Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

TitleGenome-wide association analysis of metabolic traits in a birth cohort from a founder population.
Publication TypeJournal Article
Year of Publication2009
AuthorsSabatti, C, Service SK, Hartikainen A-L, Pouta A, Ripatti S, Brodsky J, Jones CG, Zaitlen NA, Varilo T, Kaakinen M, Sovio U, Ruokonen A, Laitinen J, Jakkula E, Coin L, Hoggart C, Collins A, Turunen H, Gabriel S, Elliot P, McCarthy MI, Daly MJ, Järvelin M-R, Freimer NB, Peltonen L
JournalNature genetics
Volume41
Issue1
Pagination35-46
Date Published2009 Jan
ISSN1546-1718
KeywordsAdult, Blood Pressure, Body Mass Index, Cohort Studies, Finland, Founder Effect, Genome-Wide Association Study, Genotype, Geography, Humans, Linguistics, Metabolic Networks and Pathways, Parturition, Phenotype, Polymorphism, Single Nucleotide, Population Dynamics, Population Groups, Quantitative Trait Loci, Quantitative Trait, Heritable, Reproducibility of Results
Abstract

Genome-wide association studies (GWAS) of longitudinal birth cohorts enable joint investigation of environmental and genetic influences on complex traits. We report GWAS results for nine quantitative metabolic traits (triglycerides, high-density lipoprotein, low-density lipoprotein, glucose, insulin, C-reactive protein, body mass index, and systolic and diastolic blood pressure) in the Northern Finland Birth Cohort 1966 (NFBC1966), drawn from the most genetically isolated Finnish regions. We replicate most previously reported associations for these traits and identify nine new associations, several of which highlight genes with metabolic functions: high-density lipoprotein with NR1H3 (LXRA), low-density lipoprotein with AR and FADS1-FADS2, glucose with MTNR1B, and insulin with PANK1. Two of these new associations emerged after adjustment of results for body mass index. Gene-environment interaction analyses suggested additional associations, which will require validation in larger samples. The currently identified loci, together with quantified environmental exposures, explain little of the trait variation in NFBC1966. The association observed between low-density lipoprotein and an infrequent variant in AR suggests the potential of such a cohort for identifying associations with both common, low-impact and rarer, high-impact quantitative trait loci.

DOI10.1042/AN20110027
Alternate JournalNat. Genet.