Xu Yuexuan, Sun Zhongxuan, Jonaitis Erin, Deming Yuetiva, Lu Qiongshi, Johnson Sterling C, Engelman Corinne D
G.H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Columbia University.
Department of Biostatistics and Medical Informatics, School of Medicine and Public Health, University of Wisconsin-Madison.
medRxiv. 2024 May 27:2024.05.26.24307953. doi: 10.1101/2024.05.26.24307953.
Genetic and lifestyle factors contribute to an individual's risk of developing Alzheimer's disease. However, it is unknown whether and how adherence to healthy lifestyles can mitigate the genetic risk of Alzheimer's.
The aim of this study is to investigate whether adherence to healthy lifestyles can modify the impact of genetic predisposition to Alzheimer's disease on later-life cognitive decline.
This prospective cohort study included 891 adults of European ancestry, aged 40 to 65, who were without dementia and had complete healthy-lifestyle and cognition data during the follow-up. Participants joined the Wisconsin Registry for Alzheimer's Prevention (WRAP) beginning in 2001. We conducted replication analyses using a subsample with similar baseline age range from the Health and Retirement Study (HRS).
We assessed participants' exposures using a continuous non- polygenic risk score for Alzheimer's, a binary indicator for carrier status, and a weighted healthy-lifestyle score, including factors such as no current smoking, regular physical activity, healthy diet, light to moderate alcohol consumption, and frequent cognitive activities.
We z-standardized cognitive scores for global (Preclinical Alzheimer's Cognitive Composite score 3 - PACC3) and domain-specific assessments (delayed recall and immediate learning).
We followed 891 individuals for up to 10 years (mean [SD] baseline age, 58 [6] years, 31% male, 38% carriers). After false discovery rate (FDR) correction, we found statistically significant PRS × lifestyle × age interactions on preclinical cognitive decline but the evidence is stronger among carriers. Among carriers, PRS-related differences in overall and memory-related domains between people scoring 0-1 and 4-5 regarding healthy lifestyles became evident around age 67 after FDR correction. These findings were robust across several sensitivity analyses and were replicated in the population-based HRS.
A favorable lifestyle can mitigate the genetic risk associated with current known non- genetic variants for longitudinal cognitive decline, and these protective effects are particularly pronounced among carriers.
遗传和生活方式因素会影响个体患阿尔茨海默病的风险。然而,坚持健康的生活方式是否以及如何能减轻阿尔茨海默病的遗传风险尚不清楚。
本研究旨在调查坚持健康的生活方式是否能改变阿尔茨海默病遗传易感性对晚年认知衰退的影响。
设计、地点和参与者:这项前瞻性队列研究纳入了891名欧洲血统的成年人,年龄在40至65岁之间,无痴呆症,且在随访期间有完整的健康生活方式和认知数据。参与者于2001年开始加入威斯康星州阿尔茨海默病预防登记处(WRAP)。我们使用来自健康与退休研究(HRS)的具有相似基线年龄范围的子样本进行了重复分析。
我们使用阿尔茨海默病的连续非多基因风险评分、携带者状态的二元指标以及加权健康生活方式评分来评估参与者的暴露因素,加权健康生活方式评分包括当前不吸烟、定期体育活动、健康饮食、轻度至中度饮酒以及频繁进行认知活动等因素。
我们对整体(临床前阿尔茨海默病认知综合评分3 - PACC3)和特定领域评估(延迟回忆和即时学习)的认知评分进行了z标准化。
我们对891名个体进行了长达10年的随访(平均[标准差]基线年龄为58[6]岁,31%为男性,38%为携带者)。经过错误发现率(FDR)校正后,我们发现临床前认知衰退存在统计学上显著的多基因风险评分×生活方式×年龄相互作用,但在携带者中证据更强。在携带者中,经过FDR校正后,在67岁左右,健康生活方式评分为0 - 1分和4 - 5分的人群在整体和记忆相关领域中与多基因风险评分相关的差异变得明显。这些发现在多项敏感性分析中都很稳健,并在基于人群的HRS中得到了重复。
良好的生活方式可以减轻与当前已知非遗传变异相关的纵向认知衰退的遗传风险,并且这些保护作用在携带者中尤为明显。