;or Tanimoto&#39;s classification criteria&#44;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">9</span></a> and we excluded toxic and infectious myopathies and myopathies secondary to neuromuscular disease&#46; The patients were classified into 7 subgroups&#58; idiopathic polymyositis &#40;PM&#41;&#44; idiopathic dermatomyositis &#40;DM&#41;&#44; juvenile myositis &#40;JM&#41;&#44; IIM associated with another connective tissue disease &#40;overlap syndrome&#41;&#44; cancer-associated IIM&#44; inclusion body myositis<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">10</span></a> and immune-mediated necrotizing myositis&#46;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">11</span></a> Patients with overlap syndrome had to meet criteria for IIM and criteria for the following connective tissue diseases&#58; rheumatoid arthritis&#44;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">12</span></a> systemic sclerosis&#44;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">13</span></a> systemic lupus erythematosus&#44;<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">14</span></a> mixed connective tissue disease<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">15</span></a> or Sj&#246;gren&#39;s syndrome&#46;<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">16</span></a> We defined myositis as being cancer-associated in those cases in which cancer was diagnosed during the 3 years prior to or after the development of the myopathy&#44; similar to the approach used in previous studies&#46;<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">17</span></a> For the comparison of the different subgroups&#44; we only took into account the first 5 of those mentioned above&#44; given the low prevalence of inclusion body myositis and immune-mediated necrotizing myositis&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Variables</span><p id="par0050" class="elsevierStylePara elsevierViewall">In all&#44; 313 variables were included for each patient&#44; and were grouped in terms of their relation to sociodemographic characteristics&#44; classification&#44; mortality&#44; comorbidity&#44; clinical manifestations and analytical data&#44; as well as information regarding treatments&#46; All of these data were retrieved from the medical history of each patient&#46; Exhaustive monitoring for inconsistencies in the data was performed by an external company&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The sociodemographic data included information on sex&#44; race&#44; age at disease onset&#44; age at the last visit &#40;age of the patient at the time of the last visit available or age at the time of death&#41;&#44; disease duration &#40;time since the diagnosis and the last visit&#41;&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">General symptoms included weight loss &#62;10&#37; or fever not explained by causes other than the rheumatic disease&#46; Skin manifestations included Gottron&#39;s papules&#44; heliotrope rash&#44; Gottron&#39;s sign&#44; cutaneous vasculitis &#40;established by a compatible biopsy&#41;&#44; photosensitivity&#44; mechanic&#39;s hands&#44; nonspecific pruritus&#44; skin ulcers&#44; ischemic ulcers in fingertips&#44; periungual erythema and&#47;or macroscopic dilatation of nailfold capillaries&#44; hand edema and sclerodactyly&#46; The hematologic manifestations included anemia&#44; leukopenia or thrombocytopenia attributed to the disease&#44; after ruling out drug-related and infectious causes&#44; among others&#46; We took into account gastrointestinal manifestations such as&#58; dysphagia&#44; gastroesophageal reflux &#40;defined as suggestive clinical signs and upper gastrointestinal tract endoscopy and&#47;or pH-metry and&#47;or esophageal manometry showing evidence of gastrointestinal tract dysmotility&#44; after ruling out other causes&#41;&#44; upper&#47;lower gastrointestinal bleeding attributed to the disease &#40;defined as hematemesis&#44; melena or rectal bleeding&#44; after ruling out other causes&#41; and diarrhea or constipation attributed to the disease &#40;defined by compatible clinical signs&#44; after ruling out other causes&#41;&#46; As cardiovascular disease&#44; we included&#58; arterial or venous or pulmonary thromboembolic disease&#44; ischemic cardiomyopathy&#44; arrhythmias&#44; stroke and pulmonary hypertension&#46; Pulmonary hypertension was defined by echocardiogram &#40;estimated systolic pulmonary artery pressure &#91;sPAP&#93; &#8805;40<span class="elsevierStyleHsp" style=""></span>mmHg&#41; and&#47;or cardiac catheterization &#40;measured sPAP &#8805;25<span class="elsevierStyleHsp" style=""></span>mmHg&#41;&#46; Interstitial lung disease was diagnosed on the basis of compatible clinical signs &#40;recent onset dyspnea on exertion and&#47;or dry cough and&#47;or fever with no other origin&#41; and diagnostic chest radiographic images&#44; high-resolution computed tomography of the lungs and&#47;or compatible lung biopsy&#44; and&#47;or compatible respiratory function tests&#44; once other causes had been ruled out&#46; Interstitial lung disease was classified&#44; when possible&#44; depending on the result of the lung biopsy and&#47;or the radiologic image and&#44; in the case of disagreement&#44; a consensus was reached between the radiologist and the pathologist to define the following subtypes&#58; nonspecific interstitial pneumonia&#44; usual interstitial pneumonia&#44; bronchiolitis obliterans organizing pneumonia&#44; diffuse alveolar damage and cryptogenic pneumonia&#46; An infection was considered to be serious if it required hospital admission or led to death&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">The cause of death of patients in routine follow-up in their referral hospital was recorded in terms of the data on the medical history or the death certificate&#46; When a patient was lost to follow-up&#44; the attempt was made to make contact by telephone to determine the status of the patient&#44; as well as the cause and date of death&#46; The causes of death were classified according to 5 subgroups depending on the underlying cause&#58; infections&#44; cardiovascular event &#40;arrhythmia&#44; ischemic cardiomyopathy&#44; acute ischemic or hemorrhagic stroke&#44; pulmonary hypertension&#44; heart failure and pulmonary thromboembolism&#41;&#44; cancer&#44; interstitial lung disease and miscellaneous&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Statistical Analysis</span><p id="par0070" class="elsevierStylePara elsevierViewall">A significance level <span class="elsevierStyleItalic">&#945;</span> of &#46;05 was assumed for all of the statistical analyses&#46; Sociodemographic factors&#44; classification subgroups&#44; comorbidity and survival were assessed by basic descriptive statistical analysis&#46; For the description of the sample&#44; we used central tendency measures &#40;mean and median&#41; and dispersion &#40;standard deviation and interquartile range&#41;&#44; as well as frequency tables and percentage distribution for continuous and categorical variables&#44; respectively&#46; The comparison of the distinct types of myopathies was done using mean difference tests&#44; with analysis of variance&#44; comparison of proportions by means of chi-square test&#44; and Fisher&#39;s exact test in cases of cell sizes less than 5&#46; All of the analyses were performed with Stata 12&#46;</p></span></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Results</span><p id="par0075" class="elsevierStylePara elsevierViewall">The sample was comprised of 479 patients from rheumatology departments or units from 12 hospitals of the Community of Madrid &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46; Seventy patients &#40;14&#46;6&#37;&#41; had been lost to follow-up at the time of inclusion in the registry&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Classification and Diagnosis</span><p id="par0080" class="elsevierStylePara elsevierViewall">The most widespread myopathy subgroups were the primary forms &#40;PM and DM&#41;&#44; followed by overlap syndrome&#44; juvenile myositis and cancer-associated myositis&#46; Moreover&#44; there were 6 cases of inclusion body myositis and 6 patients with immune-mediated necrotizing myositis &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Of the 6 patients with immune-mediated necrotizing myositis&#44; only 1 had undergone treatment with statins and 3 had not&#46; It was not possible to obtain this information for the other 2 patients&#46; The connective tissue disease most frequently associated with IIM in overlap syndrome was mixed connective tissue disease&#44; followed by systemic sclerosis&#44; systemic lupus erythematosus&#44; Sj&#246;gren&#39;s syndrome and rheumatoid arthritis &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; In all&#44; 99&#46;6&#37; met the criteria of Bohan and Peter&#44; 97&#46;3&#37; Tanimoto&#39;s criteria&#44; and 96&#46;9&#37; both&#46; According to the classification criteria proposed by Bohan and Peter&#44; 99&#46;6&#37; of the patients would have a possible disease&#44; 94&#46;1&#37; a probable disease and 67&#46;4&#37; a definite disease&#46; All of the patients but 1 with a diagnosis of overlap syndrome had a muscle biopsy compatible with myositis or electromyographic study with a typical myopathic pattern&#46; That patient was diagnosed with systemic sclerosis and had muscle weakness and a baseline creatine kinase &#40;CK&#41; level of 748<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#44; but later improved with treatment&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Demographic Data and Clinical Manifestations</span><p id="par0085" class="elsevierStylePara elsevierViewall">Most of the patients in our series were women &#40;74&#46;1&#37;&#41; and Caucasian &#40;93&#46;5&#37;&#41;&#46; The remaining sociodemographic data are shown in <a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>&#46; With regard to clinical manifestations&#44; there was a marked prevalence of interstitial lung disease &#40;29&#46;9&#37;&#41;&#44; mainly usual interstitial pneumonia &#40;28&#46;2&#37;&#41; and nonspecific interstitial pneumonia &#40;23&#46;4&#37;&#41;&#44; followed by bronchiolitis obliterans organizing pneumonia &#40;4&#37;&#41;&#44; diffuse alveolar damage &#40;2&#46;4&#37;&#41; and cryptogenic pneumonia &#40;0&#46;8&#37;&#41;&#59; it was not possible to identify the subtype of the remainder of the patients&#46; The CK levels in 11&#46;6&#37; of the patients were higher than normal at the end of follow-up&#44; and the follow-up period was longer in patients with normal CK levels &#40;10&#46;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8&#46;5 years vs 5&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#46;2 years&#59; <span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>&#46;001&#41;&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><p id="par0090" class="elsevierStylePara elsevierViewall">Patients with DM experienced a greater number of general symptoms when compared with those with PM&#44; and mechanic&#39;s hands and typical skin manifestations were more frequent&#46; Juvenile myositis was characterized by more frequent typical skin manifestations than was observed in dermatomyositis&#44; but Raynaud&#39;s phenomenon&#44; extramuscular manifestations&#44; malignant neoplasms and serious infections were less common&#46; On the other hand&#44; overlap syndrome was more frequently accompanied by arthritis&#44; Raynaud&#39;s phenomenon&#44; hematologic manifestations&#44; interstitial lung disease&#44; and systemic&#44; neuropsychiatric and renal manifestations&#46; Paraneoplastic myositis had a shorter follow-up and the patients had lower CK levels at the end of follow-up when compared to the other subgroups&#46; The most common myositis specific antibodies were anti-Jo-1 &#40;77 cases&#41;&#44; followed by anti-RNP&#44; anti-Mi-2&#44; anti-PM-Scl and others less frequent &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; The remaining clinical manifestations are shown in <a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Comorbidity and Complications</span><p id="par0095" class="elsevierStylePara elsevierViewall">Overall&#44; 54&#46;6&#37; of the patients had some cardiovascular risk factor&#44; mostly dyslipidemia&#44; hypertension&#44; diabetes mellitus and active tobacco use&#44; and 22&#46;3&#37; of the cases were complicated by one or more cardiovascular events &#40;<a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>&#41;&#46;</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia><p id="par0100" class="elsevierStylePara elsevierViewall">In all&#44; 25&#37; of the patients had complications in the form of serious infections&#44; mainly lower respiratory tract infections &#40;63&#37;&#41;&#44; followed by urinary tract &#40;14&#37;&#41;&#44; gastrointestinal &#40;10&#37;&#41; and others that were less common&#46; In 30&#37; of the cases of serious infections&#44; the outcome was death&#46; Serious infections developed more frequently in patients with overlap syndrome and myopathy associated with a malignant neoplasm&#46; With regard to cancer-associated myositis&#44; the tumors most frequently involved were lung and skin cancer &#40;8 cases each&#41;&#44; lymphoma &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>7&#41; and breast cancer &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>6&#41;&#46; In 2 cases&#44; the origin of the cancer had not been determined&#46;</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Death and the Causes</span><p id="par0105" class="elsevierStylePara elsevierViewall">During the study period&#44; there were 114 deaths&#44; representing 28&#37; of the analysis sample&#46; The major causes were cancer&#44; infections and cardiovascular events &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#46; Patients with cancer-associated myositis had the worst prognosis&#44; followed by overlap syndrome&#44; whereas the patients with juvenile myositis had the best prognosis&#46;</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Treatment</span><p id="par0110" class="elsevierStylePara elsevierViewall">With regard to treatment&#44; a substantial number of the patients had received&#44; at some time&#44; glucocorticoids&#44; either intravenously &#40;15&#37;&#41; or orally &#40;99&#37;&#41;&#44; and half of them &#40;50&#46;3&#37;&#41; still required oral steroids when they visited their physician for the last time&#46; They were taking a dose of less than 30<span class="elsevierStyleHsp" style=""></span>mg&#47;day in 95&#37; of the cases at the end of follow-up&#46; In all&#44; 13&#46;2&#37; of the patients required more than 1 cycle of oral steroids over the course of the disease&#46; Immunosuppressive agents were utilized in 74&#46;1&#37; of those patients&#44; 30&#46;5&#37; of whom required the use of 2 or more drugs over the course of the disease &#40;with an average of 2&#46;4<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;9 immunosuppressive drugs in those cases&#41;&#46; The nonbiologic therapies most widely utilized&#44; in cumulative percentage&#44; were methotrexate &#40;48&#37;&#41;&#44; azathioprine &#40;40&#37;&#41;&#44; hydroxychloroquine &#40;16&#37;&#41; and cyclophosphamide &#40;9&#37;&#41;&#46; In all&#44; 9&#37; were treated with intravenous immunoglobulin and 12&#37; received biological therapy at some time &#40;the drug most frequently used was rituximab in 9&#37; of the cases&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a>&#41;&#46;</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia></span></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Discussion</span><p id="par0115" class="elsevierStylePara elsevierViewall">This is the first multicenter registry of inflammatory myopathies in the Community of Madrid&#44; and it provides the most extensive compilation of data up to