4.5 Article

Changes in the serum metabolite profile in obese children with weight loss

期刊

EUROPEAN JOURNAL OF NUTRITION
卷 54, 期 2, 页码 173-181

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00394-014-0698-8

关键词

Obesity; Childhood; Metabolomics; Metabolite profile; Weight loss; Lifestyle intervention

资金

  1. Commission of the European Communities [FP7-289346-EARLY NUTRITION]
  2. IMI project BIO-MET-Biomarkers, Systems Biology and Phenotypes of the Metabolic Complications of Obesity
  3. German Ministry of Education and Research of the National Genome Research Network, NGFNplus [01 01GI1120A, 01GI 1120B, 001 GI 0825, 01GS0820/01GS0823, 01GI0839]
  4. Systems Biology of Metabotypes project [FKZ 0315494A]
  5. SysMBo
  6. Gani_Med project [03IS206IB]
  7. German Center for Diabetes Research (DZD e.V.)
  8. Helmholtz Zentrum Munchen

向作者/读者索取更多资源

Childhood obesity is an increasing problem and is accompanied by metabolic disturbances. Recently, we have identified 14 serum metabolites by a metabolomics approach (FIA-MS/MS), which showed altered concentrations in obese children as compared to normal-weight children. Obese children demonstrated higher concentrations of two acylcarnitines and lower levels of three amino acids, six acyl-alkyl phosphatidylcholines, and three lysophosphatidylcholines. The aim of this study was to analyze whether these alterations normalize in weight loss. We analyzed the changes of these 14 metabolites by the same metabolic kit as in our previous study in serum samples of 80 obese children with substantial weight loss (BMI-SDS reduction > 0.5) and in 80 obese children with stable weight status all participating in a 1-year lifestyle intervention. In the children without weight change, no significant changes of metabolite concentrations could be observed. In children with substantial weight loss, glutamine, methionine, the lysophosphatidylcholines LPCaC18:1, LPCaC18:2, and LPCa20:4, as well as the acyl-alkyl phosphatidylcholine PCaeC36:2 increased significantly, while the acylcarnitines C12:1 and C16:1, proline, PCaeC34:1, PCaeC34:2, PCaeC34:3, PCaeC36:3, and PCaeC38:2 did not change significantly. The changes of glutamine, methionine, LPCaC18:1, LPCaC18:2, LPCa20:4, and PCaeC36:2 seem to be related to the changes of dieting or exercise habits in lifestyle intervention or to be a consequence of overweight since they normalized in weight loss. Further studies should substantiate our findings.

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