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Atorvastatin, Cardiovascular Events, and Disability-free Survival in Older Adults

医学 阿托伐他汀 心肌梗塞 安慰剂 置信区间 物理疗法 随机对照试验 内科学 临床终点 危险系数 血运重建 死因 心血管事件 比例危险模型 临床试验 意向治疗分析 队列研究 年轻人 生存分析 老年病科 前瞻性队列研究 痴呆 老年学
作者
Sophia Zoungas,Rory S Wolfe,Chris Moran,Stephen James Nicholls,Geoffrey C. CLOUD,Christopher Michael Reid,Andrew M. Τonkin,Lawrence Beilin,Anthony S. Wierzbicki,Trevor T.-J. Chong,Jonathan C. Broder,Andrea J. Curtis,Zachary Flanagan,Ingrid Hopper,Joanne L. Ryan,Simone Spark,John J. McNeil,Mark Raymond Nelson
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:395 (13): 1259-1272 被引量:7
标识
DOI:10.1056/nejmoa2607314
摘要

BACKGROUND: The effectiveness and safety of statins for the primary prevention of cardiovascular events and the extension of disability-free survival among older adults remain uncertain. METHODS: We conducted a double-blind, randomized, placebo-controlled trial at general medical practices across Australia. Community-dwelling adults at least 70 years of age with no history of cardiovascular disease, diabetes, or dementia were randomly assigned in a 1:1 ratio to receive atorvastatin at a dose of 40 mg once daily or identical placebo. The two primary end points were a composite of death from cardiovascular causes, nonfatal myocardial infarction or stroke, or coronary revascularization (to assess effects on major cardiovascular events) and a composite of death from any cause, dementia, or persistent physical disability (to assess effects on disability-free survival). Analyses were performed according to a hierarchical testing plan. RESULTS: A total of 9971 participants were enrolled: 4984 were assigned to receive atorvastatin and 4987 to receive placebo. The mean (±SD) age of the participants was 74.7±4.5 years, and 51.9% were women. After a median of 5.9 years, a primary cardiovascular event had occurred in 297 participants (10.9 events per 1000 person-years) in the atorvastatin group and in 412 participants (15.5 events per 1000 person-years) in the placebo group (hazard ratio, 0.70; 95% confidence interval [CI], 0.61 to 0.82; P<0.001). Death from any cause, dementia, or persistent physical disability occurred in 637 participants (21.6 events per 1000 person-years) in the atorvastatin group and in 676 participants (23.0 events per 1000 person-years) in the placebo group (hazard ratio, 0.94; 95% CI, 0.84 to 1.05; P = 0.25). Serious adverse events occurred in 131 participants (2.7%) in the atorvastatin group and in 129 (2.7%) in the placebo group, with musculoskeletal, hepatobiliary, and diabetes-related adverse events occurring more commonly in the atorvastatin group. CONCLUSIONS: Treatment with atorvastatin led to a lower risk of major cardiovascular events than placebo at a median of 5.9 years but did not result in longer disability-free survival among community-dwelling older adults without clinical cardiovascular disease. (Funded by the National Health and Medical Research Council and others; STAREE ClinicalTrials.gov number, NCT02099123.).
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