Toyli Aili, Zhao Chen, Su Kuan-Jui, Shen Hui, Deng Hong-Wen, Chen Qing-Hui, Sha Qiuying, Zhou Weihua
Department of Mathematical Sciences, Michigan Technological University, Houghton, MI, USA 49931.
Department of Computer Science, Kennesaw State University, 680 Arntson Dr, Marietta, GA, USA 30060.
medRxiv. 2025 Sep 2:2025.08.29.25334750. doi: 10.1101/2025.08.29.25334750.
Cardiovascular disease (CVD) and Alzheimer's disease (AD) are major public health concerns that share overlapping risk factors and potential mechanistic pathways. While vascular contributions to cognitive decline are well-documented, the specific relationships between AD and different CVD subtypes remain poorly understood.
We examined associations between AD and 11 CVD subtypes using logistic regression models in two large biobanks: the UK Biobank (n = 502,133) and the All of Us Research Program (n = 287,011). Models were adjusted for demographic, lifestyle, and clinical covariates. We also explored genetic overlap between AD and CVD traits through colocalization of significant single nucleotide polymorphisms (SNPs) (p < 5×10) using genome-wide association study (GWAS) data.
Most CVD subtypes were significantly associated with AD in both cohorts. Hypotension had the strongest and most consistent association, followed by hypertension and cerebral infarction. Acute myocardial infarction was the only subtype not significantly linked to AD. Genetic analyses revealed shared loci between AD and CVD-related traits, particularly in regions near , and genes influencing myocardial structure and vascular function.
This study identifies subtype-specific CVD associations with AD across two diverse cohorts and highlights shared genetic architecture underlying heart-brain interactions. These findings underscore the importance of vascular health in AD risk and suggest that certain CVD subtypes, especially hypotension, may play underrecognized roles in cognitive decline.
心血管疾病(CVD)和阿尔茨海默病(AD)是主要的公共卫生问题,它们具有重叠的风险因素和潜在的机制途径。虽然血管对认知衰退的影响已有充分记录,但AD与不同CVD亚型之间的具体关系仍知之甚少。
我们在两个大型生物样本库中使用逻辑回归模型研究了AD与11种CVD亚型之间的关联:英国生物样本库(n = 502,133)和“我们所有人”研究计划(n = 287,011)。模型对人口统计学、生活方式和临床协变量进行了调整。我们还通过使用全基因组关联研究(GWAS)数据对显著单核苷酸多态性(SNP)(p < 5×10)进行共定位,探索了AD与CVD特征之间的遗传重叠。
在两个队列中,大多数CVD亚型都与AD显著相关。低血压的关联最强且最一致,其次是高血压和脑梗死。急性心肌梗死是唯一与AD无显著关联的亚型。遗传分析揭示了AD与CVD相关特征之间的共享基因座,特别是在 附近的区域,以及影响心肌结构和血管功能的基因。
本研究在两个不同队列中确定了CVD亚型与AD的特异性关联,并突出了心脑相互作用背后共享的遗传结构。这些发现强调了血管健康在AD风险中的重要性,并表明某些CVD亚型,尤其是低血压,可能在认知衰退中发挥未被充分认识的作用。