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ABSTRACT: Background
Data are limited on genome-wide association studies (GWAS) for incident coronary heart disease (CHD). Moreover, it is not known whether genetic variants identified to date also associate with risk of CHD in a prospective setting.Methods
We performed a two-stage GWAS analysis of incident myocardial infarction (MI) and CHD in a total of 64,297 individuals (including 3898 MI cases, 5465 CHD cases). SNPs that passed an arbitrary threshold of 5×10-6 in Stage I were taken to Stage II for further discovery. Furthermore, in an analysis of prognosis, we studied whether known SNPs from former GWAS were associated with total mortality in individuals who experienced MI during follow-up.Results
In Stage I 15 loci passed the threshold of 5×10-6; 8 loci for MI and 8 loc
SUBMITTER: Dehghan A
PROVIDER: S-EPMC4780701 | biostudies-literature | 2016
REPOSITORIES: biostudies-literature