Clinical Characteristics and Risk Factors of Polymyositis and Dermatomyositis Combined with Interstitial Lung Disease in Patients Residing in the Northeast Sichuan Province of China

Author:

Li Tao1,Tang Zi-Yi2,Zhang Quan-Bo1,Xiao Fan-Ni1,Jian Gui-Lin1,Xie Yan1,Guo Jian-Wei1,Qing Yu-Feng2

Affiliation:

1. Department of Geriatrics, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, China

2. Department of Rheumatology and Immunology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, China

Abstract

Background:: Polymyositis (PM) and dermatomyositis (DM) are non-suppurative and autoimmune inflammatory diseases of striated muscle. Interstitial lung disease (ILD) is a group of heterogeneous diseases that mainly involve the pulmonary interstitium, alveoli, and/or bronchioles, also known as diffuse parenchymal lung disease (DPLD). A significant cause of death in persons with polymyositis (PM) and dermatomyositis (DM) is concurrent interstitial lung disease (ILD). However, research on the clinical characteristics and associated influencing factors of PM/DM combined with ILD (PM/DM-ILD) is currently scarce in China. Objective:: The study aimed to probe the clinical features and risk factors of PM/DM-ILD. Methods:: The data of 130 patients with PM/DM were gathered. General medical status, clinical symptoms, laboratory parameters, high-resolution CT, therapeutic outcomes, and prognoses were retrospectively reviewed in patients with PM/DM with (ILD group) and without (NILD) ILD. Results:: The age of the ILD group (n=65) was more than the NILD group (n=65), and the differ-ence was statistically significant; there were no significant between-group variations in the PM/DM ratio, sex, or duration of the disease. The initial symptoms were arthritis and respiratory symptoms in the ILD group, and myasthenia symptoms in the NILD group. Incidences of Raynaud’s phenom-enon, dry cough, expectoration, dyspnea on exertion, arthritis, fever, total globulin (GLOB), eryth-rocyte sedimentation rate (ESR), and anti-Jo-1 antibody rate were higher for ILD; however, albumin (ALB), creatine kinase aspartate aminotransferase activity ratio (CK/AST) and CK levels were sig-nificantly lower in the ILD group. Bivariate logistic regression analysis showed age, dry cough, ar-thritis, dyspnea on exertion, anti-Jo-1 antibody, and elevated GLOB to be independent risk factors for ILD among patients with PM/DM. Conclusion:: Advanced age, dry cough, arthritis, dyspnea on exertion, anti-Jo-1 antibody positivity, and elevated GLOB level are risk factors for PM/DM-ILD. This information could be utilized to carefully monitor changing lung function in these patients.

Funder

National Natural Science Foundation of China

Post- Doctorate Research Project, West China Hospital, Sichuan University

Publisher

Bentham Science Publishers Ltd.

Subject

Rheumatology

Reference22 articles.

1. Lega J.C.; Reynaud Q.; Belot A.; Fabien N.; Durieu I.; Cottin V.; Idiopathic inflammatory myopathies and the lung. Eur Respir Rev 2015,24(136),216-238

2. Bohan A.; Peter J.B.; Polymyositis and dermatomyositis. N Engl J Med 1975,292(7),344-347

3. Chinese Rheumatic Disease Data Center. 2018 Chinese expert-based consensus statement regarding the diagnosis and treatment of interstitial lung disease associated with connective tissue diseases. Zhonghua Nei Ke Za Zhi Group of Pulmonary Vascular and Interstitial Diseases Associated with Rheumatic Diseases, Chinese Association of Rheumatology and Immunology Physicians2018,57(8),558-565

4. Ha Y.J.; Lee Y.J.; Kang E.H.; Lung involvements in rheumatic diseases: Update on the epidemiology, pathogenesis, clinical features, and treatment. BioMed Res Int 2018,2018,1-19

5. Johnson C.; Rosen P.; Lloyd T.; Exploration of the MUC5B promoter variant and ILD risk in patients with autoimmune myositis. Respir Med 2017,130,52-54

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3