Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole‐genome sequencing from the Alzheimer's Disease Sequencing Project
Wan‐Ping Lee, Seung Hoan Choi, Margaret G. Shea, Po‐Liang Cheng, Beth A. Dombroski, Achilleas Pitsillides, Nancy L. Heard‐Costa, Hui Wang, Katia Bulekova, Amanda B Kuzma, Yuk Yee Leung, John J. Farrell, Honghuang Lin, Brian W. Kunkle, Adam C. Naj, Elizabeth Blue, Frederick Nusetor, Dongyu Wang, Eric Boerwinkle, William S. Bush, Xiaoling Zhang, Philip L. De Jager, Josée Dupuis, Lindsay A. Farrer, Myriam Fornage, Eden R. Martin, Margaret Pericak‐Vance, Sudha Seshadri, Ellen M. Wijsman, Li‐San Wang, The Alzheimer's Disease Sequencing Project, Gerard D. Schellenberg, Anita L. DeStefano, Jonathan L. Haines, Gina M. Peloso
Abstract
Abstract INTRODUCTION Alzheimer's disease (AD) is a common disorder of the elderly that is both highly heritable and genetically heterogeneous. METHODS We investigated the association of AD with both common variants and aggregates of rare coding and non‐coding variants in 13,371 individuals of diverse ancestry with whole genome sequencing (WGS) data. RESULTS Pooled‐population analyses of all individuals identified genetic variants at apolipoprotein E ( APOE ) and BIN1 associated with AD ( p < 5 × 10 −8 ). Subgroup‐specific analyses identified a haplotype on chromosome 14 including PSEN1 associated with AD in Hispanics, further supported by aggregate testing of rare coding and non‐coding variants in the region. Common variants in LINC00320 were observed associated with AD in Black individuals ( p = 1.9 × 10 −9 ). Finally, we observed rare non‐coding variants in the promoter of TOMM40 distinct of APOE in pooled‐population analyses ( p = 7.2 × 10 −8 ). DISCUSSION We observed that complementary pooled‐population and subgroup‐specific analyses offered unique insights into the genetic architecture of AD. Highlights We determine the association of genetic variants with Alzheimer's disease (AD) using 13,371 individuals of diverse ancestry with whole genome sequencing (WGS) data. We identified genetic variants at apolipoprotein E ( APOE ), BIN1 , PSEN1 , and LINC00320 associated with AD. We observed rare non‐coding variants in the promoter of TOMM40 distinct of APOE .