Alzheimer's disease genetic risk variants beyond APOE ε4 predict mortality. Issue 1 (14th August 2017)

• Record Type: Journal Article
• Authors: Mez, Jesse; Marden, Jessica R.; Mukherjee, Shubhabrata; Walter, Stefan; Gibbons, Laura E.; Gross, Alden L.; Zahodne, Laura B.; Gilsanz, Paola; Brewster, Paul; Nho, Kwangsik; Crane, Paul K.; Larson, Eric B.; Glymour, M. Maria
• Is Part Of: Alzheimer's & dementia. Volume 8:Issue 1(2017)
• Page Start: 188
• Page End: 195
• Publication Date: 2017-08-14
• Subjects: Alzheimer's disease -- Longevity -- Mortality -- Survival analysis -- Genetic risk score -- Selection bias -- Collider stratification bias -- Survivor bias -- Genome‐wide association study (GWAS) -- APOE -- Adult Changes in Thought (ACT) -- Health and Retirement Study (HRS) -- Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE); Alzheimer's disease -- Periodicals; Alzheimer's disease -- Diagnosis -- Periodicals; Dementia -- Periodicals; Dementia -- Diagnosis -- Periodicals; 616.831
• DOI: 10.1016/j.dadm.2017.07.002
• Languages: English
• ISSNs: 2352-8729

Abstract

Abstract: Introduction: We hypothesized that, like apolipoprotein E ( APOE ), other late‐onset Alzheimer's disease (LOAD) genetic susceptibility loci predict mortality. Methods: We used a weighted genetic risk score (GRS) from 21 non‐ APOE LOAD risk variants to predict survival in the Adult Changes in Thought and the Health and Retirement Studies. We meta‐analyzed hazard ratios and examined models adjusted for cognitive performance or limited to participants with dementia. For replication, we assessed the GRS‐longevity association in the Cohorts for Heart and Aging Research in Genomic Epidemiology, comparing cases surviving to age ≥90 years with controls who died between ages 55 and 80 years. Results: Higher GRS predicted mortality (hazard ratio = 1.05; 95% confidence interval: 1.00–1.10, P = .04). After adjusting for cognitive performance or restricting to participants with dementia, the relationship was attenuated and no longer significant. In case‐control analysis, the GRS was associated with reduced longevity (odds ratio = 0.64; 95% confidence interval: 0.41–1.00, P = .05). Discussion: Non‐ APOE LOAD susceptibility loci confer risk for mortality, likely through effects on dementia incidence. Highlights: A genetic risk score from 21 non‐ APOE late‐onset Alzheimer's disease risk variants predicts mortality. The genetic risk score likely confers risk for mortality through its effect on dementia incidence. Late‐onset Alzheimer's disease risk loci effect estimates from genome‐wide association unlikely suffer from selection bias.