Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, People's Republic of China.
Department of Pharmacology, Physiology, and Biophysics, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Ann Neurol. 2024 Dec;96(6):1124-1134. doi: 10.1002/ana.27108. Epub 2024 Oct 15.
Sex differences in the association between cardiovascular risk factors and the incident all-cause dementia and the subtype Alzheimer's disease (AD) risk are unclear.
Framingham Heart Study (FHS) participants (n = 4,171, 54% women, aged 55 to 69 years) were included at baseline and followed up to 40 years. The Framingham Stroke Risk Profile (FSRP) was dichotomized into 2 levels (cutoff: 75th percentile of the FSRP z-scores). Cause-specific hazard models, with death as a competing event, and restricted mean survival time (RMST) model were used to analyze the association between FSRP levels and incident all-cause dementia and AD. Interactions between FSRP and sex were estimated, followed by a sex-stratified analysis to examine the sex modification effect.
High FSRP was significantly associated with all-cause dementia (hazard ratio [HR] = 1.25, robust 95% confidence interval [CI] = 1.21 to 1.29, p < 0.001) and AD (HR = 1.58, robust 95% CI = 1.57 to 1.59, p < 0.001) in cause-specific hazard models. High FSRP was significantly associated with incident dementia (HR = 2.81, robust 95% CI = 2.75 to 2.87, p < 0.001) and AD (HR = 2.96, robust 95% CI = 2.36 to 3.71, p < 0.001) in women, but not in men. Results were consistent in the RMST models. Current diabetes and high systolic blood pressure as FSRP components were significantly associated with dementia and AD in women but not in men.
High FSRP in mid- to early late life is a critical risk factor for all-cause dementia and AD, particularly in women. Sex-specific interventions and further research to elucidate underlying mechanisms are warranted. ANN NEUROL 2024;96:1124-1134.
心血管危险因素与全因痴呆和阿尔茨海默病(AD)发病风险之间的性别差异尚不清楚。
纳入弗雷明汉心脏研究(FHS)参与者(n=4171,54%为女性,年龄 55 至 69 岁),在基线时进行入组并随访 40 年。将弗雷明汉卒中风险评分(FSRP)分为 2 个水平(截断值:FSRPz 分数的 75 百分位数)。使用具有死亡作为竞争事件的特定病因风险模型和限制性平均生存时间(RMST)模型,分析 FSRP 水平与全因痴呆和 AD 发病的相关性。估计 FSRP 与性别之间的交互作用,然后进行性别分层分析,以检验性别修饰作用。
高 FSRP 与全因痴呆(风险比[HR] = 1.25,稳健 95%置信区间[CI] = 1.21 至 1.29,p<0.001)和 AD(HR = 1.58,稳健 95%CI = 1.57 至 1.59,p<0.001)显著相关。在特定病因风险模型中,高 FSRP 与痴呆发病(HR = 2.81,稳健 95%CI = 2.75 至 2.87,p<0.001)和 AD(HR = 2.96,稳健 95%CI = 2.36 至 3.71,p<0.001)显著相关。在女性中,而不是在男性中,高 FSRP 与 AD 显著相关。RMST 模型的结果一致。作为 FSRP 组成部分的当前糖尿病和高收缩压与女性的痴呆和 AD 显著相关,但与男性无关。
中年至早期晚年的高 FSRP 是全因痴呆和 AD 的重要危险因素,尤其是在女性中。需要针对女性进行特定性别干预和进一步研究,以阐明潜在机制。