Clinical subsets associated with different anti-aminoacyl transfer RNA synthetase antibodies and their association with coexisting anti-Ro52

Objective: To characterize clinical features of polymyositis/dermatomyositis (PM/DM) patients with different anti-aminoacyl transfer RNA synthetase (ARS) antibodies and their association with anti-Ro52. Methods: Autoantibodies in sera from 97 Japanese patients (36 PM, 56 DM, and 5 clinically amyopat...

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Veröffentlicht in:Modern rheumatology 2016-01, Vol.26 (3), p.403-409
Hauptverfasser: Yamasaki, Yoshioki, Satoh, Minoru, Mizushima, Machiko, Okazaki, Takahiro, Nagafuchi, Hiroko, Ooka, Seido, Shibata, Tomohiko, Nakano, Hiromasa, Ogawa, Hitoshi, Azuma, Kohei, Maeda, Akihiko, Tonooka, Kumiko, Ito, Hiroshi, Takakuwa, Yukiko, Inoue, Makoto, Mitomi, Hirofumi, Kiyokawa, Tomofumi, Tsuchida, Kosei, Matsushita, Hiromi, Mikage, Hidenori, Murakami, Yoshihiko, Chan, Jason Y. F., Ozaki, Shoichi, Yamada, Hidehiro
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Sprache:eng
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Zusammenfassung:Objective: To characterize clinical features of polymyositis/dermatomyositis (PM/DM) patients with different anti-aminoacyl transfer RNA synthetase (ARS) antibodies and their association with anti-Ro52. Methods: Autoantibodies in sera from 97 Japanese patients (36 PM, 56 DM, and 5 clinically amyopathic DM), who satisfied Bohan and Peter or modified Sontheimer's criteria, were characterized by immunoprecipitation and enzyme-linked immunosorbent assay. Clinical information was from medical records. Features associated with different anti-ARS and anti-Ro52 antibodies were analyzed. Results: The prevalence of anti-ARS was similar to other studies (Jo-1, 22%; EJ, 4%; OJ, 1%; PL-12, 1%), except for a high prevalence of anti-PL-7 (12%), which allowed us to characterize patients carrying this specificity. Serum creatine kinase >3000 IU/l was less common in anti-PL-7-positive patients (57%) than anti-Jo-1-positive patients (18%) (p = 0.0328) and was not found in anti-EJ-positive individuals. Interstitial lung disease was common in anti-ARS-positive patients (97%) (p 
ISSN:1439-7595
1439-7609
DOI:10.3109/14397595.2015.1091155