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Branched chain amino acid metabolism and microbiome in adolescents with obesity during weight loss therapy.

McCann, J.; Yang, C.; Bihlmeyer, N.; Tang, R.; Truong, T.; An, J.; Jawahar, J.; Ilkayeva, O.; Muehlbauer, M.; Hu, Z.; Dressman, H. K.; Poppe, L.; Granek, J.; David, L.; Shi, P.; Balikcioglu, P. G.; Shah, S. H.; Armstrong, S. C.; Newgard, C. B.; Seed, P. C.; Rawls, J. F.

2025-02-04 pediatrics
10.1101/2025.02.03.25321363 medRxiv
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BACKGROUNDObesity and weight loss in adults have been associated with distinct metabolome and gut microbiome features, but the extent to which those associations apply to adolescent stages remain unclear. METHODSThe Pediatric Obesity Microbiome and Metabolism Study (POMMS) enrolled 220 adolescents aged 10-18 with severe obesity (OB) and 67 healthy weight controls (HWC). Blood, stool, and clinical measures were collected at baseline and after a 6-month obesity intervention for the OB group. Metabolomic profiling in serum using targeted quantitative mass spectrometry and microbiome profiling in stool were performed, and those features were assessed for associations with BMI, insulin resistance, and inflammation. Fecal microbiome transplants were performed on germ-free mice using samples from both groups to assess effects on weight gain and metabolic pathways. RESULTSAdolescents with OB exhibited higher serum branched-chain amino acid (BCAA) but lower ketoacid metabolite (BCKA) levels compared with HWC. This pattern was sex- and age-dependent, unlike adults with OB, who show elevated levels of both. Longitudinal analysis identified metabolic and microbial features correlated with changes in health measures during the intervention. The fecal microbiomes of adolescents with OB and HWC had similar diversity but differed in membership and functional potential. FMT from both OB and HWC donors had similar effects on mouse body weight, but specific taxa were linked to weight gain in FMT recipients. CONCLUSIONAdolescents with OB have unique metabolomic adaptations and microbiome signatures compared to their HWC counterparts and adults with OB. TRIAL REGISTRATIONClinicalTrials.gov Identifier: NCT03139877 (Observational Study) and NCT02959034 (Repository) FUNDING SOURCESAmerican Heart Association Grants: 17SFRN33670990, 20PRE35180195 National Institute of Diabetes and Digestive and Kidney Diseases Grant: R24-DK110492

Published in Journal of Clinical Investigation (predicted rank #4) · training set

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