Genetic polymorphisms of the renin-angiotensin system and obesity-related metabolic changes in response to low-energy diets in obese women

Nutrition. 2011 Jan;27(1):34-39. doi: 10.1016/j.nut.2009.10.012. Epub 2010 Apr 3.

Abstract

Objective: Genetic polymorphisms of the renin-angiotensin system have been implicated in cardiovascular and metabolic diseases. The purpose of this study was to investigate whether the insertion/deletion (I/D) polymorphism of the angiotensin-converting enzyme (ACE) gene and 3123C/A polymorphism of the angiotensin II type 2 receptor (AT(2)R) gene affect blood pressure and other obesity-related metabolic changes in response to low-energy diets using meal replacement shakes for weight loss.

Methods: Clinical, metabolic, and biochemical profiles were measured before and after a 2-mo intervention in 32 obese women (age 49.9 ± 8.4 [SD] y; BMI 28.4 ± 3.3 kg/m²) restricted to 1200 kcal/d (5021 kJ/d). The polymorphisms were determined with an intercalater-mediated FRET probe assay system.

Results: Although weight loss and nutrient intake levels did not differ among the genotypes, the reduction in body fat after weight loss was significantly less in the ACE deletion/deletion (D/D) genotype than insertion/insertion (I/I) plus I/D genotype (-2.25 ± 1.40% versus -0.80 ± 1.57%, P < 0.05). The AT₂R A/A group had significantly less improved levels of systolic blood pressure (-7.23 ± 8.50 versus 2.50 ± 12.6 mmHg, P < 0.05), low-density lipoprotein-cholesterol (-0.36 ± 0.29 versus -0.09 ± 0.25 mmol/L, P < 0.05), carbohydrate (-54.4 ± 27.2 versus -31.8 ± 16.3 mg/min, P < 0.05) and fat oxidation (8.31 ± 11.86 versus 0.05 ± 9.99 mg/min, P < 0.05) than the C/C plus C/A genotypes.

Conclusion: The present findings suggest that the homozygous form of the ACE gene may hinder the improvement of body fat and that the homozygous form of the AT₂R gene may make improving systolic blood pressure and some obesity-related metabolic parameters through a dietary intervention difficult among obese women.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism*
  • Adult
  • Blood Pressure / genetics*
  • Caloric Restriction
  • Carbohydrate Metabolism / genetics
  • Cholesterol, LDL / blood
  • Cholesterol, LDL / genetics
  • Diet, Reducing*
  • Female
  • Genotype
  • Humans
  • Lipid Peroxidation / genetics
  • Middle Aged
  • Obesity / diet therapy
  • Obesity / genetics*
  • Obesity / metabolism
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic*
  • Receptor, Angiotensin, Type 2 / genetics*
  • Renin-Angiotensin System / genetics

Substances

  • Cholesterol, LDL
  • Receptor, Angiotensin, Type 2
  • Peptidyl-Dipeptidase A