Ozen Gulsen, Dell'Aniello Sophie, Pedro Sofia, Michaud Kaleb, Suissa Samy
University of Nebraska Medical Center, Omaha.
Jewish General Hospital, Montreal, Quebec, Canada.
Arthritis Care Res (Hoboken). 2023 Mar;75(3):597-607. doi: 10.1002/acr.24866. Epub 2022 Nov 17.
To assess the effect of statin use on the risk of cardiovascular disease (CVD), all-cause mortality, and type 2 diabetes mellitus (DM) in patients with rheumatoid arthritis (RA).
We identified a cohort of patients with RA between 1989 and 2018, within the UK Clinical Practice Research Datalink. We employed a prevalent new-user cohort design by which patients initiating statins were each matched to 2 concurrent nonusers by the time-conditional propensity score (TCPS). Patients were followed until the occurrence of the composite end point of myocardial infarction, stroke, hospitalized heart failure or CVD mortality, all-cause mortality, and incident type 2 DM. The Cox proportional hazards model was used to estimate the hazard ratio (HR) of each outcome associated with as-treated statin use, with adjustment for TCPS deciles and imbalanced covariables.
Among 1,768 statin initiators and 3,528 nonusers, 63 versus 340 CVD (3.0 per 100 person-years versus 2.7 per 100 person-years) and 62 versus 525 deaths (2.8 per 100 person-years versus 4.1 per 100 person-years) occurred. Incident type 2 DM was noted in 128 of 3,608 statin initiators (3.0 per 100 person-years) and 518 of 7,208 nonusers (2.0 per 100 person-years). Statin initiation was associated with 32% (HR 0.68 [95% confidence interval (95% CI) 0.51-0.90]) reduction in CVD, 54% (HR 0.46 [95% CI 0.35-0.60]) reduction in all-cause mortality, and 33% increase in type 2 DM (HR 1.33 [95% CI 1.09-1.63]). The number needed to treat/number needed to harm to prevent a CVD or all-cause mortality or to cause type 2 DM in 1 year was 102, 42, and 127, respectively.
Statins are associated with important reductions in CVD and mortality that outweigh the modest increase in type 2 DM risk in RA patients.
评估使用他汀类药物对类风湿关节炎(RA)患者心血管疾病(CVD)风险、全因死亡率和2型糖尿病(DM)的影响。
我们在英国临床实践研究数据链中确定了一组1989年至2018年间的RA患者。我们采用了一种现患新使用者队列设计,即根据时间条件倾向评分(TCPS),将开始使用他汀类药物的患者与2名同时期未使用者进行匹配。对患者进行随访,直至出现心肌梗死、中风、住院心力衰竭或CVD死亡、全因死亡以及2型糖尿病发病的复合终点。使用Cox比例风险模型估计与实际使用他汀类药物相关的各结局的风险比(HR),并对TCPS十分位数和不均衡的协变量进行调整。
在1768名开始使用他汀类药物的患者和3528名未使用者中,分别发生了63例和340例CVD(每百人年3.0例对每百人年2.7例)以及62例和525例死亡(每百人年2.8例对每百人年4.1例)。在3608名开始使用他汀类药物的患者中有128例发生2型糖尿病(每百人年3.0例),在7208名未使用者中有518例发生(每百人年2.0例)。开始使用他汀类药物与CVD风险降低32%(HR 0.68 [95%置信区间(95%CI)0.51 - 0.90])、全因死亡率降低54%(HR 0.46 [95%CI 0.35 - 0.60])以及2型糖尿病风险增加33%(HR 1.33 [95%CI 1.09 - 1.63])相关。在1年内预防1例CVD或全因死亡或导致1例2型糖尿病所需治疗人数 / 造成伤害人数分别为102、42和127。
他汀类药物与RA患者CVD和死亡率的显著降低相关,这超过了2型糖尿病风险的适度增加。