Long-Term Outcomes and Prognosis Factors in Patients With Idiopathic Inflammatory Myopathies Based on Myositis-Specific Autoantibodies: A Single Cohort Study

被引:15
|
作者
Jiang, Wei [1 ]
Shi, Jingli [1 ]
Yang, Hongxia [1 ]
Tian, Xiaolan [1 ]
Yang, Hanbo [1 ]
Chen, Qingning [1 ]
Zhang, Lining [1 ]
Peng, Qinglin [1 ]
Wang, Guochun [1 ]
Lu, Xin [1 ]
机构
[1] China Japan Friendship Hosp, Beijing, Peoples R China
关键词
INTERSTITIAL LUNG-DISEASE; GENE; 5; JAPANESE PATIENTS; CLINICAL-FEATURES; DERMATOMYOSITIS; COMPLICATION; POLYMYOSITIS; ASSOCIATION; MORTALITY; SURVIVAL;
D O I
10.1002/acr.24993
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveThis study was undertaken to investigate the long-term survival rates and prognostic factors in patients with idiopathic inflammatory myopathies (IIMs) based on myositis-specific antibody (MSA) stratification.MethodsExactly 628 patients with an IIM were included. Kaplan-Meier survival curves, univariate, and multivariate Cox regression were used to analyze the outcomes and risk factors.ResultsThe cumulative 1-, 5-, and 10-year survival rates for IIM patients overall were 91.4%, 82.8%, and 75.6%, respectively. The survival rate in the MSA subset was significantly different (P < 0.001). The 1- and 10-year survival rates in the anti-melanoma differentiation-associated protein 5 (anti-MDA-5)-positive subgroup were 79.5% and 58.5%, respectively, which were the lowest among all subgroups. The 10-year survival rate of anti-signal recognition particle (anti-SRP)-positive patients was the highest (96.4%). Independent risk factors that impacted the long-term prognosis for IIM patients included rapidly progressive interstitial lung disease (RP-ILD), malignancy, and elevated serum ferritin levels (hazard ratio [HR] 17.47, 20.36, and 9.15, respectively, P < 0.01), whereas disease duration was a protective factor (HR 0.27, P = 0.003). Among these subsets, the strongest independent risk factor for death in the anti-MDA-5-positive subgroup was RP-ILD (HR 3.4, P = 0.017). Malignancy was an independent risk factor in the anti-aminoacyl-tRNA synthetase antibody-positive, anti-transcription intermediary factor 1 gamma-positive, and MSA-negative subgroups (HR 46.69, 6.65, and 4.48, respectively; P < 0.001). RP-ILD was also a risk factor in the prognosis of individuals in the MSA-negative subgroup (HR 72.28, P < 0.001).ConclusionDespite favorable overall survival in patients with IIM, the anti-MDA-5-positive subgroup had the highest mortality rate among all MSA subgroups, highlighting the distinctive prognosis for patients with different MSAs. RP-ILD and malignancy are the most common causes of death in IIM patients.
引用
收藏
页码:1175 / 1182
页数:8
相关论文
共 50 条
  • [1] Clinical impact of myositis-specific autoantibodies on long-term prognosis of juvenile idiopathic inflammatory myopathies: multicentre study
    Yamasaki, Yuichi
    Kobayashi, Norimoto
    Akioka, Shinji
    Yamazaki, Kazuko
    Takezaki, Shunichiro
    Nakaseko, Haruna
    Ohara, Asami
    Nishimura, Kenichi
    Nishida, Yutaka
    Sato, Satoshi
    Kishi, Takayuki
    Hashimoto, Motomu
    Mori, Masaaki
    Okazaki, Yuka
    Kuwana, Masataka
    Ohta, Akiko
    RHEUMATOLOGY, 2021, 60 (10) : 4821 - 4831
  • [2] Long-term outcomes in 50 patients with idiopathic inflammatory myopathies (IIM) and role of myositis-specific antibodies
    Ferraro, M.
    Bortolani, S.
    Gadaleta, G.
    Rolle, E.
    Brusa, C.
    Vacchetti, M.
    Mongini, T. E.
    EUROPEAN JOURNAL OF NEUROLOGY, 2020, 27 : 219 - 219
  • [3] Myositis-specific autoantibodies in Japanese patients with juvenile idiopathic inflammatory myopathies
    Ueki, Masahiro
    Kobayashi, Ichiro
    Takezaki, Shunichiro
    Tozawa, Yusuke
    Okura, Yuka
    Yamada, Masafumi
    Kuwana, Masataka
    Ariga, Tadashi
    MODERN RHEUMATOLOGY, 2019, 29 (02) : 351 - 356
  • [4] Myositis-specific autoantibodies and their clinical associations in idiopathic inflammatory myopathies
    Wong, Victor Tak-Lung
    So, Ho
    Lam, Tommy Tsz-On
    Yip, Ronald Man-Lung
    ACTA NEUROLOGICA SCANDINAVICA, 2021, 143 (02): : 131 - 139
  • [5] Characteristics of idiopathic inflammatory myopathies with novel myositis-specific autoantibodies
    Rams, Anna
    Kosalka-Wegiel, Joanna
    Kuszmiersz, Piotr
    Matyja-Bednarczyk, Aleksandra
    Polanski, Stanislaw
    Zareba, Lech
    Bazan-Socha, Stanislawa
    ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, 2021, 30 (12): : 1239 - 1247
  • [6] Association between periungual changes and myositis-specific autoantibodies in patients with idiopathic inflammatory myopathies: A retrospective cohort study
    Ueda-Hayakawa, Ikuko
    Maekawa, Aya
    Tonomura, Kyoko
    Kaneda, Emi
    Yamazaki, Yuriko
    Arase, Noriko
    Fujimoto, Manabu
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2024, 91 (03) : 531 - 533
  • [7] The spectrum and clinical significance of myositis-specific autoantibodies in Chinese patients with idiopathic inflammatory myopathies
    Shanshan Li
    Yongpeng Ge
    Hanbo Yang
    Tao Wang
    Xiaoxiao Zheng
    Qinglin Peng
    Xin Lu
    Guochun Wang
    Clinical Rheumatology, 2019, 38 : 2171 - 2179
  • [8] The spectrum and clinical significance of myositis-specific autoantibodies in Chinese patients with idiopathic inflammatory myopathies
    Li, Shanshan
    Ge, Yongpeng
    Yang, Hanbo
    Wang, Tao
    Zheng, Xiaoxiao
    Peng, Qinglin
    Lu, Xin
    Wang, Guochun
    CLINICAL RHEUMATOLOGY, 2019, 38 (08) : 2171 - 2179
  • [9] The association between myositis-specific autoantibodies and muscle pathologies in idiopathic inflammatory myopathies
    Qiu Xu
    Qiu-Xiang Li
    Fang-Fang Bi
    Hui-Qian Duan
    Yue-Bei Luo
    Huan Yang
    Clinical Rheumatology, 2021, 40 : 613 - 624
  • [10] The association between myositis-specific autoantibodies and muscle pathologies in idiopathic inflammatory myopathies
    Xu, Qiu
    Li, Qiu-Xiang
    Bi, Fang-Fang
    Duan, Hui-Qian
    Luo, Yue-Bei
    Yang, Huan
    CLINICAL RHEUMATOLOGY, 2021, 40 (02) : 613 - 624