Differential clinical features of patients with clinically amyopathic dermatomyositis who have circulating anti-MDA5 autoantibodies with or without myositis-associated autoantibodies

Anti-melanoma differentiation-associated gene 5 (MDA5) autoantibodies have been identified as myositis-specific autoantibodies that are often associated with clinically amyopathic dermatomyositis (CADM) and a poor prognosis due to rapidly progressive interstitial lung disease (RP-ILD) in East Asian...

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Veröffentlicht in:Respiratory medicine 2018-07, Vol.140, p.1-5
Hauptverfasser: Yamaguchi, Koichi, Yamaguchi, Aya, Kashiwagi, Chiharu, Sawada, Yuri, Taguchi, Kohei, Umetsu, Kazue, Oshima, Kazuma, Uchida, Megumi, Suzuki, Masafumi, Kono, Shunichi, Takemura, Masao, Masubuchi, Hiroaki, Kitahara, Shinsuke, Hara, Kenichiro, Maeno, Toshitaka, Motegi, Sei-ichiro, Muro, Yoshinao, Sakairi, Toru, Hisada, Takeshi, Kurabayashi, Masahiko
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Sprache:eng
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Zusammenfassung:Anti-melanoma differentiation-associated gene 5 (MDA5) autoantibodies have been identified as myositis-specific autoantibodies that are often associated with clinically amyopathic dermatomyositis (CADM) and a poor prognosis due to rapidly progressive interstitial lung disease (RP-ILD) in East Asian patients. Besides anti-MDA5 autoantibodies, patients with CADM may have myositis-associated autoantibodies (MAAs), which characterize other connective tissue diseases such as rheumatoid arthritis and Sjögren's syndrome. However, the clinical significance of the coexistence of anti-MDA5 autoantibodies and MAAs in patients with CADM remains unclear. We retrospectively analyzed 24 patients with CADM who had anti-MDA5 autoantibodies. Their clinical phenotypes including laboratory test results, high-resolution lung computed tomography data, response to therapy, and prognosis were compared between those who were positive and negative for MAAs, such as antinuclear antibody (ANA), anti-cyclic citrullinated peptide (CCP), anti-SSA, and anti-SSB antibodies. Among 24 patients, 9 (37.5%) additionally had at least one of the MAAs examined in this study: 1 patient was positive for ANA, 5 for anti-CCP, 5 for either anti-SSA or anti-SSB, 1 for anti-cardiolipin, and 1 for anti-Scl-70. Although all anti-MDA5-positive patients with CADM had ILD, the MAA-positive patients showed a lower risk of developing RP-ILD (p = 0.03), a more favorable response to combination therapy of corticosteroids and immunosuppressive agents, and a lower mortality rate than patients with no MAAs (p = 0.03). Our data suggest that anti-MDA5-positive patients with CADM who also have MAAs have a better prognosis than those without MAAs; thus, anti-MDA5 autoantibodies by themselves may not be strong predictors of worse clinical outcomes in patients with CADM. Coexistent MAAs could be biomarkers for a favorable prognosis in anti-MDA5-positive patients with CADM. •MAA-positive patients had a lower risk of developing RP-ILD.•Immunosuppressive treatment was effective for MAA-positive patients with RP-ILD.•MAAs may serve as a favorable prognostic marker for MDA5-positive CADM patients.
ISSN:0954-6111
1532-3064
DOI:10.1016/j.rmed.2018.05.010