학술논문

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Document Type
article
Author
Malik, RainerChauhan, GaneshTraylor, MatthewSargurupremraj, MuralidharanOkada, YukinoriMishra, AniketRutten-Jacobs, LoesGiese, Anne-Katrinvan der Laan, Sander WGretarsdottir, SolveigAnderson, Christopher DChong, MichaelAdams, Hieab HHAgo, TetsuroAlmgren, PeterAmouyel, PhilippeAy, HakanBartz, Traci MBenavente, Oscar RBevan, SteveBoncoraglio, Giorgio BBrown, Robert DButterworth, Adam SCarrera, CatyCarty, Cara LChasman, Daniel IChen, Wei-MinCole, John WCorrea, AdolfoCotlarciuc, IoanaCruchaga, CarlosDanesh, Johnde Bakker, Paul IWDeStefano, Anita Lden Hoed, MarcelDuan, QingEngelter, Stefan TFalcone, Guido JGottesman, Rebecca FGrewal, Raji PGudnason, VilmundurGustafsson, StefanHaessler, JeffreyHarris, Tamara BHassan, AhamadHavulinna, Aki SHeckbert, Susan RHolliday, Elizabeth GHoward, GeorgeHsu, Fang-ChiHyacinth, Hyacinth IIkram, M ArfanIngelsson, ErikIrvin, Marguerite RJian, XueqiuJiménez-Conde, JordiJohnson, Julie AJukema, J WouterKanai, MasahiroKeene, Keith LKissela, Brett MKleindorfer, Dawn OKooperberg, CharlesKubo, MichiakiLange, Leslie ALangefeld, Carl DLangenberg, ClaudiaLauner, Lenore JLee, Jin-MooLemmens, RobinLeys, DidierLewis, Cathryn MLin, Wei-YuLindgren, Arne GLorentzen, ErikMagnusson, Patrik KMaguire, JaneManichaikul, AniMcArdle, Patrick FMeschia, James FMitchell, Braxton DMosley, Thomas HNalls, Michael ANinomiya, ToshiharuO’Donnell, Martin JPsaty, Bruce MPulit, Sara LRannikmäe, KristiinaReiner, Alexander PRexrode, Kathryn MRice, KennethRich, Stephen SRidker, Paul MRost, Natalia SRothwell, Peter MRotter, Jerome IRundek, TatjanaSacco, Ralph LSakaue, SaoriSale, Michele M
Source
Nature Genetics. 50(4)
Subject
Biological Sciences
Genetics
Human Genome
Stroke
Clinical Research
Brain Disorders
Aetiology
2.1 Biological and endogenous factors
Cardiovascular
Computational Biology
Databases
Genetic
Epigenesis
Genetic
Female
Gene Regulatory Networks
Genetic Loci
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
INDEL Mutation
Linkage Disequilibrium
Male
Models
Genetic
Polymorphism
Single Nucleotide
Risk Factors
AFGen Consortium
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
International Genomics of Blood Pressure (iGEN-BP) Consortium
INVENT Consortium
STARNET
BioBank Japan Cooperative Hospital Group
COMPASS Consortium
EPIC-CVD Consortium
EPIC-InterAct Consortium
International Stroke Genetics Consortium
METASTROKE Consortium
Neurology Working Group of the CHARGE Consortium
NINDS Stroke Genetics Network
UK Young Lacunar DNA Study
MEGASTROKE Consortium
Medical and Health Sciences
Developmental Biology
Agricultural biotechnology
Bioinformatics and computational biology
Language
Abstract
Stroke has multiple etiologies, but the underlying genes and pathways are largely unknown. We conducted a multiancestry genome-wide-association meta-analysis in 521,612 individuals (67,162 cases and 454,450 controls) and discovered 22 new stroke risk loci, bringing the total to 32. We further found shared genetic variation with related vascular traits, including blood pressure, cardiac traits, and venous thromboembolism, at individual loci (n = 18), and using genetic risk scores and linkage-disequilibrium-score regression. Several loci exhibited distinct association and pleiotropy patterns for etiological stroke subtypes. Eleven new susceptibility loci indicate mechanisms not previously implicated in stroke pathophysiology, with prioritization of risk variants and genes accomplished through bioinformatics analyses using extensive functional datasets. Stroke risk loci were significantly enriched in drug targets for antithrombotic therapy.