特发性炎性肌病间质性肺疾病的生物标志物和自身抗体。

IF 1 Q4 RESPIRATORY SYSTEM Clinical Medicine Insights-Circulatory Respiratory and Pulmonary Medicine Pub Date : 2016-04-03 eCollection Date: 2015-01-01 DOI:10.4137/CCRPM.S36748
Hajime Yoshifuji
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引用次数: 14

摘要

特发性炎性肌病中可见多种自身抗体。在肌炎特异性抗体中,抗氨基酰基trna合成酶和抗黑色素瘤分化相关蛋白5 (MDA5)抗体与间质性肺疾病(ILD)相关。抗mda5抗体与皮肌炎(DM)或临床淀粉样病变DM合并快速进展性ILD相关。在抗mda5阳性患者中,随机磨玻璃衰减模式是胸部高分辨率计算机断层扫描的特征发现。相反,抗氨基酰基trna合成酶抗体与快速进展性ILD无关,但与慢性ILD相关。具有抗mda5和特征性高分辨率计算机断层扫描结果的糖尿病或临床淀粉样病变糖尿病患者极有可能患有破坏性ILD,需要积极治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Biomarkers and Autoantibodies of Interstitial Lung Disease with Idiopathic Inflammatory Myopathies.

Various autoantibodies are seen in idiopathic inflammatory myopathies. Among myositis-specific antibodies, anti-aminoacyl-tRNA synthetase and anti-melanoma differentiation-associated protein 5 (MDA5) antibodies are associated with interstitial lung disease (ILD). Anti-MDA5 antibodies are associated with dermatomyositis (DM) or clinically amyopathic DM complicated with rapidly progressive ILD. In anti-MDA5-positive patients, a random ground-glass attenuation pattern is a characteristic finding of ILD in chest high-resolution computed tomography. Conversely, anti-aminoacyl-tRNA synthetase antibodies are not associated with rapidly progressive ILD but with chronic ILD. DM or clinically amyopathic DM patients with anti-MDA5, and characteristic high-resolution computed tomography findings are highly likely to have devastating ILD and need aggressive treatment.

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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
9
审稿时长
8 weeks
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