4.7 Article

Blood Metabolic Signatures of Body Mass Index: A Targeted Metabolomics Study in the EPIC Cohort

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 16, Issue 9, Pages 3137-3146

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.6b01062

Keywords

body mass index; obesity; targeted metabolome; metabolic profiling; blood

Funding

  1. International Agency for Research on Cancer
  2. Fondation de France [2014-00050542]
  3. French National Cancer Institute (L'Institut National du Cancer
  4. INCA) [2009-139]
  5. European Commission (DG-SANCO)
  6. Health Research Fund (FIS) [PI13/00061, PI13/01162]
  7. FEDER
  8. Cancer Research UK [16491, 14136] Funding Source: researchfish
  9. Medical Research Council [G0401527, MR/N003284/1, G1000143, MC_UU_12015/1] Funding Source: researchfish
  10. National Institute for Health Research [NF-SI-0512-10114] Funding Source: researchfish
  11. Novo Nordisk Fonden [NNF14OC0009819] Funding Source: researchfish
  12. MRC [MR/N003284/1, MC_UU_12015/1] Funding Source: UKRI

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Metabolomics is now widely used to characterize metabolic phenotypes associated with lifestyle risk factors such as obesity. The objective of the present study was to explore the associations of body mass index (BMI) with 145 metabolites measured in blood samples in the European Prospective Investigation into Cancer and Nutrition (EPIC) study. Metabolites were measured in blood from 392 men from the Oxford (UK) cohort (EPIC-Oxford) and in 327 control subjects who were part of a nested case-control study on hepatobiliary carcinomas (EPIC-Hepatobiliary). Measured metabolites included amino acids, acylcarnitines, hexoses, biogenic amines, phosphatidylcholines, and sphingomyelins. Linear regression models controlled for potential confounders and multiple testing were run to evaluate the associations of metabolite concentrations with BMI. 40 and 45 individual metabolites showed significant differences according to BMI variations, in the EPIC-Oxford and EPIC-Hepatobiliary subcohorts, respectively. Twenty two individual metabolites (kynurenine, one sphingomyelin, glutamate and 19 phosphatidylcholines) were associated with BMI in both subcohorts. The present findings provide additional knowledge on blood metabolic signatures of BMI in European adults, which may help identify mechanisms mediating the relationship of BMI with obesity-related diseases.

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