Published in
American Heart Association, Circulation: Cardiovascular Genetics, 6(4), p. 714-715, 2011
DOI: 10.1161/circgenetics.111.962175
Nature Research, Nature, 7362(477), p. 54-60, 2011
DOI: 10.1038/nature10354
Links
- ORCID
- ORCID
- ORCID
- ORCID
- ORCID
- ORCID
- ORCID
- ORCID
- American Heart Association
- Nature Research | PDF
- [push-zb.helmholtz-muenchen.de]
- [mediatum.ub.tum.de] | PDF
- [radar.brookes.ac.uk]
- [radar.brookes.ac.uk]
- [hdl.handle.net]
- [www.researchgate.net] | PDF
- [www.researchgate.net]
- [www.ncbi.nlm.nih.gov] | PDF
- [europepmc.org] | PDF
Tools
Human metabolic individuality in biomedical and pharmaceutical research.
,
B. Wa¨gele,
Ga Wells,
B. Wägele,
T. Zeller,
P. Wild,
He-E. Wichmann,
J. Whitteman,
Karsten Suhre ,
Ak Wagner,
C. Willenborg,
Br Winkelmann,
K. Winkler
and other authors.
Full text: Download
Abstract
Genome-wide association studies (GWAS) have identified many risk loci for complex diseases, but effect sizes are typically small and information on the underlying biological processes is often lacking. Associations with metabolic traits as functional intermediates can overcome these problems and potentially inform individualized therapy. Here we report a comprehensive analysis of genotype-dependent metabolic phenotypes using a GWAS with non-targeted metabolomics. We identified 37 genetic loci associated with blood metabolite concentrations, of which 25 show effect sizes that are unusually high for GWAS and account for 10-60% differences in metabolite levels per allele copy. Our associations provide new functional insights for many disease-related associations that have been reported in previous studies, including those for cardiovascular and kidney disorders, type 2 diabetes, cancer, gout, venous thromboembolism and Crohn's disease. The study advances our knowledge of the genetic basis of metabolic individuality in humans and generates many new hypotheses for biomedical and pharmaceutical research.