Sex differences in genetic liability to modifiable Alzheimer's disease risk factors

Abstract

INTRODUCTIONAlzheimers disease (AD) shows sex differences in risk, clinical progression, and biomarker profiles, but whether inherited genetic liability to modifiable risk factors contributes differently to AD susceptibility in females and males remains unclear. We evaluated whether genetic relationships between several modifiable dementia risk factors and AD differ between females and males. METHODSWe integrated polygenic risk scores (PRSs) for modifiable risk factors, genome-wide genetic correlation, and two-sample Mendelian randomization (MR) analyses. PRS associations with AD diagnosis were evaluated in the Alzheimers Disease Genetics Consortium (n=27,751) and with AD plasma biomarkers in the Health and Aging Brain Study-Health Disparities (n=2,307-2,737, depending on the biomarker). Primary analyses evaluated female- and male-specific associations and compared sex-specific estimates. RESULTSEducational attainment and physical activity PRSs were associated with AD in both sexes. PRS sex differences were nominal for educational attainment, total cholesterol, and LDL cholesterol, but none remained significant after FDR correction. Genetic correlation showed FDR-significant sex differences for social isolation, physical activity, LDL cholesterol, and pulse pressure. MR identified FDR-significant associations within sex strata; higher HDL cholesterol was associated with lower AD risk in females, whereas higher total cholesterol and type 2 diabetes were associated with lower and higher AD risk, respectively, in males. Sensitivity analyses provided inconsistent support, and no sex difference in MR estimates remained significant after FDR correction. In HABS-HD, type 2 diabetes PRS was associated with higher NfL, BMI PRS with higher pTau181, and the composite PRS with higher NfL among males after FDR correction. DISCUSSIONEvidence that modifiable dementia risk factors relate differently to AD by sex was limited and depended on the genetic measure examined. Sex differences in genome-wide genetic overlap were not consistently reflected in PRS or MR, indicating that shared genetic architecture does not necessarily translate into sex-specific inherited liability or causal effects RESEARCH IN CONTEXTO_ST_ABSSystematic reviewC_ST_ABSWe reviewed the published literature on modifiable dementia risk factors, Alzheimers disease (AD) genetics, and sex differences using PubMed and relevant reference lists. Previous studies support genetic relationships between several modifiable risk factors and AD, but systematic comparisons of female- and male-specific relationships across complementary genetic approaches remain limited. InterpretatioThe strongest evidence of sex heterogeneity for modifiable risk factors and AD was observed in their shared genetic architectures, with FDR-significant female-male differences for social isolation, physical activity, LDL cholesterol, and pulse pressure. PRS and Mendelian randomization analyses provided less evidence of formal sex heterogeneity, suggesting that sex differences in shared genetic architecture do not necessarily imply sex-specific causal effects. Future directionsLarger sex-stratified and ancestry-diverse GWAS integrated with longitudinal exposure and biomarker data are needed to determine whether these signals reflect sex-dependent biological mechanisms and whether they have implications for dementia prevention. Highlights- Sex differences in AD-related genetic architecture were concentrated in behavioral, lipid, and vascular traits. - Genetic correlations with AD differed between females and males for social isolation, physical activity, LDL cholesterol, and pulse pressure. - PRS analyses implicated educational attainment and physical activity in AD in both sexes, but no PRS sex difference survived FDR correction. - MR identified associations within sex strata but provided little robust evidence of sex-specific causal effects.