ANCHOR-RA 的设计:一项关于类风湿关节炎患者间质性肺病筛查的多国横断面研究。

IF 2.1 Q3 RHEUMATOLOGY BMC Rheumatology Pub Date : 2024-05-21 DOI:10.1186/s41927-024-00389-4
Jeffrey A Sparks, Philippe Dieudé, Anna-Maria Hoffmann-Vold, Gerd R Burmester, Simon Lf Walsh, Michael Kreuter, Christian Stock, Steven Sambevski, Margarida Alves, Paul Emery
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引用次数: 0

摘要

背景:类风湿性关节炎(RA)患者有患间质性肺病(ILD)的风险,这种疾病与高死亡率相关。需要基于风险因素的筛查工具来决定哪些类风湿性关节炎患者应使用高分辨率计算机断层扫描(HRCT)进行间质性肺病筛查。ANCHOR-RA研究是一项多国横断面研究,它将建立一个预测RA-ILD的多变量模型,该模型可用于临床实践中的RA-ILD筛查:研究人员将连续招募具有以下 RA-ILD 风险因素中≥ 2 个因素的 RA 患者:男性;目前或曾经吸烟;确诊 RA 时年龄≥ 60 岁;类风湿因子和/或抗环瓜氨酸肽阳性率高(滴度 > 3 x 正常值上限);存在或曾有某些 RA 的关节外表现(血管炎、费尔蒂综合征、继发性斯约格伦综合征、皮肤类风湿结节、血清炎和/或巩膜炎/葡萄膜炎);前 12 个月 RA 疾病活动度高。之前被确认为患有 ILD 的患者或在过去两年中接受过 CT 扫描的患者将不符合条件。参与者将在当地接受 HRCT 扫描,并由两名放射科专家进行集中评估。将前瞻性地收集有关人口统计学和 RA 相关特征、患者报告结果、合并症和肺功能的数据。主要结果将是根据一个多变量模型,结合临床实践中通常评估的潜在风险因素,得出RA-ILD的概率分值,并估计RA-ILD在研究人群中的患病率。计划将在美国、英国、德国、法国、意大利和西班牙的约 30 个地点招募 1200 名参与者:ANCHOR-RA研究的数据将为支持RA-ILD筛查的建议提供更多证据,以提高对RA这一重要并发症的检出率,并实现早期干预。试验注册:clinicaltrials.gov NCT05855109(提交日期:2023年5月3日)。
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Design of ANCHOR-RA: a multi-national cross-sectional study on screening for interstitial lung disease in patients with rheumatoid arthritis.

Background: Patients with rheumatoid arthritis (RA) are at risk of developing interstitial lung disease (ILD), which is associated with high mortality. Screening tools based on risk factors are needed to decide which patients with RA should be screened for ILD using high-resolution computed tomography (HRCT). The ANCHOR-RA study is a multi-national cross-sectional study that will develop a multivariable model for prediction of RA-ILD, which can be used to inform screening for RA-ILD in clinical practice.

Methods: Investigators will enrol consecutive patients with RA who have ≥ 2 of the following risk factors for RA-ILD: male; current or previous smoker; age ≥ 60 years at RA diagnosis; high-positive rheumatoid factor and/or anti-cyclic citrullinated peptide (titre > 3 x upper limit of normal); presence or history of certain extra-articular manifestations of RA (vasculitis, Felty's syndrome, secondary Sjögren's syndrome, cutaneous rheumatoid nodules, serositis, and/or scleritis/uveitis); high RA disease activity in the prior 12 months. Patients previously identified as having ILD, or who have had a CT scan in the prior 2 years, will not be eligible. Participants will undergo an HRCT scan at their local site, which will be assessed centrally by two expert radiologists. Data will be collected prospectively on demographic and RA-related characteristics, patient-reported outcomes, comorbidities and pulmonary function. The primary outcomes will be the development of a probability score for RA-ILD, based on a multivariable model incorporating potential risk factors commonly assessed in clinical practice, and an estimate of the prevalence of RA-ILD in the study population. It is planned that 1200 participants will be enrolled at approximately 30 sites in the USA, UK, Germany, France, Italy, Spain.

Discussion: Data from the ANCHOR-RA study will add to the body of evidence to support recommendations for screening for RA-ILD to improve detection of this important complication of RA and enable early intervention.

Trial registration: clinicaltrials.gov NCT05855109 (submission date: 3 May 2023).

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来源期刊
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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