Open AccessWhole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
Author(s) -
Raghavan Neha S.,
Brickman Adam M.,
Andrews Howard,
Manly Jennifer J.,
Schupf Nicole,
Lantigua Rafael,
Wolock Charles J.,
Kamalakaran Sitharthan,
Petrovski Slave,
Tosto Giuseppe,
Vardarajan Badri N.,
Goldstein David B.,
Mayeux Richard
Publication year - 2018
Publication title -
annals of clinical and translational neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.824
H-Index - 42
ISSN - 2328-9503
DOI - 10.1002/acn3.582
Subject(s) - exome sequencing , loss function , medicine , disease , exome , alzheimer's disease , alzheimer's disease neuroimaging initiative , genetics , case control study , gene , bioinformatics , biology , phenotype
Objective The genetic bases of Alzheimer's disease remain uncertain. An international effort to fully articulate genetic risks and protective factors is underway with the hope of identifying potential therapeutic targets and preventive strategies. The goal here was to identify and characterize the frequency and impact of rare and ultra‐rare variants in Alzheimer's disease, using whole‐exome sequencing in 20,197 individuals. Methods We used a gene‐based collapsing analysis of loss‐of‐function ultra‐rare variants in a case–control study design with data from the Washington Heights‐Inwood Columbia Aging Project, the Alzheimer's Disease Sequencing Project and unrelated individuals from the Institute of Genomic Medicine at Columbia University. Results We identified 19 cases carrying extremely rare SORL 1 loss‐of‐function variants among a collection of 6,965 cases and a single loss‐of‐function variant among 13,252 controls ( P = 2.17 × 10 −8 ; OR : 36.2 [95% CI : 5.8–1493.0]). Age‐at‐onset was 7 years earlier for patients with SORL 1 qualifying variant compared with noncarriers. No other gene attained a study‐wide level of statistical significance, but multiple top‐ranked genes, including GRID 2 IP , WDR 76 and GRN , were among candidates for follow‐up studies. Interpretation This study implicates ultra‐rare, loss‐of‐function variants in SORL 1 as a significant genetic risk factor for Alzheimer's disease and provides a comprehensive dataset comparing the burden of rare variation in nearly all human genes in Alzheimer's disease cases and controls. This is the first investigation to establish a genome‐wide statistically significant association between multiple extremely rare loss‐of‐function variants in SORL 1 and Alzheimer's disease in a large whole‐exome study of unrelated cases and controls.