now&#46; The registry was created for the purpose of retrospectively analyzing the clinical characteristics&#44; comorbidities and complications of autoimmune inflammatory myopathies in a multicenter study of 12 hospitals in the Community of Madrid&#46; We compared the clinical characteristics&#44; analytical findings and prognosis in the different subgroups of autoimmune inflammatory myopathies&#46;</p><p id="par0120" class="elsevierStylePara elsevierViewall">The criteria of Tanimoto&#44;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">9</span></a> published in 1995&#44; have a greater specificity than those of Bohan and Peter&#46;<a class="elsevierStyleCrossRefs" href="#bib0245"><span class="elsevierStyleSup">18&#44;19</span></a> The only 2 cases that did not meet the criteria of Bohan and Peter&#44; did conform to Tanimoto&#39;s criteria&#44; and corresponded to 2 patients with antisynthetase syndrome with elevated muscle enzymes&#44; arthritis&#44; general symptoms and interstitial lung disease in both cases&#44; and mechanic&#39;s hands in one&#46;</p><p id="par0125" class="elsevierStylePara elsevierViewall">Idiopathic inflammatory myopathies appear to be associated with a number of connective tissue diseases&#44; and are reported to have a highly variable incidence&#44; between 7&#37; and 60&#37;&#44; depending on the series&#46;<a class="elsevierStyleCrossRefs" href="#bib0185"><span class="elsevierStyleSup">6&#44;20&#8211;23</span></a> In the present study&#44; we employed widely accepted classification criteria&#44; to conclude that the patients actually did have a connective tissue disease associated with inflammatory myopathy&#46;<a class="elsevierStyleCrossRefs" href="#bib0215"><span class="elsevierStyleSup">12&#8211;16</span></a> In all&#44; 21&#37; of the cases were classified as overlap syndrome&#44; a prevalence that is very similar to that of a Hungarian series&#44;<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">20</span></a> although greater than that of another Spanish series from a single hospital&#46;<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">6</span></a> Some of the patients from that series were included in the present registry&#46; The differences observed in terms of the higher proportion of patients with overlap syndrome in the REMICAM with respect to the other Spanish series could be due to the development of new manifestations in those patients that enabled the diagnosis of other associated connective tissue diseases&#44; as was proposed by other authors&#44;<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">24</span></a> or to differences in the characteristics of the other patients included&#46;</p><p id="par0130" class="elsevierStylePara elsevierViewall">Only 11&#46;6&#37; of the patients had CK levels over the normal range at the end of follow-up&#44; a fact that may give an approximate idea of the patients in whom activity persisted&#46; Nevertheless&#44; the addition of other data&#44; such as those proposed by the Myositis Outcome Assessment Collaborative Study Group &#40;IMACS&#41; and the Paediatric Rheumatology International Trials Organisation &#40;PRINTO&#41; for the definition of disease activity&#44; such as measuring muscle strength&#44; global assessment of the disease by the patient&#47;parents and the physician using visual analogue scales&#44; questionnaires on physical function and other data&#44; could have given a more precise idea of disease activity&#46;<a class="elsevierStyleCrossRefs" href="#bib0280"><span class="elsevierStyleSup">25&#44;26</span></a> However&#44; retrospective study limits the collection of these data&#44; as well as data to evaluate disease relapse&#46;</p><p id="par0135" class="elsevierStylePara elsevierViewall">As was expected with respect to the clinical differences among the subgroups&#44; patients with overlap syndrome had a different disease&#44; with symptoms characteristic of other conditions&#44; mainly systemic sclerosis or systemic lupus erythematosus&#44; similar to the findings in other series&#46;<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">6</span></a> Concerning associated comorbidity&#44; it is noteworthy that early half of the patients had one or more cardiovascular risk factors&#44; dyslipidemia being the most prevalent&#44; followed by hypertension&#46;</p><p id="par0140" class="elsevierStylePara elsevierViewall">The incidence of cancer in myopathy varies widely from one report to another&#44;<a class="elsevierStyleCrossRefs" href="#bib0290"><span class="elsevierStyleSup">27&#44;28</span></a> depending mostly on the definition of the subgroup of cancer-associated myositis&#44; as well as the age and sex of the patients&#44; and the characteristics of the series&#46; The REMICAM cohort had a lower incidence than the majority of the series in the literature&#46; This is probably due to the definition of cancer-associated myositis&#44; as well as to the inclusion of patients with overlap syndrome and the lower percentage of cases of DM&#44; which has classically been related to a higher risk of cancer&#46;<a class="elsevierStyleCrossRefs" href="#bib0185"><span class="elsevierStyleSup">6&#44;17</span></a></p><p id="par0145" class="elsevierStylePara elsevierViewall">Overall mortality in REMICAM was 28&#46;5&#37;&#44; similar to that of another Spanish and Asian series&#44; but higher than that of other patient populations&#46;<a class="elsevierStyleCrossRefs" href="#bib0185"><span class="elsevierStyleSup">6&#44;29</span></a> The most frequent cause of death was cancer&#44; closely followed by infections and cardiovascular events&#44; as has been reported by others&#46;<a class="elsevierStyleCrossRefs" href="#bib0305"><span class="elsevierStyleSup">30&#44;31</span></a> In the majority of the series&#44; mortality depends on the inclusion criteria utilized&#44; on the associated diseases&#44; the duration of patient follow-up and&#44; decisively&#44; on the inclusion or exclusion of cancer-associated myositis&#44; which has a negative effect on the prognosis&#46; Thus&#44; the higher survival of in some series could be due to the exclusion of cancer-associated myositis&#44; to the higher proportion of cases of juvenile disease&#44; to the younger age of the patients and to the high rate of lost studies&#46;<a class="elsevierStyleCrossRefs" href="#bib0175"><span class="elsevierStyleSup">4&#44;5</span></a></p><p id="par0150" class="elsevierStylePara elsevierViewall">This report is susceptible to selection biases&#44; mainly related to the method of selecting the centers&#46; For example&#44; it could be that the patients in the hospitals interested in participating were in poorer health or were studied more extensively&#46; However&#44; this bias is limited by the fact that the present study was also open to specialty centers&#44; where there would likely be more benign cases&#44; as well as to the fact that IIM are long-standing diseases and are associated with a high mortality rate&#44; which makes it probable that the majority of the patient were referred from tertiary centers at some time during the course of the disease&#46;</p><p id="par0155" class="elsevierStylePara elsevierViewall">On the other hand&#44; the retrospective design of the study impedes controlling the quality of the data&#44; allows the introduction of measuring errors and accessibility to information on important confounders&#46; However&#44; the low proportion of the loss of patients and the exhaustive monitoring for inconsistencies on the part of the external company makes it little likely that this limitation had an influential effect on the quality of the results&#46;</p><p id="par0160" class="elsevierStylePara elsevierViewall">To date&#44; REMICAM is the largest registry of patients with myopathy in the Community of Madrid&#44; and in the rest of Spain&#44; in the rheumatology setting&#44; based on a detailed study of clinical characteristics&#44; morbidity&#44; mortality and clinical subgroups&#46; The performance of further substudies will enable us to expand our knowledge on the course of this disease&#46;</p></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Ethical Disclosures</span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Protection of human and animal subjects</span><p id="par0165" class="elsevierStylePara elsevierViewall">The authors declare that no experiments were performed on humans or animals for this study&#46;</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Confidentiality of data</span><p id="par0170" class="elsevierStylePara elsevierViewall">The authors declare that they have followed the protocols of their work center on the publication of patient data&#46;</p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Right to privacy and informed consent</span><p id="par0175" class="elsevierStylePara elsevierViewall">The authors have obtained the written informed consent of the patients or subjects mentioned in the article&#46; The corresponding author is in possession of this document&#46;</p></span></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Funding</span><p id="par0180" class="elsevierStylePara elsevierViewall">The work for the present study was partially financed by a grant from <span class="elsevierStyleGrantSponsor" id="gs1">SORCOM-MSD</span>&#46;</p></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0160">Conflicts of Interest</span><p id="par0185" class="elsevierStylePara elsevierViewall">The authors declare they have no conflicts of interest&#46;</p></span></span>"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Objective</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">To analyze clinical characteristics&#44; survival and causes of death of patients diagnosed with autoimmune inflammatory myositis in the REMICAM registry from the Society of Rheumatology in the Community of Madrid &#40;SORCOM&#41;&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Methods</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Multicenter cohort of patients diagnosed with autoimmune inflammatory myopathy with follow-up between January 1980 and December 2014&#46; A total of 313 variables concerning demographic&#44; clinical and morbidity data were collected&#44; and a comparison was performed between clinical subgroups&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">A total of 479 patients were recruited from 12 centers with 14&#37; of patients lost to follow-up&#46; Seventy-four percent of cases were women&#44; age at diagnosis of 44<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>23 years and a mean follow-up period of 10<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8 years&#46; The most frequent clinical subgroups were primary myositis &#40;PM 29&#37;&#44; DM 22&#37;&#41;&#44; followed by overlap myositis &#40;20&#46;5&#37;&#41;&#44; juvenile myositis &#40;18&#37;&#41;&#44; myositis associated with cancer &#40;8&#37;&#41;&#44; immune-mediated necrotizing myositis &#40;1&#37;&#41; and inclusion body myositis &#40;1&#37;&#41;&#46; During the follow-up period&#44; a total of 114 deaths &#40;28&#37;&#41; were registered&#44; the main causes being cancer &#40;24&#37;&#41;&#44; infections &#40;23&#37;&#41; and cardiovascular events &#40;21&#37;&#41;&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusions</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">A total of 479 patients were recruited in the REMICAM registry of inflammatory myopathies&#46; Including sociodemographic&#44; clinical and prognostic information&#44; it represents the largest Spanish multicenter registry to date in rheumatology&#44; and constitutes an important source for conducting further substudies&#46;</p></span>"
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        "resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Objetivos</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Describir las caracter&#237;sticas cl&#237;nicas&#44; mortalidad y causas de muerte de una serie de pacientes diagnosticados de miositis inflamatoria idiop&#225;tica del registro REMICAM de la Sociedad de Reumatolog&#237;a de la Comunidad de Madrid &#40;SORCOM&#41;&#46;</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">M&#233;todos</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Estudio descriptivo retrospectivo multic&#233;ntrico de una cohorte de pacientes con diagn&#243;stico de miositis inflamatoria idiop&#225;tica en seguimiento en servicios de reumatolog&#237;a de hospitales de la Comunidad de Madrid entre enero de 1980 y diciembre de 2014&#46; Se han recogido hasta un total de 313 variables acerca de aspectos demogr&#225;ficos&#44; cl&#237;nicos y de morbimortalidad&#44; y se ha realizado una comparaci&#243;n entre subgrupos cl&#237;nicos&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Se han reclutado 479 pacientes procedentes de 12 centros&#44; con un 14&#37; de p&#233;rdidas durante el periodo de seguimiento&#46; El 74&#37; de los casos eran mujeres&#44; una edad al diagn&#243;stico de 44<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>23 a&#241;os&#44; y una media de seguimiento de 10<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8 a&#241;os&#46; Los subgrupos cl&#237;nicos m&#225;s frecuentes fueron las formas primarias &#40;PM 29&#37;&#44; DM 22&#37;&#41;&#44; seguidas de s&#237;ndrome de solapamiento &#40;20&#44;5&#37;&#41;&#44; miopat&#237;as juveniles &#40;18&#37;&#41;&#44; miopat&#237;as asociadas a c&#225;ncer &#40;8&#37;&#41;&#44; miopat&#237;as necrosantes inmunomediadas &#40;1&#37;&#41; y miositis por cuerpos de inclusi&#243;n &#40;1&#37;&#41;&#46; Durante el periodo de seguimiento se produjeron un total de 114 fallecimientos &#40;28&#37;&#41;&#44; siendo las principales causas el c&#225;ncer &#40;24&#37;&#41;&#44; las infecciones &#40;23&#37;&#41; y los eventos cardiovasculares &#40;21&#37;&#41;&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclusiones</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">En el registro REMICAM de miopat&#237;as inflamatorias de la Comunidad de Madrid se han reclutado 479 casos de miositis inflamatoria idiop&#225;tica con datos sociodemogr&#225;ficos&#44; cl&#237;nicos y pron&#243;sticos&#44; suponiendo el mayor registro multic&#233;ntrico espa&#241;ol en el &#225;mbito de la Reumatolog&#237;a hasta la fecha&#44; y constituyendo una fuente importante para la realizaci&#243;n de posteriores subestudios&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0020">Please cite this article as&#58; Nu&#241;o L&#44; Joven B&#44; Carreira P&#44; Maldonado V&#44; Larena C&#44; Llorente I&#44; et al&#46; Registro de pacientes con miopat&#237;a inflamatoria de la Sociedad Madrile&#241;a de Reumatolog&#237;a&#58; an&#225;lisis descriptivo&#46; Reumatol Clin&#46; 2017&#59;13&#58;331&#8211;337&#46;</p>"
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          "en" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Cumulative and current treatment&#46;</p> <p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Anti-TNF&#945;&#44; anti-tumor necrosis factor &#945;&#59; AZA&#44; azathioprine&#59; CP&#44; cyclophosphamide&#59; CyA&#44; cyclosporine A&#59; HCQ&#44; hydroxychloroquine&#59; IVIG&#44; intravenous immunoglobulins&#59; LEF&#44; leflunomide&#59; MMF&#44; mycophenolate mofetil&#59; MTX&#44; methotrexate&#59; PRED&#44; prednisone&#59; RTX&#44; rituximab&#46;</p>"
