4.6 Article

Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels

期刊

METABOLITES
卷 12, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/metabo12010061

关键词

metabolomics; genome-wise association study; bioresource

资金

  1. Wellcome Trust [212904/Z/18/Z]
  2. Medical Research Council/British Heart Foundation Ancestry and Biological Informative Markers for Stratification of Hypertension (AIMHY) [MR/M016560/1]
  3. European Union (H2020 grants SYSCID) [733100]
  4. Chronic Disease Research Foundation
  5. Zoe Global
  6. NIHR Clinical Research Facility
  7. Biomedical Research Centre (Guy's and St Thomas' NHS Foundation Trust)
  8. MRC AimHy [MR/M016560/1]
  9. National Institute for Health Research Nottingham Biomedical Research Centre
  10. Biomedical Research Centre (King's College London)
  11. Wellcome Trust [212904/Z/18/Z] Funding Source: Wellcome Trust
  12. MRC [MR/M016560/1] Funding Source: UKRI

向作者/读者索取更多资源

This study conducted a genome-wide association study on the levels of circulating metabolites in European subjects, identifying 202 unique genomic regions associated with 478 different metabolites. The replication study confirmed the robustness of these associations and discovered 74 novel genomic regions not previously associated with any metabolites.
Metabolites are small products of metabolism that provide a snapshot of the wellbeing of an organism and the mechanisms that control key physiological processes involved in health and disease. Here we report the results of a genome-wide association study of 722 circulating metabolite levels in 8809 subjects of European origin, providing both breadth and depth. These analyses identified 202 unique genomic regions whose variations are associated with the circulating levels of 478 different metabolites. Replication with a subset of 208 metabolites that were available in an independent dataset for a cohort of 1768 European subjects confirmed the robust associations, including 74 novel genomic regions not associated with any metabolites in previous works. This study enhances our knowledge of genetic mechanisms controlling human metabolism. Our findings have major potential for identifying novel targets and developing new therapeutic strategies.

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