Association between β2-adrenoceptor (ADRB2) haplotypes and insulin resistance in PCOS

Clin Endocrinol (Oxf). 2013 Apr;78(4):600-6. doi: 10.1111/cen.12019.

Abstract

Objective: The aim of this study was to explore β2-adrenoceptor (ADRB2) haplotype associations with phenotypes and quantitative traits related to insulin resistance (IR) and the metabolic syndrome (MS) in a polycystic ovary syndrome (PCOS) population. A secondary purpose was to assess the association between ADRB2 haplotype and PCOS.

Design: Genetic polymorphism analysis. Cross-sectional case-control association study.

Setting: Medical University Hospital and research laboratory.

Patients: One hundred and sixty-five unrelated women with PCOS and 116 unrelated women without PCOS (control sample).

Measurements: Clinical and biochemical measurements, and ADRB2 genotyping in PCOS patients and control subjects.

Methods: ADRB2 haplotypes (comprising rs1042711, rs1801704, rs1042713 and rs1042714 in that order), genotyping and statistical analysis to evaluate associations with continuous variables and traits related to IR and MS in a PCOS population. Associations between ADRB2 haplotypes and PCOS were also assessed.

Results: We observed an age-adjusted association between ADRB2 haplotype CCGG and lower insulin (P = 0·018) and HOMA (P = 0·008) in the PCOS sample. Interestingly, the expected differences in surrogate measures of IR between cases and controls were not significant in CCGG/CCGG carriers. In the case-control study, genotype CCGG/CCGG was associated with a 14% decrease in PCOS risk (P = 0·043), taking into account confounding variables.

Conclusions: Haplotype I (CCGG) has a protective role for IR and MS in PCOS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Case-Control Studies
  • Cross-Sectional Studies
  • Female
  • Gene Frequency
  • Genetic Association Studies
  • Haplotypes
  • Humans
  • Insulin Resistance / genetics*
  • Metabolic Syndrome / epidemiology
  • Metabolic Syndrome / genetics
  • Metabolic Syndrome / metabolism
  • Phenotype
  • Polycystic Ovary Syndrome / epidemiology
  • Polycystic Ovary Syndrome / genetics*
  • Polycystic Ovary Syndrome / metabolism
  • Prevalence
  • Receptors, Adrenergic, beta-2 / genetics*
  • Receptors, Adrenergic, beta-2 / metabolism

Substances

  • ADRB2 protein, human
  • Receptors, Adrenergic, beta-2