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                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Hospital &#40;No&#46;<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>479&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">n &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">La Paz&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">57 &#40;11&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Ram&#243;n y Cajal&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">38 &#40;7&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">La Princesa&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">14 &#40;2&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Puerta de Hierro&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">14 &#40;2&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Fundaci&#243;n Alcorc&#243;n&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">5 &#40;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Sanchinarro&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">14 &#40;2&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Gregorio Mara&#241;&#243;n&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">169 &#40;35&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Infanta Sof&#237;a&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">6 &#40;1&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Pr&#237;ncipe de Asturias&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">11 &#40;2&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Infanta Leonor&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">4 &#40;0&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Doce de Octubre&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">134 &#40;28&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Ni&#241;o Jes&#250;s&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">13 &#40;2&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
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          "leyenda" => "<p id="spar0100" class="elsevierStyleSimplePara elsevierViewall">CAM&#44; cancer-associated myositis&#59; CK&#44; creatine kinase&#59; DM&#44; idiopathic dermatomyositis&#59; ILD&#44; interstitial lung disease&#59; JM&#44; juvenile myositis&#59; PM&#44; idiopathic polymyositis&#59; OS&#44; overlap syndrome&#46;</p><p id="spar0105" class="elsevierStyleSimplePara elsevierViewall">Ages&#44; time since diagnosis and CK levels are expressed as mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>standard deviation&#59; the remaining variables are expressed as number and percentage &#40;in parenthesis&#41;&#46;</p>"
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                0 => """
                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head  " align="" valign="top" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">PM<br>&#40;No&#46;<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>137&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">DM<br>&#40;No&#46;<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>107&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">JM<br>&#40;No&#46;<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>86&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">OS<br>&#40;No&#46;<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>98&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">CAM<br>&#40;No&#46;<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>39&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Total&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Age at diagnosis<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">54<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>17&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">50<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>16&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">45<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>17&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">62<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>11&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">43&#46;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>22&#46;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Age at end of follow-up<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">62<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>17&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">60<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>15&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">17<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>10&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">55<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>17&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">62<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>11&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">52&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>22&#46;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Time since diagnosis<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">11<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">13<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">9&#46;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8&#46;3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Female sex<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">96 &#40;70&#46;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">86 &#40;80&#46;4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">61 &#40;70&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">84 &#40;85&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">21 &#40;53&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">74&#46;1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Arthritis<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">47 &#40;34&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">50 &#40;48&#46;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">24 &#40;28&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">64 &#40;66&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">11 &#40;29&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">196 &#40;42&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Skin manifestations<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">29 &#40;21&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">107 &#40;100&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">79 &#40;91&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">63 &#40;64&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">30 &#40;76&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">308 &#40;66&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Typical signs of DM<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">0&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">107 &#40;100&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">73 &#40;84&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">22 &#40;22&#46;4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">26 &#40;66&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">225 &#40;48&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Hematologic manifestations<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">28 &#40;20&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">26 &#40;24&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">16 &#40;18&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">52 &#40;53&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">11 &#40;28&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">133 &#40;28&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">ILD<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">48 &#40;35&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">33 &#40;30&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2 &#40;2&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">47 &#40;48&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">8 &#40;21&#46;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">138 &#40;29&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Gastrointestinal manifestations<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">33 &#40;24&#46;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">37 &#40;34&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">21 &#40;24&#46;4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">44 &#40;44&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">18 &#40;46&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">153 &#40;32&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Dysphagia<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">25 &#40;18&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">28 &#40;26&#46;4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">19 &#40;22&#46;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">41 &#40;41&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">11 &#40;28&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">124 &#40;26&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">General manifestations<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">41 &#40;30&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">46 &#40;44&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">25 &#40;31&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">50 &#40;51&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">16 &#40;45&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">178 &#40;39&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Cardiac manifestations<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">34 &#40;24&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">19 &#40;17&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">6 &#40;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">26 &#40;26&#46;5&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">9 &#40;23&#46;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">94 &#40;20&#46;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Pulmonary hypertension<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">10 &#40;7&#46;4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">11 &#40;10&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1 &#40;1&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">15 &#40;15&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1 &#40;2&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">38 &#40;8&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Muscle involvement&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">137 &#40;100&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">107 &#40;100&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">85 &#40;98&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">98 &#40;100&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">39 &#40;100&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">466 &#40;99&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Muscle weakness&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">129 &#40;94&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">104 &#40;97&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">80 &#40;93&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">95 &#40;96&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">38 &#40;97&#46;4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">446 &#40;95&#46;5&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Baseline CK level &#40;IU&#47;L&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2911<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4556&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1955<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3557&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2264<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3512&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1324<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>2478&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1900<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3538&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2161<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3723&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Final CK level &#40;IU&#47;L&#41;<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">305<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>655&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">122<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>153&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">199<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>457&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">142<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>301&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">87<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>96&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">192<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>445&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Calcinosis<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">3 &#40;2&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">9 &#40;8&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">27 &#40;31&#46;4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">10 &#40;10&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">0&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">49 &#40;10&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Raynaud&#39;s<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">23 &#40;16&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">21 &#40;19&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">12 &#40;14&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">64 &#40;65&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">13 &#40;33&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">133 &#40;28&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Serious infection<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">36 &#40;26&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">22 &#40;21&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">3 &#40;3&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">38 &#40;41&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">12 &#40;34&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">111 &#40;24&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Cancer<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">16 &#40;11&#46;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">8 &#40;7&#46;5&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1 &#40;1&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">6 &#40;6&#46;1&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">39 &#40;100&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">70 &#40;15&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Death<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">&#42;&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">32 &#40;26&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">19 &#40;21&#46;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">4 &#40;6&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">30 &#40;37&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">28 &#40;71&#46;8&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">113 &#40;28&#46;5&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
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                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Comorbidity&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">n &#40;&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">26 &#40;5&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1 &#40;0&#46;2&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">70 &#40;14&#46;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Death&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">114 &#40;27&#46;9&#41;&nbsp;\t\t\t\t\t\t\n
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Journal Information
Vol. 13. Issue 6.
Pages 331-337 (November - December 2017)
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8681
Vol. 13. Issue 6.
Pages 331-337 (November - December 2017)
Original Article
Full text access
Multicenter Registry on Inflammatory Myositis From the Rheumatology Society in Madrid, Spain: Descriptive Analysis
Registro de pacientes con miopatía inflamatoria de la Sociedad Madrileña de Reumatología: análisis descriptivo
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Laura Nuñoa,
Corresponding author
lauranuno2@hotmail.com

