抄録
To understand the genetics of type 2 diabetes in people of Japanese ancestry, we conducted A meta-analysis of four genome-wide association studies (GWAS; 36,614 cases and 155,150 controls of Japanese ancestry). We identified 88 type 2 diabetes–associated loci (P < 5.0 × 10 −8 ) with 115 independent signals (P < 5.0 × 10 −6 ), of which 28 loci with 30 signals were novel. Twenty-eight missense variants were in linkage disequilibrium (r 2 > 0.6) with the lead variants. Among the 28 missense variants, three previously unreported variants had distinct minor allele frequency (MAF) spectra between people of Japanese and European ancestry (MAF JPN > 0.05 versus MAF EUR < 0.01), including missense variants in genes related to pancreatic acinar cells (GP2) and insulin secretion (GLP1R). Transethnic comparisons of the molecular pathways identified from the GWAS results highlight both ethnically shared and heterogeneous effects of a series of pathways on type 2 diabetes (for example, monogenic diabetes and beta cells).
本文言語 | English |
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ページ(範囲) | 379-386 |
ページ数 | 8 |
ジャーナル | Nature genetics |
巻 | 51 |
号 | 3 |
DOI | |
出版ステータス | Published - 2019 3月 1 |
外部発表 | はい |
ASJC Scopus subject areas
- 遺伝学