Sallum Adriana M E, Pivato Francine C M M, Doria-Filho Ulysses, Aikawa Nádia E, Liphaus Bernadete L, Marie Suely K N, Silva Clovis A A
Departamento de Pediatria, Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
J Pediatr (Rio J). 2008 Jan-Feb;84(1):68-74. doi: 10.2223/JPED.1746. Epub 2008 Jan 9.
To identify risk factors associated with calcinosis in children and adolescents with juvenile dermatomyositis.
A review was carried out of the medical records of 54 patients with juvenile dermatomyositis. Data were collected on demographic characteristics, clinical features: muscle strength (stages I to V of the Medical Research Council scale), pulmonary involvement (restrictive pulmonary disease with presence or absence of anti-Jo1 antibodies), gastrointestinal problems (gastroesophageal reflux) and/or heart disease (pericarditis and/or myocarditis); laboratory tests: elevated muscle enzyme levels in serum (creatine phosphokinase, aspartate aminotransferase, alanine aminotransferase and/or lactate dehydrogenase); and on the treatments given: corticoid therapy in isolation or associated with hydroxychloroquine and/or immunosuppressants. The patients were divided into two groups, depending on presence or absence of calcinosis and data were evaluated by both univariate and multivariate analyses.
Calcinosis was identified in 23 (43%) patients, and in six (26%) patients it had emerged prior to diagnosis while in 17 (74%) it was post diagnosis. The univariate analysis revealed that cardiac (p = 0.01) and pulmonary (p = 0.02) involvement and the need for one or more immunosuppressor (methotrexate, cyclosporine A and/or pulse therapy with intravenous cyclophosphamide) to treat juvenile dermatomyositis (p = 0.03) were all associated with an increased incidence of calcinosis. The multivariate analysis then demonstrated that only cardiac involvement (OR = 15.56; 95%CI 1.59-152.2) and the use of one or more immunosuppressor (OR = 4.01; 95%CI 1.08-14.87) were independently associated with the presence of calcinosis.
Calcinosis was a frequent development among these juvenile dermatomyositis cases, generally emerging as the disease progressed. Calcinosis was associated with the more severe cases that also had cardiac involvement and where immunosuppressors had to be included in the treatment.
确定青少年皮肌炎患儿和青少年发生钙质沉着症的相关危险因素。
对54例青少年皮肌炎患者的病历进行回顾。收集以下数据:人口统计学特征、临床特征(肌肉力量,采用医学研究委员会量表的I至V级)、肺部受累情况(存在或不存在抗Jo1抗体的限制性肺病)、胃肠道问题(胃食管反流)和/或心脏病(心包炎和/或心肌炎);实验室检查(血清中肌肉酶水平升高,如肌酸磷酸激酶、天冬氨酸转氨酶、丙氨酸转氨酶和/或乳酸脱氢酶);以及所给予的治疗(单独使用皮质类固醇治疗或与羟氯喹和/或免疫抑制剂联合使用)。根据是否存在钙质沉着症将患者分为两组,并通过单因素和多因素分析对数据进行评估。
23例(43%)患者出现钙质沉着症,其中6例(26%)在诊断前出现,17例(74%)在诊断后出现。单因素分析显示,心脏受累(p = 0.01)、肺部受累(p = 0.02)以及治疗青少年皮肌炎时需要使用一种或多种免疫抑制剂(甲氨蝶呤、环孢素A和/或静脉注射环磷酰胺进行脉冲治疗)(p = 0.03)均与钙质沉着症发生率增加相关。多因素分析表明,只有心脏受累(比值比=15.56;95%置信区间1.59 - 152.2)和使用一种或多种免疫抑制剂(比值比=4.01;95%置信区间1.08 - 14.87)与钙质沉着症的存在独立相关。
在这些青少年皮肌炎病例中,钙质沉着症是一种常见的病情发展情况,通常随着疾病进展而出现。钙质沉着症与病情更严重的病例相关,这些病例同时伴有心脏受累且治疗中必须使用免疫抑制剂。