Different metabolic responses induced by long-term interdisciplinary therapy in obese adolescents related to ACE I/D polymorphism

J Renin Angiotensin Aldosterone Syst. 2017 Apr-Jun;18(2):1470320317703451. doi: 10.1177/1470320317703451.

Abstract

Introduction: The main purpose of the present study was to investigate whether I/D polymorphism of the ACE gene might affect metabolic changes related to the metabolic syndrome through a long-term interdisciplinary therapy in obese adolescents.

Methods: In total, 125 obese adolescents who entered the interdisciplinary obesity programme were assigned to the following two subgroups: metabolic syndrome or non-metabolic syndrome. They were evaluated at baseline and after 1 year. Genomic DNA was extracted from circulating leukocytes.

Results: Subjects with the II genotype in the non-metabolic syndrome group were only to increase their fat-free mass after therapy. Regarding lipid profile, subjects with ID and DD genotypes from both groups reduced their low-density lipoprotein cholesterol levels significantly. The metabolic parameters from the ID and DD genotypes of the non-metabolic syndrome group showed a significantly improved insulin response.

Conclusion: In the present study, we showed that the ACE polymorphism was able to influence the fat-free mass in the I-carry allele in the non-metabolic syndrome group positively. In addition, the I-carry allele was able to improve the insulin resistance of the metabolic syndrome group significantly. These results suggest that the ACE I/D genotypes can influence, in different ways, the specific parameters of metabolism among obese adolescents submitted for long-term interdisciplinary therapy.

Keywords: Interdisciplinary therapy; angiotensin-converting enzyme; metabolic syndrome; obesity; polymorphism.

MeSH terms

  • Adolescent
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease
  • Genotype
  • Homeostasis
  • Humans
  • INDEL Mutation / genetics*
  • Insulin / metabolism
  • Male
  • Models, Biological
  • Obesity / enzymology
  • Obesity / genetics
  • Obesity / metabolism*
  • Obesity / therapy*
  • Patient Care Team*
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic*
  • Risk Factors
  • Young Adult

Substances

  • Insulin
  • ACE protein, human
  • Peptidyl-Dipeptidase A