Corresponding author.
, Beatriz Jovenb, Patricia Carreirab, Valentina Maldonadoc, Carmen Larenac, Irene Llorented, Eva Tomerod, María Carmen Barbadilloe, Paloma García-de la Peñaf, Lucía Ruizg, Juan Carlos López-Robledillog, Henry Morunoh, Ana Pérezh, Tatiana Cobo-Ibáñezi, Raquel Almodóvarj, Leticia Lojok, Indalecio Monteagudol, María Jesús García-De Yébenesm, Francisco Javier López-Longol
a Servicio de Reumatología, Hospital La Paz, Madrid, Spain
b Servicio de Reumatología, Hospital Doce de Octubre, Madrid, Spain
c Servicio de Reumatología, Hospital Ramón y Cajal, Madrid, Spain
d Servicio de Reumatología, Hospital La Princesa, Madrid, Spain
e Servicio de Reumatología, Hospital Puerta de Hierro, Madrid, Spain
f Servicio de Reumatología, Hospital Madrid Norte Sanchinarro, Madrid, Spain
g Servicio de Reumatología, Hospital Infantil Niño Jesús, Madrid, Spain
h Servicio de Reumatología, Hospital Príncipe de Asturias, Madrid, Spain
i Servicio de Reumatología, Hospital Infanta Sofía, Madrid, Spain
j Servicio de Reumatología, Hospital Fundación Alcorcón, Madrid, Spain
k Servicio de Reumatología, Hospital Infanta Leonor, Madrid, Spain
l Servicio de Reumatología, Hospital Gregorio Marañón, Madrid, Spain
m Instituto de Salud Musculoesquelética, Madrid, Spain
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Table 1. Distribution of Patients by Hospital.
Table 2. Differential Clinical Characteristics According to Clinical Subgroup, n (%).
Table 3. Comorbidity and Complications.
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Abstract
Objective

