时间标签:数据日期 2026-10-31 · 生成时间 2026-11-01 05:30(Asia/Shanghai)| 检索窗口 PubMed edat 2026/10/28–2026/10/31 | 情报发生日期 2026-10-31
研究问题
Bischoff‑Ferrari Received: 8 August 2026 / Accepted: 22 October 2026 © The Author(s) 2026 Abstract Chronic low-grade inflammation (“inflam- maging”) drives age-related decline, but whether anti- inflammatory medications preserve functional per- formance in older age remains unknown.;However, the risk–benefit of aspirin for primary prevention in older adults remained unclear.;However, the data available from the trial enabled annual assessment of four of the five IC domains, according to the WHO Framework (as sum- marised below).
方法
Vol.: (0123456789) GeroScience https://doi.org/10.1007/s11357-026-02624-x ORIGINAL ARTICLE Validation of an intrinsic capacity index and the effects of aspirin in older males and females: secondary analysis of a randomized controlled trial Joanne Ryan · Aung Zaw Zaw Phyo · Maud Wieczorek · Sara Espinoza · Robyn L.;A post-hoc analysis of a randomised controlled trial com- paring daily 100 mg aspirin to placebo in prolonging dementia- and disability-free survival (DFS) in commu- nity-dwelling individuals aged≥65 years.;A four-domain IC score (including cognition, locomotion, vitality and psychological well-being) was calculated annually across 18,581 participants and validated against biologi- cal and clinical measures.;Females randomized to aspirin had a small but significantly accelerated decline in IC (β:−0.006, 95% CI:−0.01,−0.001, p=0.01), whereas no effect was observed in males (p=0.
核心结论
Females had lower baseline IC and a steeper decline over time than males.;Clinically, lower baseline IC was associated with reduced DFS in both sexes (Q1 vs.;Q5: HR=4.62, 95% CI: 3.16–6.75; HR=4.32, 95% CI: 3.42–5.48). ‖ 结论:Ultimately, these findings highlight the critical need for sex-stratified analyses in geroscience trials and suggest that future interventions targeting age-related inflammation must be precision-guided to safely and effectively maintain healthy aging.
局限
Par- ticipants self-reported their sex and race (nine options, including more than one race) and ethnic- ity (Hispanic/Latino or not).;Approximately 90% of Australian participants completed questionnaires that included self-reported hearing and eyesight.;The sensory domain was calculated by averaging the z-scores of self-reported vision and hearing. i) Eyesight: At both time-points, participants rated their eyesight on a 6-point Likert scale as excellent to very poor, or completely blind.
对本项目的价值
★★★☆☆ 干预证据决定参照标准效应量——任何抗衰干预的收益至少应对标该基线。设计 randomised controlled trial;最大样本量约 18,581。
全文来源
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原文题录
- 英文标题:Validation of an intrinsic capacity index and the effects of aspirin in older males and females: secondary analysis of a randomized controlled trial.
- 期刊与标识:Geroscience · PMID 42955660 · DOI 10.1007/s11357-026-02624-x
A 级证据分级:A 级(同行评议人体研究)
本文属人体研究证据,但需注意:观察性或小样本干预的结论不等于已证实临床获益;效应量与长期安全性仍需更大规模、更长随访的试验验证。
关于本文的文献来源:本站依据 IMA 知识库「五刊监控·深度文献卡片」撰写,依据已获取的期刊全文(方法、样本量与结论已回到原文核对);未能获取全文的同批条目另行标注「摘要级」,全程未做任何数值推算补全。