4.3 Article

Combined untargeted and targeted metabolomic profiling reveals urinary biomarkers for discriminating obese from normal-weight adolescents

Journal

PEDIATRIC OBESITY
Volume 12, Issue 2, Pages 93-101

Publisher

WILEY
DOI: 10.1111/ijpo.12114

Keywords

Adolescent obesity; biomarker; inflammation; metabolome

Categories

Funding

  1. Civil Research Projects for Solving Social Problems through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [NRF-2013M3C8A2A01078738, NRF-2013M3C8A2A01078732, NRF-2013M3C8A2075911]
  2. Korea National Institute of Health (KNIH) [2012-E64001-00]
  3. Korea Health Promotion Institute [2012-E64001-00] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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BackgroundChildhood and adolescent obesity may lead to obesity and related complications in adulthood. Biomarkers of obesity can be useful for screening for obesity complications and promoting early intervention during school age. Thus, the metabolomic differences in obese children and adolescents should be investigated for identification of potential biomarkers. ObjectivesWe investigated urinary biomarkers to distinguish metabolomic characteristics between obesity and normal weight in adolescents. MethodsAdolescent subjects were divided into non-obese (n=91) and obese (n=93) groups according to body mass index. Untargeted and targeted metabolomic profiling of urine was performed using high-performance liquid chromatography (LC)-quadrupole time-of-flight mass spectrometry (MS), LC-MS/MS and flow injection analysis-MS/MS systems, respectively. ResultsMultivariate statistical analysis showed clear discrimination between the untargeted metabolomes of non-obese and obese groups. Seven endogenous metabolites were distinguished in the obese group, and inflammation-related metabolite markers showed strong predictive power for group classification. From targeted metabolomics, 45 metabolites mostly related to inflammation were significantly different in the obese group. ConclusionsSignificantly different metabolome signatures were identified between normal-weight and obese adolescents. Combined untargeted and targeted metabolomics demonstrated that inflammation-driven insulin resistance, ammonia toxicity and oxidative stress may represent crucial metabolomic signatures in obese adolescents.

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