Polygenic and polysocial risk scores in post-type 2 diabetes dementia: Risk stratification and predictive modeling in the UK Biobank cohort

生命银行 多基因风险评分 痴呆 队列 医学 队列研究 前瞻性队列研究 老年学 人口学 风险评估 遗传倾向 比例危险模型 糖尿病 基因-环境相互作用 心理学 2型糖尿病 社会环境 临床心理学 基因检测 社会支持 健康与退休研究 遗传关联
作者
Nan He,Hongmei Wu,Nan An,Jin Bu,Yiran Li,Yaqi Dai,Yanqiu Ou,Feiying He
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
卷期号:: 13872877261435200-13872877261435200
标识
DOI:10.1177/13872877261435200
摘要

BackgroundDementia is a common complication of type 2 diabetes mellitus (T2DM), influenced by both genetic susceptibility and social disadvantages. While polygenic risk scores (PRS) have been widely applied to assess genetic vulnerability, the contribution of social determinants and their interaction with genetic risk are less understood.ObjectiveThis study aimed to investigate the independent and joint effects of PRS and polysocial risk scores (PsRS) on post-T2DM dementia risk.MethodsA prospective cohort study was conducted using UK Biobank data. PsRS and PRS were derived from multidimensional social and genetic indicators, respectively. Cox proportional hazards models were used to examine their associations with dementia outcomes. In genetically susceptible individuals, seven machine learning models were applied to predict dementia risk. SHAP and ALE were used to interpret feature importance.ResultsAmong 5,624 participants with T2DM, those in the highest PsRS group had a markedly elevated risk of all-cause dementia (HR = 2.738; 95% CI: 1.556-4.818, p < 0.001). This association persisted among genetically susceptible individuals. Machine learning analyses in the medium-to-high PRS group showed that eXtreme Gradient Boosting (XGBoost) achieved the best predictive performance (F1 = 0.735, AUC = 0.726). SHAP interpretation highlighted employment status (mean |SHAP value| = 0.45) and educational level (mean |SHAP value| = 0.19) as the strongest social contributors to dementia risk.ConclusionsBoth social disadvantages and genetic susceptibility contribute to dementia risk in individuals with T2DM. These findings underscore the importance of addressing modifiable social factors in targeted dementia prevention strategies for high-genetic-risk populations.
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