To analyze clinical characteristics, survival and causes of death of patients diagnosed with autoimmune inflammatory myositis in the REMICAM registry from the Society of Rheumatology in the Community of Madrid (SORCOM).

Methods

Multicenter cohort of patients diagnosed with autoimmune inflammatory myopathy with follow-up between January 1980 and December 2014. A total of 313 variables concerning demographic, clinical and morbidity data were collected, and a comparison was performed between clinical subgroups.

Results

A total of 479 patients were recruited from 12 centers with 14% of patients lost to follow-up. Seventy-four percent of cases were women, age at diagnosis of 44±23 years and a mean follow-up period of 10±8 years. The most frequent clinical subgroups were primary myositis (PM 29%, DM 22%), followed by overlap myositis (20.5%), juvenile myositis (18%), myositis associated with cancer (8%), immune-mediated necrotizing myositis (1%) and inclusion body myositis (1%). During the follow-up period, a total of 114 deaths (28%) were registered, the main causes being cancer (24%), infections (23%) and cardiovascular events (21%).

Conclusions

A total of 479 patients were recruited in the REMICAM registry of inflammatory myopathies. Including sociodemographic, clinical and prognostic information, it represents the largest Spanish multicenter registry to date in rheumatology, and constitutes an important source for conducting further substudies.

Keywords:
Idiopathic inflammatory myopathies
Registry
Descriptive study
Resumen
Objetivos

Describir las características clínicas, mortalidad y causas de muerte de una serie de pacientes diagnosticados de miositis inflamatoria idiopática del registro REMICAM de la Sociedad de Reumatología de la Comunidad de Madrid (SORCOM).

Métodos

Estudio descriptivo retrospectivo multicéntrico de una cohorte de pacientes con diagnóstico de miositis inflamatoria idiopática en seguimiento en servicios de reumatología de hospitales de la Comunidad de Madrid entre enero de 1980 y diciembre de 2014. Se han recogido hasta un total de 313 variables acerca de aspectos demográficos, clínicos y de morbimortalidad, y se ha realizado una comparación entre subgrupos clínicos.

Resultados

Se han reclutado 479 pacientes procedentes de 12 centros, con un 14% de pérdidas durante el periodo de seguimiento. El 74% de los casos eran mujeres, una edad al diagnóstico de 44±23 años, y una media de seguimiento de 10±8 años. Los subgrupos clínicos más frecuentes fueron las formas primarias (PM 29%, DM 22%), seguidas de síndrome de solapamiento (20,5%), miopatías juveniles (18%), miopatías asociadas a cáncer (8%), miopatías necrosantes inmunomediadas (1%) y miositis por cuerpos de inclusión (1%). Durante el periodo de seguimiento se produjeron un total de 114 fallecimientos (28%), siendo las principales causas el cáncer (24%), las infecciones (23%) y los eventos cardiovasculares (21%).

Conclusiones

En el registro REMICAM de miopatías inflamatorias de la Comunidad de Madrid se han reclutado 479 casos de miositis inflamatoria idiopática con datos sociodemográficos, clínicos y pronósticos, suponiendo el mayor registro multicéntrico español en el ámbito de la Reumatología hasta la fecha, y constituyendo una fuente importante para la realización de posteriores subestudios.

Palabras clave:
Miopatía inflamatoria idiopática
Registro
Estudio descriptivo
Full Text
Introduction

Idiopathic inflammatory myopathies (IIM) comprise a heterogenic group of systemic diseases that are characterized by nonsuppurative inflammation of skeletal muscle and progressive muscle weakness, occasionally accompanied by systemic manifestations. It is considered a rare disease with a worldwide mean incidence between 19cases/million population per year.1 This varies depending on the geographic region, the research methods utilized and the classification criteria applied. Before the use of steroids and immunosuppressive therapy, the rates of mortality were high.2,3 The generalized utilization of these treatments, as well as early diagnosis, resulted in a significant improvement in survival.4–6 The clinical manifestations of IIM, as well as its course and prognosis, are extremely heterogeneous, which together with its low prevalence and the lack of multicenter studies, makes the study of the disease a difficult undertaking.

