Veronese Nicola, Stubbs Brendon, Maggi Stefania, Thompson Trevor, Schofield Patricia, Muller Christoph, Tseng Ping-Tao, Lin Pao-Yen, Carvalho André F, Solmi Marco
Institute for Clinical Research and Education in Medicine, Padova, Italy.
Aging Section, Institute of Neurosciences, Italian Research Council, Padova, Italy.
J Am Geriatr Soc. 2017 Aug;65(8):1763-1768. doi: 10.1111/jgs.14883. Epub 2017 Apr 20.
To investigate whether low-dose aspirin (<300 mg/d) can influence the onset of cognitive impairment or dementia in observational studies and improve cognitive test scores in randomized controlled trials (RCTs) in participants without dementia.
Systematic review and meta-analysis.
Observational and interventional studies.
Individuals with no dementia or cognitive impairment initially.
Odds ratios (ORs) and 95% confidence intervals (CIs), adjusted for the maximum number of covariates from each study, were used to summarize data on the incidence of dementia and cognitive impairment in observational studies. Standardized mean differences (SMDs) were used for cognitive test scores in RCTs.
Of 2,341 potentially eligible articles, eight studies were included and provided data for 36,196 participants without dementia or cognitive impairment at baseline (mean age 66, 63% female). After adjusting for a median of three potential confounders over a median follow-up period of 6 years, chronic use of low-dose aspirin was not associated with onset of dementia or cognitive impairment (5 studies, N = 26,159; OR = 0.82, 95% CI = 0.55-1.22, P = .33, I = 67%). In three RCTs (N = 10,037; median follow-up 5 years), the use of low-dose aspirin was not associated with significantly better global cognition (SMD=0.005, 95% CI=-0.04-0.05, P = .84, I = 0%) in individuals without dementia. Adherence was lower in participants taking aspirin than in controls, and the incidence of adverse events was higher.
This review found no evidence that low-dose aspirin buffers against cognitive decline or dementia or improves cognitive test scores in RCTs.
在观察性研究中调查低剂量阿司匹林(<300毫克/天)是否会影响认知障碍或痴呆的发病,并在无痴呆参与者的随机对照试验(RCT)中提高认知测试分数。
系统评价和荟萃分析。
观察性和干预性研究。
最初无痴呆或认知障碍的个体。
在观察性研究中,使用根据每项研究的最大协变量数量进行调整的优势比(OR)和95%置信区间(CI)来汇总痴呆和认知障碍发病率的数据。在随机对照试验中,使用标准化均数差(SMD)来衡量认知测试分数。
在2341篇可能符合条件的文章中,纳入了8项研究,为36196名基线时无痴呆或认知障碍的参与者(平均年龄66岁,63%为女性)提供了数据。在中位随访期6年、对中位3个潜在混杂因素进行调整后,长期使用低剂量阿司匹林与痴呆或认知障碍的发病无关(5项研究,N = 26159;OR = 0.82,95%CI = 0.55 - 1.22,P = 0.33,I² = 67%)。在3项随机对照试验(N = 10037;中位随访5年)中,使用低剂量阿司匹林与无痴呆个体的整体认知改善无显著关联(SMD = 0.005,95%CI = -0.04 - 0.05,P = 0.84,I² = 0%)。服用阿司匹林的参与者依从性低于对照组,不良事件发生率更高。
本综述未发现证据表明低剂量阿司匹林可预防认知功能下降或痴呆,或在随机对照试验中提高认知测试分数。