Extended genome-wide association study employing the African Genome Resources Panel identifies novel susceptibility loci for Alzheimer’s Disease in individuals of African ancestry

Author:

Ray Nicholas R.,Kunkle Brian W.,Hamilton-Nelson Kara,Kurup Jiji T.,Rajabli Farid,Cosacak Mehmet I.,Kizil CaghanORCID,Jean-Francois Melissa,Cuccaro Michael,Reyes-Dumeyer Dolly,Cantwell Laura,Kuzma Amanda,Vance Jeffery M.,Gao Sujuan,Hendrie Hugh C.,Baiyewu Olusegun,Ogunniyi Adesola,Akinyemi Rufus O.,Lee Wan-Ping,Martin Eden R.,Wang Li-San,Beecham Gary W.ORCID,Bush William S.ORCID,Farrer Lindsay A.,Haines Jonathan L.,Byrd Goldie S.,Schellenberg Gerard D.,Mayeux RichardORCID,Pericak-Vance Margaret A.,Reitz Christiane,

Abstract

ABSTRACTINTRODUCTIONDespite a two-fold increased risk, individuals of African ancestry have been significantly underrepresented in Alzheimer’s Disease (AD) genomics efforts.METHODSGWAS of 2,903 AD cases and 6,265 cognitive controls of African ancestry. Within-dataset results were meta-analyzed, followed by gene-based and pathway analyses, and analysis of RNAseq and whole-genome sequencing data.RESULTSA novel AD risk locus was identified inMPDZon chromosome 9p23 (rs141610415, MAF=.002,P=3.68×10−9). Two additional novel common and nine novel rare loci approached genome-wide significance atP<9×10−7. Comparison of association and LD patterns between datasets with higher and lower degrees of African ancestry showed differential association patterns at chr12q23.2 (ASCL1), suggesting that the association is modulated by regional origin of local African ancestry.DISCUSSIONIncreased sample sizes and sample sets from Africa covering as much African genetic diversity as possible will be critical to identify additional disease-associated loci and improve deconvolution of local genetic ancestry effects.

Publisher

Cold Spring Harbor Laboratory

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