Identification of metabolic phenotypes in childhood obesity by H NMR metabolomics of blood plasma.

Future Sci OA

Biomolecule Design Group, Institute for Materials Research, Hasselt University, Agoralaan Building D, 3590 Diepenbeek, Belgium.

Published: July 2018

AI Article Synopsis

  • The study aimed to identify the plasma metabolic profile linked to childhood obesity and its different metabolic types.
  • Plasma samples from 65 obese and 37 normal-weight children were analyzed using proton NMR spectroscopy, revealing variations in metabolite concentrations.
  • Results indicated that obese children had elevated lipids and lactate but lower amino acids and glucose levels compared to normal-weight peers; findings suggest potential for using proton NMR metabolomics in diagnosing and understanding childhood obesity.

Article Abstract

Aim: To identify the plasma metabolic profile associated with childhood obesity and its metabolic phenotypes.

Materials & Methods: The plasma metabolic profile of 65 obese and 37 normal-weight children was obtained using proton NMR spectroscopy. NMR spectra were rationally divided into 110 integration regions, which reflect relative metabolite concentrations, and were used as statistical variables.

Results: Obese children show increased levels of lipids, N-acetyl glycoproteins, and lactate, and decreased levels of several amino acids, α-ketoglutarate, glucose, citrate, and cholinated phospholipids as compared with normal-weight children. Metabolically healthy children show lower levels of lipids and lactate, and higher levels of several amino acids and cholinated phospholipids, as compared with unhealthy children.

Conclusion: This study reveals new valuable findings in the field of metabolomics and childhood obesity. Although validation should be performed, the proof of principle looks promising and justifies a deeper investigation of the diagnostic possibilities of proton NMR metabolomics in follow-up studies. NCT03014856. Registered January 9, 2017.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060399PMC
http://dx.doi.org/10.4155/fsoa-2017-0146DOI Listing

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