4.7 Article

Metabolomic Profiles and Childhood Obesity

Journal

OBESITY
Volume 22, Issue 12, Pages 2570-2578

Publisher

WILEY
DOI: 10.1002/oby.20901

Keywords

branched-chain amino acids; androgen; steroid hormones; DHEA-S; metabolomics; obesity; insulin resistance; untargeted

Funding

  1. US National Institutes of Health [K24 HD069408, R37 HD 034568, P30 DK092924]
  2. Thomas O' Pyle Fellowship

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ObjectiveTo identify metabolite patterns associated with childhood obesity, to examine relations of these patterns with measures of adiposity and cardiometabolic risk, and to evaluate associations with maternal peripartum characteristics. MethodsUntargeted metabolomic profiling was used to quantify metabolites in plasma of 262 children (6-10 years). Principal components analysis was used to consolidate 345 metabolites into 18 factors and identified two that differed between obese (BMI95; n=84) and lean children (BMI<85; n=150). The relations of these factors with adiposity (fat mass, BMI, skinfold thicknesses) and cardiometabolic biomarkers (HOMA-IR, triglycerides, leptin, adiponectin, hsCRP, IL-6) using multivariable linear regression was then investigated. Finally, the associations of maternal prepregnancy obesity, gestational weight gain, and gestational glucose tolerance with the offspring metabolite patterns was examined. ResultsA branched-chain amino acid (BCAA)-related pattern and an androgen hormone pattern were higher in obese vs. lean children. Both patterns were associated with adiposity and worse cardiometabolic profiles. For example, each increment in the BCAA and androgen pattern scores corresponded with 6% (95% CI: 1, 13%) higher HOMA-IR. Children of obese mothers had 0.61 (0.13, 1.08) higher BCAA score than their counterparts. ConclusionsBCAA and androgen metabolites were associated with adiposity and cardiometabolic risk during mid-childhood. Maternal obesity may contribute to altered offspring BCAA metabolism.

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