抗炎与抗纤维化治疗类风湿关节炎相关间质性肺疾病:系统评价和荟萃分析方案

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES
Sneh Sonaiya, Alexandra Jianu, Nicholas Jianu, Kavita Batra
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引用次数: 0

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,影响美国和北欧约0.5%至1%的人口。间质性肺疾病(ILD)是RA最常见、最严重的肺部表现,统称RA相关性ILD (RA-ILD)。RA-ILD对发病率和死亡率有显著的影响,通常表现为不同的临床病程。尽管皮质类固醇和改善疾病的抗风湿药物(DMARDs)仍然是RA治疗的基石,但它们在RA- ild中的作用尚不明确。相反,抗纤维化疗法,如吡非尼酮和尼达尼布,最初是为特发性肺纤维化而开发的,现在正在探索其治疗RA-ILD纤维化变体的潜力。尽管临床应用越来越多,但尚无系统综述全面比较抗纤维化与抗炎治疗在慢性RA-ILD中的安全性和有效性。目的:本研究旨在比较抗纤维化和抗炎治疗对慢性RA-ILD患者肺功能、放射学进展、临床结局和安全性的影响。方法:本研究遵循PRISMA(首选报告项目用于系统评价和荟萃分析)指南,并在PROSPERO注册(CRD42024583847)。将对PubMed、Embase和Cochrane图书馆进行全面搜索,查找1991年1月至2024年8月之间发表的研究。符合条件的研究将包括根据放射学或组织病理学结果诊断为RA并证实为ILD的成人患者(年龄≥18岁),这些患者已接受抗纤维化或抗炎治疗。PECOS(人群、暴露、比较者、结果、研究设计)框架将用于确定纳入标准。本综述评估的主要结局将包括以下肺功能参数:用力肺活量、1秒用力呼气量和肺对一氧化碳的扩散能力。抗炎治疗将分为皮质类固醇、常规合成dmard和生物dmard,以解释异质性。将使用Cochrane偏倚风险2 (RoB 2)和非随机干预研究偏倚风险(ROBINS-I)工具进行质量评估,并使用GRADE(分级推荐评估、发展和评价)方法评估证据的确定性。结果:文献检索筛选于2024年8月开始,数据提取正在进行中。最终结果预计将于2025年12月公布。结论:本系统综述和荟萃分析将提供抗纤维化和抗炎治疗慢性RA-ILD的全面比较。这些发现将有助于为临床决策提供信息,支持基于证据的治疗选择,并确定当前研究中的差距。通过解决疗效和安全性,本综述旨在指导未来的研究并改善这种复杂和衰弱性疾病的患者预后。试验注册:PROSPERO CRD42024583847;https://www.crd.york.ac.uk/PROSPERO/view/CRD42024583847.International注册报告标识符(irrid): DERR1-10.2196/73219。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Inflammatory Versus Antifibrotic Therapies for the Management of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Protocol for a Systematic Review and Meta-Analysis.

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.

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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
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