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DOI 10.1056/nejmoa2607314

Медицинская библиотека · The New England journal of medicine · 2026

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

Zoungas Sophia, Wolfe Rory, Moran Chris, Nicholls Stephen J, Cloud Geoffrey C, Reid Christopher M, Τonkin Andrew M, Beilin Lawrence, Wierzbicki Anthony S, Chong Trevor T-J, Broder Jonathan C, Curtis Andrea J, Flanagan Zachary, Hopper Ingrid, Ryan Joanne, Spark Simone, McNeil John J, Nelson Mark R, STAREE Investigators

СтатьяРандомизированное исследованиеПеревод пока не подготовлен

Аннотация

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.).

Для цитирования: Zoungas Sophia, Wolfe Rory, Moran Chris, Nicholls Stephen J, Cloud Geoffrey C, Reid Christopher M, Τonkin Andrew M, Beilin Lawrence, Wierzbicki Anthony S, Chong Trevor T-J, Broder Jonathan C, Curtis Andrea J, Flanagan Zachary, Hopper Ingrid, Ryan Joanne, Spark Simone, McNeil John J, Nelson Mark R, STAREE Investigators. Atorvastatin, Cardiovascular Events, and Disability-free Survival in Older Adults.. The New England journal of medicine. 2026. DOI: 10.1056/nejmoa2607314.

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