The diagnostic utility of anti-melanoma differentiation-associated gene 5 antibody testing for predicting the prognosis of Japanese patients with DM

医学 内科学 危险系数 胃肠病学 MDA5型 间质性肺病 黑色素瘤 抗体 比例危险模型 皮肌炎 呼吸衰竭 免疫学 基因 癌症研究 置信区间 RNA干扰 化学 核糖核酸 生物化学
作者
Tomohiro Koga,Keita Fujikawa,Yoshiro Horai,Akira Okada,Shin‐ya Kawashiri,Noriyuki Iwamoto,Takahisa Suzuki,Yoshikazu Nakashima,Mami Tamai,Kazuhiko Arima,Satoshi Yamasaki,Hidetoshi Nakamura,Tomoki Origuchi,Y. Hamaguchi,Manabu Fujimoto,Yuji Ishimatsu,Hiroshi Mukae,Masataka Kuwana,S Kohno,Katsumi Eguchi
出处
期刊:Rheumatology [Oxford University Press]
卷期号:51 (7): 1278-1284 被引量:316
标识
DOI:10.1093/rheumatology/ker518
摘要

OBJECTIVE: Interstitial lung disease (ILD), especially rapidly progressive ILD (RPILD), is a major poor prognostic factor in patients with DM. We investigated the association of anti-melanoma differentiation-associated gene 5 (MDA5) antibody (Ab) with clinical characteristics and mortality in Japanese patients with DM. METHODS: Seventy-nine DM patients, comprising 58 classic DM and 21 clinically amyopathic DM (CADM) patients, were enrolled. Serum Abs were screened by immunoprecipitation assays, and an immunosorbent assay (ELISA) was used for MDA5. The relationships of clinical characteristics and mortality with each Ab were investigated. RESULTS: Anti-MDA5 Ab was detected in 17 patients. Anti-clinically amyopathic DM 140 kDa polypeptide Abs (anti-CADM-140 Abs) were found in 16 of the 17 anti-MDA5 Ab(+) patients. Skin ulcers, palmar papules, CADM, RPILD and mediastinal emphysema were widely distributed in anti-MDA5 Ab(+) patients. Mortality at 6 months as well as 5 years was also significantly higher in anti-MDA5 Ab(+) patients than in anti-MDA5 Ab(-) patients. In a multivariable Cox regression analysis, mortality was independently associated with anti-MDA5 Ab (relative hazard 6.33; 95% CI 1.43, 28.0). All of the deaths in anti-MDA5 Ab(+) patients were attributed to respiratory failure of RPILD; however, RPILD did not worsen in any of the anti-MDA5 Ab(+) patients who survived the first 6 months. CONCLUSION: The presence of anti-MDA5 Ab identifies the characteristic skin, musculoskeletal, pulmonary and prognostic features in patients with DM. In addition, anti-MDA5 Ab seems to predict a group of patients with CADM-complicated fatal RPILD.
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