Alzheimer s & Dementia · 2017 · 210 citations · 31 references
Life SciencesGeneticsMolecular GeneticsDementiaGenetic EpidemiologyGenomicsAlzheimer DiseaseDementia GeneticsDisease Susceptibility LociGenome-wide Association StudiesGenotype-phenotype Association AnalysisNeurodegenerative Disease GeneticsApoe GeneticsDementia Risk LociGene-based Association AnalysisGenome-wide Association MappingLocus ArchitectureSingle Nucleotide Polymorphism Association StudiesSingle-nucleotide Polymorphism AnalysisSingle-nucleotide Polymorphism Association Analysis
Abstract Introduction Genetic loci for Alzheimer's disease (AD) have been identified in whites of European ancestry, but the genetic architecture of AD among other populations is less understood. Methods We conducted a transethnic genome‐wide association study (GWAS) for late‐onset AD in Stage 1 sample including whites of European Ancestry, African‐Americans, Japanese, and Israeli‐Arabs assembled by the Alzheimer's Disease Genetics Consortium. Suggestive results from Stage 1 from novel loci were followed up using summarized results in the International Genomics Alzheimer's Project GWAS dataset. Results Genome‐wide significant (GWS) associations in single‐nucleotide polymorphism (SNP)–based tests ( P < 5 × 10 −8 ) were identified for SNPs in PFDN1/HBEGF , USP6NL/ECHDC3 , and BZRAP1‐AS1 and for the interaction of the (apolipoprotein E) APOE ε4 allele with NFIC SNP. We also obtained GWS evidence ( P < 2.7 × 10 −6 ) for gene‐based association in the total sample with a novel locus, TPBG ( P = 1.8 × 10 −6 ). Discussion Our findings highlight the value of transethnic studies for identifying novel AD susceptibility loci.
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