To date, multicenter studies of IIM in the rheumatology setting have not been performed either in the Community of Madrid or in the rest of Spain. For this reason, and with the support of the Society of Rheumatology of the Community of Madrid (SORCOM), we proposed the creation of a group for the Registry of Inflammatory Myopathies in the autonomous community of Madrid (REMICAM) for the cross-sectional registry of patients, the period of inclusion of which has concluded. The availability of a multicenter observational registry of patients with IIM could enable us to envision the reality of this disease in the Community of Madrid, as well as to determine the rates of morbidity and mortality and compare subgroups of patients, in a disease whose rarity limits the possibility of obtaining significant data.

Patients and MethodsStudy Objectives

The main objectives of the REMICAM are to describe and characterize IIM patients, who usually managed in the rheumatology departments of the Community of Madrid, for the purpose of:

  • 1.

    Describing the sociodemographic and clinical characteristics

  • 2.

    Studying the rate of comorbidity and the cumulative incidence, and possible differences among distinct types of myopathies

  • 3.

    Calculating the mortality rate in the overall series and by clinical subgroups

As secondary objectives, the registry proposes a multicenter collaborative study to subsequently examine specific aspects of autoimmune inflammatory myopathies.

Study Design

Retrospective multicenter registry of patients with IIM from units or departments of rheumatology in the Community of Madrid, using a hospital-based cross-sectional registry, recording retrospective information on clinical data, mortality and cause of death.

Patient Selection

Through SORCOM, the invitation to participate in the present study was sent to the different departments or units of rheumatology of public hospitals in the Community of Madrid, as well as the rheumatology department of Hospital Madrid Norte in Sanchinarro, a borough of Madrid. We included unselected consecutive patients with a diagnosis of IIM (dermatomyositis, polymyositis, inclusion body myositis and immune-mediated necrotizing myositis), who had undergone follow-up in the above departments at some time during the period between January 1980 and December 2014, without taking into account their age at onset of the process. The patients ultimately selected met the criteria of Bohan and Peter7,8 and/or Tanimoto's classification criteria,9 and we excluded toxic and infectious myopathies and myopathies secondary to neuromuscular disease. The patients were classified into 7 subgroups: idiopathic polymyositis (PM), idiopathic dermatomyositis (DM), juvenile myositis (JM), IIM associated with another connective tissue disease (overlap syndrome), cancer-associated IIM, inclusion body myositis10 and immune-mediated necrotizing myositis.11 Patients with overlap syndrome had to meet criteria for IIM and criteria for the following connective tissue diseases: rheumatoid arthritis,12 systemic sclerosis,13 systemic lupus erythematosus,14 mixed connective tissue disease15 or Sjögren's syndrome.16 We defined myositis as being cancer-associated in those cases in which cancer was diagnosed during the 3 years prior to or after the development of the myopathy, similar to the approach used in previous studies.17 For the comparison of the different subgroups, we only took into account the first 5 of those mentioned above, given the low prevalence of inclusion body myositis and immune-mediated necrotizing myositis.

Variables

In all, 313 variables were included for each patient, and were grouped in terms of their relation to sociodemographic characteristics, classification, mortality, comorbidity, clinical manifestations and analytical data, as well as information regarding treatments. All of these data were retrieved from the medical history of each patient. Exhaustive monitoring for inconsistencies in the data was performed by an external company.

The sociodemographic data included information on sex, race, age at disease onset, age at the last visit (age of the patient at the time of the last visit available or age at the time of death), disease duration (time since the diagnosis and the last visit).

General symptoms included weight loss >10% or fever not explained by causes other than the rheumatic disease. Skin manifestations included Gottron's papules, heliotrope rash, Gottron's sign, cutaneous vasculitis (established by a compatible biopsy), photosensitivity, mechanic's hands, nonspecific pruritus, skin ulcers, ischemic ulcers in fingertips, periungual erythema and/or macroscopic dilatation of nailfold capillaries, hand edema and sclerodactyly. The hematologic manifestations included anemia, leukopenia or thrombocytopenia attributed to the disease, after ruling out drug-related and infectious causes, among others. We took into account gastrointestinal manifestations such as: dysphagia, gastroesophageal reflux (defined as suggestive clinical signs and upper gastrointestinal tract endoscopy and/or pH-metry and/or esophageal manometry showing evidence of gastrointestinal tract dysmotility, after ruling out other causes), upper/lower gastrointestinal bleeding attributed to the disease (defined as hematemesis, melena or rectal bleeding, after ruling out other causes) and diarrhea or constipation attributed to the disease (defined by compatible clinical signs, after ruling out other causes). As cardiovascular disease, we included: arterial or venous or pulmonary thromboembolic disease, ischemic cardiomyopathy, arrhythmias, stroke and pulmonary hypertension. Pulmonary hypertension was defined by echocardiogram (estimated systolic pulmonary artery pressure [sPAP] ≥40mmHg) and/or cardiac catheterization (measured sPAP ≥25mmHg). Interstitial lung disease was diagnosed on the basis of compatible clinical signs (recent onset dyspnea on exertion and/or dry cough and/or fever with no other origin) and diagnostic chest radiographic images, high-resolution computed tomography of the lungs and/or compatible lung biopsy, and/or compatible respiratory function tests, once other causes had been ruled out. Interstitial lung disease was classified, when possible, depending on the result of the lung biopsy and/or the radiologic image and, in the case of disagreement, a consensus was reached between the radiologist and the pathologist to define the following subtypes: nonspecific interstitial pneumonia, usual interstitial pneumonia, bronchiolitis obliterans organizing pneumonia, diffuse alveolar damage and cryptogenic pneumonia. An infection was considered to be serious if it required hospital admission or led to death.

The cause of death of patients in routine follow-up in their referral hospital was recorded in terms of the data on the medical history or the death certificate. When a patient was lost to follow-up, the attempt was made to make contact by telephone to determine the status of the patient, as well as the cause and date of death. The causes of death were classified according to 5 subgroups depending on the underlying cause: infections, cardiovascular event (arrhythmia, ischemic cardiomyopathy, acute ischemic or hemorrhagic stroke, pulmonary hypertension, heart failure and pulmonary thromboembolism), cancer, interstitial lung disease and miscellaneous.

Statistical Analysis

A significance level α of .05 was assumed for all of the statistical analyses. Sociodemographic factors, classification subgroups, comorbidity and survival were assessed by basic descriptive statistical analysis. For the description of the sample, we used central tendency measures (mean and median) and dispersion (standard deviation and interquartile range), as well as frequency tables and percentage distribution for continuous and categorical variables, respectively. The comparison of the distinct types of myopathies was done using mean difference tests, with analysis of variance, comparison of proportions by means of chi-square test, and Fisher's exact test in cases of cell sizes less than 5. All of the analyses were performed with Stata 12.

Results

The sample was comprised of 479 patients from rheumatology departments or units from 12 hospitals of the Community of Madrid (Table 1). Seventy patients (14.6%) had been lost to follow-up at the time of inclusion in the registry.

Table 1.

Distribution of Patients by Hospital.

