From the Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
A.M. Jorge, MD, Graduate Assistant, Research Fellow, Massachusetts General Hospital, and Harvard Medical School; N. Lu, MPH, Research Assistant, Massachusetts General Hospital; S.F. Keller, MD, Rheumatology Fellow, Research Fellow, Massachusetts General Hospital, and Harvard Medical School; S.K. Rai, MSc, Research Assistant, Massachusetts General Hospital; Y. Zhang, DSc, Faculty, Harvard Medical School; H.K. Choi, MD, PhD, Professor, Harvard Medical School.
J Rheumatol. 2018 Dec;45(12):1689-1695. doi: 10.3899/jrheum.171389. Epub 2018 Sep 1.
Systemic autoimmune rheumatic diseases (SARD) are associated with an increased risk of premature cardiovascular disease (CVD) and all-cause mortality. We examined the potential survival benefit of statin use among patients with SARD in a general population setting.
We conducted an incident user cohort study using a UK general population database. Our population included patients with a SARD as determined by Read code diagnoses of systemic lupus erythematosus, systemic sclerosis, Sjögren syndrome, dermatomyositis, polymyositis, mixed connective tissue disease, Behçet disease, or antineutrophil cytoplasmic antibodies-associated vasculitis between January 1, 2000, and December 31, 2014. We compared propensity score-matched cohorts of statin initiators and noninitiators within 1-year cohort accrual blocks to account for potential confounders, including disease duration, body mass index, lifestyle factors, comorbidities, and medication use.
Of 2305 statin initiators, 298 died during the followup period (mean 5.1 yrs), whereas among 2305 propensity score-matched noninitiators, 338 died during the followup period (mean 4.8 yrs). This corresponded to mortality rates of 25.4/1000 and 30.3/1000 person-years, respectively. Statin initiation was associated with reduced all-cause mortality (HR 0.84, 95% CI 0.72-0.98). When we compared the unmatched cohorts, the statin initiators (n = 2863) showed increased mortality (HR 1.85, 95% CI 1.58-2.16) compared with noninitiators (n = 2863 randomly selected within 1-year cohort accrual blocks) because of confounding by indication.
In this general population-based study, statin initiation was shown to reduce overall mortality in patients with SARD after adjusting for relevant determinates of CVD risk.
系统性自身免疫性风湿病(SARD)与过早发生心血管疾病(CVD)和全因死亡率增加相关。我们在一般人群中研究了 SARD 患者使用他汀类药物的潜在生存获益。
我们使用英国一般人群数据库进行了一项以患者为基础的队列研究。我们的研究人群包括 2000 年 1 月 1 日至 2014 年 12 月 31 日期间,根据 Read 诊断代码确定的患有系统性红斑狼疮、系统性硬化症、干燥综合征、皮肌炎、多发性肌炎、混合性结缔组织病、贝赫切特病或抗中性粒细胞胞浆抗体相关性血管炎的 SARD 患者。我们比较了在 1 年内的队列纳入期内,他汀类药物使用者和非使用者的倾向评分匹配队列,以考虑潜在的混杂因素,包括疾病持续时间、体重指数、生活方式因素、合并症和药物使用情况。
在 2305 名他汀类药物使用者中,有 298 人在随访期间死亡(平均随访时间为 5.1 年),而在 2305 名匹配的非他汀类药物使用者中,有 338 人在随访期间死亡(平均随访时间为 4.8 年)。相应的死亡率分别为 25.4/1000 和 30.3/1000 人年。他汀类药物的使用与全因死亡率降低相关(HR 0.84,95%CI 0.72-0.98)。当我们比较未匹配的队列时,他汀类药物使用者(n = 2863)的死亡率高于非使用者(n = 2863 人在 1 年内的队列纳入期内随机选择)(HR 1.85,95%CI 1.58-2.16),这是由于存在指向性混淆。
在这项基于一般人群的研究中,调整了 CVD 风险的相关决定因素后,SARD 患者开始使用他汀类药物可降低总体死亡率。