VA Nebraska-Western IA Health Care System, Omaha, NE, USA.
Division of Rheumatology and Immunology, Department of Internal Medicine, University of Nebraska Medical Center, 986270 Nebraska Med Center, Omaha, Nebraska, United States.
Clin Rheumatol. 2018 Nov;37(11):2907-2915. doi: 10.1007/s10067-018-4314-9. Epub 2018 Oct 2.
Assess the impact of chronic lung diseases (CLD) on survival in rheumatoid arthritis (RA). Among participants in the Veterans Affairs Rheumatoid Arthritis (VARA) Registry, a prospective cohort of U.S. Veterans with RA, we identified CLD and cardiovascular disease (CVD) using administrative and registry data. Demographics, smoking status, RA characteristics including Disease Activity Score in 28 joints (DAS28), and disease-modifying anti-rheumatic drug (DMARD) use were obtained from registry data, which were linked to the National Death Index to obtain vital status. We evaluated associations of CLD with survival using the multivariable Cox regression models. Among a large (n = 2053), male-predominant (91%) RA cohort, 554 (27%) had CLD at enrollment. Mortality risk was increased 1.51-fold (95% CI 1.26-1.81) in RA patients with CLD after multivariable adjustment, a risk that was similar to that observed with CVD (HR CLD alone 1.46 [1.03-2.06]; CVD alone 1.62 [1.35-1.94]). Survival was significantly reduced in those with interstitial lung disease (ILD) as well as other forms of CLD. Mortality risk with methotrexate and biologic use was not different in those with CLD compared to those without (p interaction ≥ 0.15) using multiple exposure definitions and propensity score adjustment. Mortality risk is significantly increased in RA patients with CLD. This risk is attributable not only to ILD but also to other chronic lung conditions and does not appear to be substantially greater in those receiving methotrexate or biologic therapies. Comorbid lung disease should be targeted as a means of improving long-term outcomes in RA.
评估慢性肺部疾病(CLD)对类风湿关节炎(RA)患者生存的影响。在退伍军人事务部类风湿关节炎(VARA)注册中心,一个美国退伍军人类风湿关节炎的前瞻性队列中,我们使用行政和注册数据确定了 CLD 和心血管疾病(CVD)。从注册数据中获得了人口统计学、吸烟状况、RA 特征,包括 28 个关节疾病活动评分(DAS28)和疾病修饰抗风湿药物(DMARD)的使用情况,这些数据与国家死亡索引相关联,以获取生存状况。我们使用多变量 Cox 回归模型评估 CLD 与生存的相关性。在一个大型(n=2053)、男性为主(91%)的 RA 队列中,554 名(27%)患者在入组时患有 CLD。多变量调整后,RA 患者 CLD 组的死亡率风险增加了 1.51 倍(95%CI 1.26-1.81),与 CVD 观察到的风险相似(CLD 单独的 HR 1.46[1.03-2.06];CVD 单独的 HR 1.62[1.35-1.94])。患有间质性肺病(ILD)和其他形式的 CLD 的患者生存时间明显缩短。使用多种暴露定义和倾向评分调整后,与没有 CLD 的患者相比,CLD 患者使用甲氨蝶呤和生物制剂的死亡率风险没有差异(p 交互≥0.15)。RA 患者 CLD 死亡率风险显著增加。这种风险不仅归因于ILD,还归因于其他慢性肺部疾病,而且在接受甲氨蝶呤或生物治疗的患者中,这种风险似乎并没有显著增加。合并肺部疾病应作为改善 RA 患者长期预后的一种手段。