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用于治疗类风湿关节炎相关间质性肺病的抗炎与抗纤维化疗法:系统评价与荟萃分析方案

Anti-Inflammatory Versus Antifibrotic Therapies for the Management of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Protocol for a Systematic Review and Meta-Analysis.

作者信息

Sonaiya Sneh, Jianu Alexandra, Jianu Nicholas, Batra Kavita

机构信息

Department of Internal Medicine, University of Nevada, Las Vegas, Las Vegas, NV, United States.

Department of Medicine, Lake Erie College of Osteopathic Medicine, Erie, PA, United States.

出版信息

JMIR Res Protoc. 2025 Jul 21;14:e73219. doi: 10.2196/73219.

Abstract

BACKGROUND

Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease that affects approximately 0.5% to 1% of the population in the United States and Northern Europe. Interstitial lung disease (ILD) is the most common and severe pulmonary manifestation of RA, collectively referred to as RA-associated ILD (RA-ILD). RA-ILD contributes significantly to morbidity and mortality and often presents with a variable clinical course. Although corticosteroids and disease-modifying antirheumatic drugs (DMARDs) remain the cornerstone of RA management, their role in RA-ILD is less clearly defined. In contrast, antifibrotic therapies such as pirfenidone and nintedanib, initially developed for idiopathic pulmonary fibrosis, are now being explored for their potential in treating fibrosing variants of RA-ILD. Despite increasing clinical use, no systematic review has comprehensively compared the safety and efficacy of antifibrotic versus anti-inflammatory therapies in chronic RA-ILD.

OBJECTIVE

This study aims to compare the impact of antifibrotic and anti-inflammatory therapies on lung function, radiologic progression, clinical outcomes, and safety in patients with chronic RA-ILD.

METHODS

This study will follow PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines and is registered with PROSPERO (CRD42024583847). A comprehensive search of PubMed, Embase, and the Cochrane Library will be conducted for studies published between January 1991 and August 2024. Eligible studies will include adult patients (aged ≥18 years) with a diagnosis of RA and confirmed ILD based on radiological or histopathological findings who have been treated with either antifibrotic or anti-inflammatory therapies. The PECOS (Population, Exposure, Comparator, Outcome, Study Design) framework will be used to define inclusion criteria. The primary outcomes assessed in this review will include the following pulmonary function parameters: forced vital capacity, forced expiratory volume in 1 second, and diffusing capacity of the lungs for carbon monoxide. Anti-inflammatory therapies will be stratified into corticosteroids, conventional synthetic DMARDs, and biologic DMARDs to account for heterogeneity. The Cochrane Risk of Bias 2 (RoB 2) and Risk of Bias in Non-randomized Studies - of Interventions (ROBINS-I) tools will be used for quality assessment, and GRADE (Grading of Recommendations Assessment, Development, and Evaluation) methodology will be used to evaluate the certainty of evidence.

RESULTS

The literature search and screening commenced in August 2024, and data extraction is underway. The final results are expected by December 2025.

CONCLUSIONS

This systematic review and meta-analysis will provide a comprehensive comparison of antifibrotic and anti-inflammatory therapies in the treatment of chronic RA-ILD. The findings will help inform clinical decision-making, support evidence-based treatment selection, and identify gaps in current research. By addressing both efficacy and safety, this review aims to guide future studies and improve patient outcomes for this complex and debilitating condition.

TRIAL REGISTRATION

PROSPERO CRD42024583847; https://www.crd.york.ac.uk/PROSPERO/view/CRD42024583847.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/73219.

摘要

背景

类风湿关节炎(RA)是一种慢性自身免疫性炎症性疾病,在美国和北欧约0.5%至1%的人口中受其影响。间质性肺疾病(ILD)是RA最常见且最严重的肺部表现,统称为RA相关ILD(RA-ILD)。RA-ILD对发病率和死亡率有显著影响,且临床病程多变。尽管皮质类固醇和改善病情抗风湿药(DMARDs)仍是RA治疗的基石,但其在RA-ILD中的作用尚不太明确。相比之下,最初用于特发性肺纤维化的抗纤维化疗法,如吡非尼酮和尼达尼布,目前正被探索用于治疗RA-ILD纤维化变体的潜力。尽管临床应用日益增多,但尚无系统评价全面比较抗纤维化疗法与抗炎疗法在慢性RA-ILD中的安全性和疗效。

目的

本研究旨在比较抗纤维化和抗炎疗法对慢性RA-ILD患者肺功能、影像学进展、临床结局和安全性的影响。

方法

本研究将遵循PRISMA(系统评价和Meta分析的首选报告项目)指南,并在PROSPERO(CRD42024583847)注册。将全面检索PubMed、Embase和Cochrane图书馆,查找1991年1月至2024年8月发表的研究。符合条件的研究将包括年龄≥18岁、诊断为RA且根据影像学或组织病理学结果确诊为ILD、接受过抗纤维化或抗炎疗法治疗的成年患者。将使用PECOS(人群、暴露、对照、结局、研究设计)框架来定义纳入标准。本评价中评估的主要结局将包括以下肺功能参数:用力肺活量、1秒用力呼气量和肺一氧化碳弥散量。抗炎疗法将分为皮质类固醇、传统合成DMARDs和生物DMARDs,以考虑异质性。将使用Cochrane偏倚风险2(RoB 2)和非随机研究中的干预偏倚风险(ROBINS-I)工具进行质量评估,并使用GRADE(推荐分级评估、制定和评价)方法评估证据的确定性。

结果

文献检索和筛选于2024年8月开始,数据提取正在进行中。预计最终结果将于2025年12月得出。

结论

本系统评价和Meta分析将全面比较抗纤维化和抗炎疗法在治疗慢性RA-ILD中的效果。研究结果将有助于指导临床决策,支持基于证据的治疗选择,并识别当前研究中的差距。通过兼顾疗效和安全性,本评价旨在指导未来研究并改善这种复杂且使人衰弱疾病的患者结局。

试验注册

PROSPERO CRD42024583847;https://www.crd.york.ac.uk/PROSPERO/view/CRD42024583847。

国际注册报告识别码(IRRID):DERR1-10.2196/73219。

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