Clinical characteristics and prognostic factor in juvenile dermatomyositis: data of the Spanish registry

IF 2.8 3区 医学 Q1 PEDIATRICS
Sonia Carriquí-Arenas, Juan Manuel Mosquera, Estefanía Quesada-Masachs, Mireia López, Daniel Clemente, Alina Boteanu, Clara Udaondo, Jaime de Inocencio, Juan Carlos Nieto, Leyre Riancho, Esmeralda Núñez, Judith Sánchez-Manubens, María José Lirola, Rosa Roldán, Marisol Camacho, Melania Martínez, Marta Medrano, Paula Alcañiz, Jordi Antón, Estíbaliz Iglesias
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Abstract

Juvenile Dermatomyositis (JDM) is the most common chronic idiopathic inflammatory myopathy in children. The diagnosis is clinical. Baseline laboratory and complementary studies trace the phenotype of these patients. The objective of this study was to describe epidemiological, clinical and laboratory characteristics at diagnosis of JDM patients included in the Spanish JDM registry, as well as to identify prognostic factors on these patients. We retrospectively reviewed clinical features, laboratory tests, and complementary studies at diagnosis of JDM patients included on the Spanish JDM registry. These data were analyzed to assess whether there was a relationship with the development of complications and time to disease inactivity. One hundred and sixteen patients from 17 Spanish paediatric rheumatology centres were included, 76 girls (65%). Median age at diagnosis was 7.3 years (Interquartile range (IQR) 4.5–10.2). All patients had pathognomonic skin lesions at the beginning of the disease. Muscle weakness was present in 86.2%. Median Childhood Muscle Assessment Scale was 34 (IQR 22–47). Twelve patients (34%) had dysphagia and 3,5% dysphonia. Anti-p155 was the most frequently detected myositis specific antibody, followed by anti-MDA5. Twenty-nine patients developed calcinosis and 4 presented with macrophage activation syndrome. 70% reached inactivity in a median time of 8.9 months (IQR 4.5–34.8). 41% relapsed after a median time of 14.4 months (IQR 8.6–22.8) of inactivity. Shorter time to treatment was associated with better prognosis (Hazard ratio (HR) = 0.95 per month of evolution, p = 0.02). Heliotrope rash at diagnosis correlates with higher risk of development complications. We describe heliotrope rash as a risk factor for developing complications in our cohort of JDM patients, an easy-to-evaluate clinical sign that could help us to identify the group of patients we should monitor closely for this complication.
幼年皮肌炎的临床特征和预后因素:西班牙登记数据
幼年皮肌炎(JDM)是儿童中最常见的慢性特发性炎症性肌病。其诊断依据是临床表现。基线实验室和辅助研究可追踪这些患者的表型。本研究的目的是描述西班牙 JDM 登记处纳入的 JDM 患者诊断时的流行病学、临床和实验室特征,并确定这些患者的预后因素。我们回顾性审查了西班牙 JDM 登记处收录的 JDM 患者诊断时的临床特征、实验室检查和辅助研究。我们对这些数据进行了分析,以评估并发症的发生与疾病静止时间之间是否存在关系。西班牙17家儿科风湿病中心共纳入了116名患者,其中76名为女孩(占65%)。确诊时的中位年龄为 7.3 岁(四分位距(IQR)为 4.5-10.2)。所有患者在发病初期都有明显的皮肤损害。86.2%的患者存在肌肉无力。儿童肌肉评估量表中位数为34(IQR 22-47)。12名患者(34%)有吞咽困难,3.5%有发音障碍。抗p155是最常检测到的肌炎特异性抗体,其次是抗MDA5。29 名患者出现钙化,4 名患者出现巨噬细胞活化综合征。70%的患者在8.9个月(IQR 4.5-34.8)的中位时间内失去活动能力。41%的患者在中位 14.4 个月(IQR 8.6-22.8)的无效治疗后复发。较短的治疗时间与较好的预后有关(危险比 (HR) = 0.95/月,P = 0.02)。确诊时的日光疹与较高的并发症发生风险相关。我们将日光疹描述为JDM患者群中出现并发症的一个风险因素,这一易于评估的临床表现可帮助我们确定哪些患者应密切关注这一并发症。
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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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