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Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis
Authors:Michael Inouye  Samuli Ripatti  Johannes Kettunen  Leo-Pekka Lyytikäinen  Niku Oksala  Pirkka-Pekka Laurila  Antti J Kangas  Pasi Soininen  Markku J Savolainen  Jorma Viikari  Mika Kähönen  Markus Perola  Veikko Salomaa  Olli Raitakari  Terho Lehtimäki  Marja-Riitta Taskinen  Marjo-Riitta Järvelin  Mika Ala-Korpela  Aarno Palotie  Paul I W de Bakker
Affiliation:Medical Systems Biology, Departments of Pathology and of Microbiology and Immunology, The University of Melbourne, Parkville, Victoria, Australia.
Abstract:Association testing of multiple correlated phenotypes offers better power than univariate analysis of single traits. We analyzed 6,600 individuals from two population-based cohorts with both genome-wide SNP data and serum metabolomic profiles. From the observed correlation structure of 130 metabolites measured by nuclear magnetic resonance, we identified 11 metabolic networks and performed a multivariate genome-wide association analysis. We identified 34 genomic loci at genome-wide significance, of which 7 are novel. In comparison to univariate tests, multivariate association analysis identified nearly twice as many significant associations in total. Multi-tissue gene expression studies identified variants in our top loci, SERPINA1 and AQP9, as eQTLs and showed that SERPINA1 and AQP9 expression in human blood was associated with metabolites from their corresponding metabolic networks. Finally, liver expression of AQP9 was associated with atherosclerotic lesion area in mice, and in human arterial tissue both SERPINA1 and AQP9 were shown to be upregulated (6.3-fold and 4.6-fold, respectively) in atherosclerotic plaques. Our study illustrates the power of multi-phenotype GWAS and highlights candidate genes for atherosclerosis.
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