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炎症、虚弱与阿司匹林使用:医师健康研究初步研究

Inflammation, Frailty, and Aspirin Use in the Physicians' Health Study: A Pilot Study.

机构信息

Ariela Orkaby, MD MPH, New England GRECC, 150 South Huntington, Boston, MA 02130, 857-364-3646,

出版信息

J Frailty Aging. 2024;13(4):582-585. doi: 10.14283/jfa.2024.37.

Abstract

Whether anti-inflammatory medications such as aspirin can lower the risk of frailty is an active area of investigation. In previous studies, we reported that regular aspirin use started in midlife was associated with a lower risk of frailty at older age. We therefore sought to further examine the relationship between inflammatory biomarkers, frailty and aspirin use in a pilot nested case-control study of 300 participants aged ≥60 years with available data to calculate a frailty index from the Physicians' Health Study, a completed randomized trial of aspirin that began in 1982. We selected 150 individuals who were frail (frailty index >0.2) and 150 who were not frail (frailty index <0.1). We then matched 29 low users of aspirin (≤60 days/year) 3:1 to 87 regular users of aspirin (>60 days/year). After matching on age, smoking status, history of diabetes and CVD, there was no significant association between aspirin use and level of frailty among those with elevated inflammatory biomarkers (all p>0.05). In this pilot study we did not find evidence of a mediation effect of CRP, TNFR-2 or IL-6 on the association between aspirin and frailty. Additional work is needed to elucidate the potential mechanistic pathways through which medications such as aspirin may be linked with frailty.

摘要

抗炎药物(如阿司匹林)是否可以降低衰弱的风险是一个活跃的研究领域。在之前的研究中,我们报告称,从中年开始定期使用阿司匹林与老年时衰弱的风险较低有关。因此,我们试图在一项纳入 300 名年龄≥60 岁的参与者的试点嵌套病例对照研究中进一步研究炎症生物标志物、衰弱和阿司匹林使用之间的关系,这些参与者有可用数据来计算从医师健康研究中计算出的衰弱指数,这是一项始于 1982 年的阿司匹林随机对照试验。我们选择了 150 名衰弱(衰弱指数>0.2)和 150 名不衰弱(衰弱指数<0.1)的个体。然后,我们将 29 名低剂量阿司匹林使用者(每年≤60 天)与 87 名常规剂量阿司匹林使用者(每年>60 天)按 3:1 进行匹配。在匹配年龄、吸烟状况、糖尿病和 CVD 病史后,在炎症生物标志物升高的人群中,阿司匹林使用与衰弱程度之间没有显著关联(所有 p>0.05)。在这项试点研究中,我们没有发现 CRP、TNFR-2 或 IL-6 对阿司匹林与衰弱之间关联的中介效应的证据。需要进一步的工作来阐明阿司匹林等药物与衰弱之间可能存在的潜在机制途径。

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