Hospital (No.=479)  n (%) 
La Paz  57 (11.9) 
Ramón y Cajal  38 (7.9) 
La Princesa  14 (2.9) 
Puerta de Hierro  14 (2.9) 
Fundación Alcorcón  5 (1) 
Sanchinarro  14 (2.9) 
Gregorio Marañón  169 (35.3) 
Infanta Sofía  6 (1.3) 
Príncipe de Asturias  11 (2.3) 
Infanta Leonor  4 (0.8) 
Doce de Octubre  134 (28) 
Niño Jesús  13 (2.7) 
Classification and Diagnosis

The most widespread myopathy subgroups were the primary forms (PM and DM), followed by overlap syndrome, juvenile myositis and cancer-associated myositis. Moreover, there were 6 cases of inclusion body myositis and 6 patients with immune-mediated necrotizing myositis (Fig. 1). Of the 6 patients with immune-mediated necrotizing myositis, only 1 had undergone treatment with statins and 3 had not. It was not possible to obtain this information for the other 2 patients. The connective tissue disease most frequently associated with IIM in overlap syndrome was mixed connective tissue disease, followed by systemic sclerosis, systemic lupus erythematosus, Sjögren's syndrome and rheumatoid arthritis (Fig. 2). In all, 99.6% met the criteria of Bohan and Peter, 97.3% Tanimoto's criteria, and 96.9% both. According to the classification criteria proposed by Bohan and Peter, 99.6% of the patients would have a possible disease, 94.1% a probable disease and 67.4% a definite disease. All of the patients but 1 with a diagnosis of overlap syndrome had a muscle biopsy compatible with myositis or electromyographic study with a typical myopathic pattern. That patient was diagnosed with systemic sclerosis and had muscle weakness and a baseline creatine kinase (CK) level of 748IU/L, but later improved with treatment.

Fig. 1.

Clinical subgroups.

CAM, cancer-associated myositis; DM, idiopathic dermatomyositis; IBM, inclusion body myopathy; IMNM, immune-mediated necrotizing myositis; JM, juvenile myositis; PM, idiopathic polymyositis; OS, overlap syndrome.

(0.08MB).
Fig. 2.

Connective tissue diseases associated with overlap syndrome.

MCTD, mixed connective tissue disease; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus; SS, Sjögren's syndrome; SSc, systemic sclerosis.

(0.05MB).
Demographic Data and Clinical Manifestations

Most of the patients in our series were women (74.1%) and Caucasian (93.5%). The remaining sociodemographic data are shown in Table 2. With regard to clinical manifestations, there was a marked prevalence of interstitial lung disease (29.9%), mainly usual interstitial pneumonia (28.2%) and nonspecific interstitial pneumonia (23.4%), followed by bronchiolitis obliterans organizing pneumonia (4%), diffuse alveolar damage (2.4%) and cryptogenic pneumonia (0.8%); it was not possible to identify the subtype of the remainder of the patients. The CK levels in 11.6% of the patients were higher than normal at the end of follow-up, and the follow-up period was longer in patients with normal CK levels (10.3±8.5 years vs 5.9±5.2 years; P<.001).

Table 2.

Differential Clinical Characteristics According to Clinical Subgroup, n (%).

  PM
(No.=137) 
DM
(No.=107) 
JM
(No.=86) 
OS
(No.=98) 
CAM
(No.=39) 
Total 
Age at diagnosis***  54±17  50±16  8±45±17  62±11  43.7±22.6 
Age at end of follow-up***  62±17  60±15  17±10  55±17  62±11  52.5±22.6 
Time since diagnosis***  8±11±8±13±5±9.7±8.3 
Female sex**  96 (70.1)  86 (80.4)  61 (70.9)  84 (85.7)  21 (53.8)  74.1 
Arthritis***  47 (34.6)  50 (48.1)  24 (28.2)  64 (66)  11 (29.7)  196 (42.7) 
Skin manifestations***  29 (21.2)  107 (100)  79 (91.9)  63 (64.3)  30 (76.9)  308 (66) 
Typical signs of DM***  107 (100)  73 (84.9)  22 (22.4)  26 (66.7)  225 (48.8) 
Hematologic manifestations***  28 (20.6)  26 (24.3)  16 (18.6)  52 (53.6)  11 (28.9)  133 (28.7) 
ILD***  48 (35)  33 (30.8)  2 (2.3)  47 (48)  8 (21.1)  138 (29.6) 
Gastrointestinal manifestations**  33 (24.1)  37 (34.6)  21 (24.4)  44 (44.9)  18 (46.2)  153 (32.8) 
Dysphagia**  25 (18.2)  28 (26.4)  19 (22.1)  41 (41.8)  11 (28.2)  124 (26.6) 
General manifestations*  41 (30.6)  46 (44.7)  25 (31.6)  50 (51)  16 (45.7)  178 (39.6) 
Cardiac manifestations**  34 (24.8)  19 (17.8)  6 (7)  26 (26.5)  9 (23.1)  94 (20.1) 
Pulmonary hypertension**  10 (7.4)  11 (10.3)  1 (1.2)  15 (15.3)  1 (2.6)  38 (8.2) 
Muscle involvement  137 (100)  107 (100)  85 (98.8)  98 (100)  39 (100)  466 (99.8) 
Muscle weakness  129 (94.2)  104 (97.2)  80 (93)  95 (96.9)  38 (97.4)  446 (95.5) 
Baseline CK level (IU/L)  2911±4556  1955±3557  2264±3512  1324±2478  1900±3538  2161±3723 
Final CK level (IU/L)*  305±655  122±153  199±457  142±301  87±96  192±445 
Calcinosis***  3 (2.2)  9 (8.6)  27 (31.4)  10 (10.2)  49 (10.6) 
Raynaud's***  23 (16.9)  21 (19.8)  12 (14)  64 (65.3)  13 (33.3)  133 (28.6) 
Serious infection***  36 (26.7)  22 (21)  3 (3.8)  38 (41.3)  12 (34.3)  111 (24.9) 
Cancer***  16 (11.7)  8 (7.5)  1 (1.2)  6 (6.1)  39 (100)  70 (15) 
Death***  32 (26)  19 (21.3)  4 (6.2)  30 (37)  28 (71.8)  113 (28.5) 

CAM, cancer-associated myositis; CK, creatine kinase; DM, idiopathic dermatomyositis; ILD, interstitial lung disease; JM, juvenile myositis; PM, idiopathic polymyositis; OS, overlap syndrome.

Ages, time since diagnosis and CK levels are expressed as mean±standard deviation; the remaining variables are expressed as number and percentage (in parenthesis).

*

P<.05.

**

P<.01.

***

P<.001.

Patients with DM experienced a greater number of general symptoms when compared with those with PM, and mechanic's hands and typical skin manifestations were more frequent. Juvenile myositis was characterized by more frequent typical skin manifestations than was observed in dermatomyositis, but Raynaud's phenomenon, extramuscular manifestations, malignant neoplasms and serious infections were less common. On the other hand, overlap syndrome was more frequently accompanied by arthritis, Raynaud's phenomenon, hematologic manifestations, interstitial lung disease, and systemic, neuropsychiatric and renal manifestations. Paraneoplastic myositis had a shorter follow-up and the patients had lower CK levels at the end of follow-up when compared to the other subgroups. The most common myositis specific antibodies were anti-Jo-1 (77 cases), followed by anti-RNP, anti-Mi-2, anti-PM-Scl and others less frequent (Fig. 3). The remaining clinical manifestations are shown in Table 2.

Fig. 3.

Myositis specific antibodies.

(0.05MB).
Comorbidity and Complications

Overall, 54.6% of the patients had some cardiovascular risk factor, mostly dyslipidemia, hypertension, diabetes mellitus and active tobacco use, and 22.3% of the cases were complicated by one or more cardiovascular events (Table 3).

Table 3.

Comorbidity and Complications.

Comorbidity  n (%) 
Cardiovascular disease  104 (22.3) 
Peripheral vascular disease  26 (5.6) 
Ischemic cardiomyopathy  28 (6) 
Stroke  23 (4.9) 
Pulmonary hypertension  38 (7.9) 
Heart failure  45 (9.6) 
Hypertension  146 (31.1) 
Diabetes mellitus  58 (12.4) 
Dyslipidemia  149 (31.8) 
Active tobacco use  64 (19.6) 
Cardiovascular risk factors (hypertension, diabetes, dyslipidemia, tobacco use)  261 (54.6) 
Number of cardiovascular risk factors
One  141 (29.9) 
Two  85 (18) 
Three  34 (7.2) 
Four  1 (0.2) 
Pulmonary disease  40 (8.5) 
Pleuritis  13 (2.7) 
COPD  27 (5.8) 
Complications
Serious infections  113 (24.7) 
Cancer  70 (14.6) 
Death  114 (27.9) 

COPD, chronic obstructive pulmonary disease.

