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Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease.

TitleGene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease.
Publication TypeJournal Article
Year of Publication2019
AuthorsBaker E, Sims R, Leonenko G, Frizzati A, Harwood JC, Grozeva D, Morgan K, Passmore P, Holmes C, Powell J, Brayne C, Gill M, Mead S, Bossù P, Spalletta G, Goate AM, Cruchaga C, Maier W, Heun R, Jessen F, Peters O, Dichgans M, FröLich L, Ramirez A, Jones L, Hardy J, Ivanov D, Hill M, Holmans P, Allen ND, B Morgan P, Seshadri S, Schellenberg GD, Amouyel P, Williams J, Escott-Price V
Corporate AuthorsGERAD/PERADES, CHARGE, ADGC, EADI, IGAP consortia
JournalPLoS One
Volume14
Issue7
Paginatione0218111
Date Published2019
ISSN1932-6203
Abstract

Late onset Alzheimer's disease is the most common form of dementia for which about 30 susceptibility loci have been reported. The aim of the current study is to identify novel genes associated with Alzheimer's disease using the largest up-to-date reference single nucleotide polymorphism (SNP) panel, the most accurate imputation software and a novel gene-based analysis approach which tests for patterns of association within genes, in the powerful genome-wide association dataset of the International Genomics of Alzheimer's Project Consortium, comprising over 7 million genotypes from 17,008 Alzheimer's cases and 37,154 controls. In addition to earlier reported genes, we detected three novel gene-wide significant loci PPARGC1A (p = 2.2 × 10-6), RORA (p = 7.4 × 10-7) and ZNF423 (p = 2.1 × 10-6). PPARGC1A and RORA are involved in circadian rhythm; circadian disturbances are one of the earliest symptoms of Alzheimer's disease. PPARGC1A is additionally linked to energy metabolism and the generation of amyloid beta plaques. RORA is involved in a variety of functions apart from circadian rhythm, such as cholesterol metabolism and inflammation. The ZNF423 gene resides in an Alzheimer's disease-specific protein network and is likely involved with centrosomes and DNA damage repair.

DOI10.1371/journal.pone.0218111
Pubmed Linkhttps://www.ncbi.nlm.nih.gov/pubmed/31283791?dopt=Abstract
page_expoExternal
Alternate JournalPLoS ONE
PubMed ID31283791
PubMed Central IDPMC6613773
Grant ListMR/K013041/1 / MRC_ / Medical Research Council / United Kingdom
G0300429 / MRC_ / Medical Research Council / United Kingdom
G0902227 / MRC_ / Medical Research Council / United Kingdom
MR/L501517/1 / MRC_ / Medical Research Council / United Kingdom
/ WT_ / Wellcome Trust / United Kingdom
G0600237 / MRC_ / Medical Research Council / United Kingdom

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