Plasma Matrix Metalloproteinase Concentrations and Risk of Interstitial Lung Disease in a Prospective Rheumatoid Arthritis Cohort

医学 内科学 危险系数 间质性肺病 类风湿性关节炎 优势比 四分位数 前瞻性队列研究 队列 置信区间 队列研究 比例危险模型 入射(几何) 物理 光学
作者
Brent A. Luedders,Austin M. Wheeler,Dana P. Ascherman,Joshua F. Baker,Michael J. Duryee,Yangyuna Yang,Punyasha Roul,Katherine D. Wysham,Paul A. Monach,Andreas Reimold,Gail S. Kerr,Gary Kunkel,Grant W. Cannon,Jill A. Poole,Geoffrey M. Thiele,Ted R. Mikuls,Bryant R. England
出处
期刊:Arthritis & rheumatology [Wiley]
被引量:13
标识
DOI:10.1002/art.42812
摘要

Objective To evaluate the associations of plasma matrix metalloproteinases (MMPs) with prevalent and incident interstitial lung disease (ILD) in people with rheumatoid arthritis (RA). Methods Within a multicenter, prospective cohort of US veterans with RA, we performed a cross‐sectional study of prevalent ILD and cohort study of incident ILD. ILD diagnoses were validated by medical record review of provider diagnoses and chest imaging and/or pathology reports. MMP‐1, 3, 7, and 9 concentrations were measured in plasma samples, then standardized and categorized into quartiles. The associations of MMPs with prevalent and incident ILD were assessed with logistic (prevalent) and Cox (incident) regression models adjusted for RA‐ILD risk factors. Results Among 2,312 participants (88.9% male; mean age 63.8 years), 96 had prevalent ILD. Incident ILD developed in 130 participants over 17,378 person‐years of follow‐up (crude incidence rate 7.5/1,000 person‐years). Participants with the highest quartile of MMP‐7 concentrations had a nearly four‐fold increased odds of prevalent ILD (adjusted odds ratio 3.78 [95% confidence interval (95% CI) 1.86–7.65]) and over two‐fold increased risk of incident ILD (adjusted hazard ratio 2.33 [95% CI 1.35–4.02]). Higher MMP‐9 concentrations were also associated with prevalent and incident ILD, as well as negatively correlated with forced vital capacity among those with prevalent ILD ( r = −0.30, P = 0.005). Conclusion MMP‐7 and MMP‐9 were strongly associated with both prevalent and incident ILD in this large, multicenter RA cohort after adjustment for other RA‐ILD risk factors. These population‐level findings further support a potential pathogenic role for MMPs in RA‐ILD and suggest that their measurement could facilitate RA‐ILD risk stratification.

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