In all, 25% of the patients had complications in the form of serious infections, mainly lower respiratory tract infections (63%), followed by urinary tract (14%), gastrointestinal (10%) and others that were less common. In 30% of the cases of serious infections, the outcome was death. Serious infections developed more frequently in patients with overlap syndrome and myopathy associated with a malignant neoplasm. With regard to cancer-associated myositis, the tumors most frequently involved were lung and skin cancer (8 cases each), lymphoma (n=7) and breast cancer (n=6). In 2 cases, the origin of the cancer had not been determined.

Death and the Causes

During the study period, there were 114 deaths, representing 28% of the analysis sample. The major causes were cancer, infections and cardiovascular events (Fig. 4). Patients with cancer-associated myositis had the worst prognosis, followed by overlap syndrome, whereas the patients with juvenile myositis had the best prognosis.

Fig. 4.

Causes of death in the overall series.

ILD, interstitial lung disease.

(0.08MB).
Treatment

With regard to treatment, a substantial number of the patients had received, at some time, glucocorticoids, either intravenously (15%) or orally (99%), and half of them (50.3%) still required oral steroids when they visited their physician for the last time. They were taking a dose of less than 30mg/day in 95% of the cases at the end of follow-up. In all, 13.2% of the patients required more than 1 cycle of oral steroids over the course of the disease. Immunosuppressive agents were utilized in 74.1% of those patients, 30.5% of whom required the use of 2 or more drugs over the course of the disease (with an average of 2.4±0.9 immunosuppressive drugs in those cases). The nonbiologic therapies most widely utilized, in cumulative percentage, were methotrexate (48%), azathioprine (40%), hydroxychloroquine (16%) and cyclophosphamide (9%). In all, 9% were treated with intravenous immunoglobulin and 12% received biological therapy at some time (the drug most frequently used was rituximab in 9% of the cases) (Fig. 5).

Fig. 5.

Cumulative and current treatment.

Anti-TNFα, anti-tumor necrosis factor α; AZA, azathioprine; CP, cyclophosphamide; CyA, cyclosporine A; HCQ, hydroxychloroquine; IVIG, intravenous immunoglobulins; LEF, leflunomide; MMF, mycophenolate mofetil; MTX, methotrexate; PRED, prednisone; RTX, rituximab.

(0.16MB).
Discussion

This is the first multicenter registry of inflammatory myopathies in the Community of Madrid, and it provides the most extensive compilation of data up to now. The registry was created for the purpose of retrospectively analyzing the clinical characteristics, comorbidities and complications of autoimmune inflammatory myopathies in a multicenter study of 12 hospitals in the Community of Madrid. We compared the clinical characteristics, analytical findings and prognosis in the different subgroups of autoimmune inflammatory myopathies.

The criteria of Tanimoto,9 published in 1995, have a greater specificity than those of Bohan and Peter.18,19 The only 2 cases that did not meet the criteria of Bohan and Peter, did conform to Tanimoto's criteria, and corresponded to 2 patients with antisynthetase syndrome with elevated muscle enzymes, arthritis, general symptoms and interstitial lung disease in both cases, and mechanic's hands in one.

Idiopathic inflammatory myopathies appear to be associated with a number of connective tissue diseases, and are reported to have a highly variable incidence, between 7% and 60%, depending on the series.6,20–23 In the present study, we employed widely accepted classification criteria, to conclude that the patients actually did have a connective tissue disease associated with inflammatory myopathy.12–16 In all, 21% of the cases were classified as overlap syndrome, a prevalence that is very similar to that of a Hungarian series,20 although greater than that of another Spanish series from a single hospital.6 Some of the patients from that series were included in the present registry. The differences observed in terms of the higher proportion of patients with overlap syndrome in the REMICAM with respect to the other Spanish series could be due to the development of new manifestations in those patients that enabled the diagnosis of other associated connective tissue diseases, as was proposed by other authors,24 or to differences in the characteristics of the other patients included.

Only 11.6% of the patients had CK levels over the normal range at the end of follow-up, a fact that may give an approximate idea of the patients in whom activity persisted. Nevertheless, the addition of other data, such as those proposed by the Myositis Outcome Assessment Collaborative Study Group (IMACS) and the Paediatric Rheumatology International Trials Organisation (PRINTO) for the definition of disease activity, such as measuring muscle strength, global assessment of the disease by the patient/parents and the physician using visual analogue scales, questionnaires on physical function and other data, could have given a more precise idea of disease activity.25,26 However, retrospective study limits the collection of these data, as well as data to evaluate disease relapse.

As was expected with respect to the clinical differences among the subgroups, patients with overlap syndrome had a different disease, with symptoms characteristic of other conditions, mainly systemic sclerosis or systemic lupus erythematosus, similar to the findings in other series.6 Concerning associated comorbidity, it is noteworthy that early half of the patients had one or more cardiovascular risk factors, dyslipidemia being the most prevalent, followed by hypertension.

The incidence of cancer in myopathy varies widely from one report to another,27,28 depending mostly on the definition of the subgroup of cancer-associated myositis, as well as the age and sex of the patients, and the characteristics of the series. The REMICAM cohort had a lower incidence than the majority of the series in the literature. This is probably due to the definition of cancer-associated myositis, as well as to the inclusion of patients with overlap syndrome and the lower percentage of cases of DM, which has classically been related to a higher risk of cancer.6,17

Overall mortality in REMICAM was 28.5%, similar to that of another Spanish and Asian series, but higher than that of other patient populations.6,29 The most frequent cause of death was cancer, closely followed by infections and cardiovascular events, as has been reported by others.30,31 In the majority of the series, mortality depends on the inclusion criteria utilized, on the associated diseases, the duration of patient follow-up and, decisively, on the inclusion or exclusion of cancer-associated myositis, which has a negative effect on the prognosis. Thus, the higher survival of in some series could be due to the exclusion of cancer-associated myositis, to the higher proportion of cases of juvenile disease, to the younger age of the patients and to the high rate of lost studies.4,5

This report is susceptible to selection biases, mainly related to the method of selecting the centers. For example, it could be that the patients in the hospitals interested in participating were in poorer health or were studied more extensively. However, this bias is limited by the fact that the present study was also open to specialty centers, where there would likely be more benign cases, as well as to the fact that IIM are long-standing diseases and are associated with a high mortality rate, which makes it probable that the majority of the patient were referred from tertiary centers at some time during the course of the disease.

On the other hand, the retrospective design of the study impedes controlling the quality of the data, allows the introduction of measuring errors and accessibility to information on important confounders. However, the low proportion of the loss of patients and the exhaustive monitoring for inconsistencies on the part of the external company makes it little likely that this limitation had an influential effect on the quality of the results.

To date, REMICAM is the largest registry of patients with myopathy in the Community of Madrid, and in the rest of Spain, in the rheumatology setting, based on a detailed study of clinical characteristics, morbidity, mortality and clinical subgroups. The performance of further substudies will enable us to expand our knowledge on the course of this disease.

Ethical DisclosuresProtection of human and animal subjects

The authors declare that no experiments were performed on humans or animals for this study.

Confidentiality of data

The authors declare that they have followed the protocols of their work center on the publication of patient data.

Right to privacy and informed consent

The authors have obtained the written informed consent of the patients or subjects mentioned in the article. The corresponding author is in possession of this document.

Funding

The work for the present study was partially financed by a grant from SORCOM-MSD.

Conflicts of Interest

The authors declare they have no conflicts of interest.

Acknowledgments

To the Board of Directors of SORCOM, and especially to Santos Castañeda and Ana Cruz, for their unconditional support and commitment to this project; to Loreto Carmona for her advice and guidance in the methodology; and to the SER for its logistic support for the meetings of our group.

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Please cite this article as: Nuño L, Joven B, Carreira P, Maldonado V, Larena C, Llorente I, et al. Registro de pacientes con miopatía inflamatoria de la Sociedad Madrileña de Reumatología: análisis descriptivo. Reumatol Clin. 2017;13:331–337.

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