Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia
Member Health, Medibank Private, Melbourne, Victoria, Australia.
BMJ Open. 2020 Feb 20;10(2):e026876. doi: 10.1136/bmjopen-2018-026876.
This review provides insights into the potential for aspirin to preserve bone mineral density (BMD) and reduce fracture risk, building knowledge of the risk-benefit profile of aspirin.
We conducted a systematic review and exploratory meta-analysis of observational studies. Electronic searches of MEDLINE and Embase, and a manual search of bibliographies was undertaken for studies published to 28 March 2018. Studies were included if: participants were men or women aged ≥18 years; the exposure of interest was aspirin; and relative risks, ORs and 95% CIs for the risk of fracture or difference (percentage or absolute) in BMD (measured by dual energy X-ray absorptiometry) between aspirin users and non-users were presented. Risk of bias was assessed using the Joanna Briggs Institute Critical Appraisal Checklists for observational studies. Pooled ORs for any fracture and standardised mean differences (SMDs) for BMD outcomes were calculated using random-effects models.
Twelve studies met the inclusion criteria and were included in the meta-analysis. Aspirin use was associated with a 17% lower odds for any fracture (OR 0.83, 95% CI 0.70 to 0.99; I=71%; six studies; n=511 390). Aspirin was associated with a higher total hip BMD for women (SMD 0.03, 95% CI -0.02 to 0.07; I=0%; three studies; n=9686) and men (SMD 0.06, 95% CI -0.02 to 0.13, I=0%; two studies; n=4137) although these associations were not significant. Similar results were observed for lumbar spine BMD in women (SMD 0.03, 95% CI -0.03 to 0.09; I=34%; four studies; n=11 330) and men (SMD 0.08; 95% CI -0.01 to 0.18; one study; n=432).
While the benefits of reduced fracture risk and higher BMD from aspirin use may be modest for individuals, if confirmed in prospective controlled trials, they may confer a large population benefit given the common use of aspirin in older people.
本综述旨在探讨阿司匹林对维持骨密度(BMD)和降低骨折风险的潜力,加深对阿司匹林风险-效益特征的认识。
我们对截至 2018 年 3 月 28 日发表的观察性研究进行了系统回顾和探索性荟萃分析。我们对 MEDLINE 和 Embase 进行了电子检索,并对参考文献进行了手工检索。如果研究符合以下标准,我们将其纳入分析:参与者为年龄≥18 岁的男性或女性;研究的暴露因素为阿司匹林;并报告了阿司匹林使用者和非使用者之间骨折风险或 BMD(双能 X 射线吸收法测定)差异(百分比或绝对差异)的相对风险(RR)、比值比(OR)和 95%置信区间(CI)。使用 Joanna Briggs 研究所的观察性研究批判性评价清单评估偏倚风险。使用随机效应模型计算任何骨折的汇总 OR 和 BMD 结局的标准化均数差值(SMD)。
共有 12 项研究符合纳入标准,并纳入荟萃分析。阿司匹林的使用与任何骨折的风险降低 17%相关(OR 0.83,95%CI 0.70 至 0.99;I=71%;6 项研究;n=511390)。阿司匹林与女性(SMD 0.03,95%CI -0.02 至 0.07;I=0%;3 项研究;n=9686)和男性(SMD 0.06,95%CI -0.02 至 0.13,I=0%;2 项研究;n=4137)的全髋骨密度升高相关,但这些关联无统计学意义。女性(SMD 0.03,95%CI -0.03 至 0.09;I=34%;4 项研究;n=11330)和男性(SMD 0.08;95%CI -0.01 至 0.18;1 项研究;n=432)的腰椎骨密度也有类似的结果。
虽然阿司匹林降低骨折风险和提高 BMD 的获益对个体而言可能较小,但如果在前瞻性对照试验中得到证实,鉴于老年人中阿司匹林的广泛使用,它们可能会带来较大的人群获益。