Insertion/insertion genotype of α(2B)-adrenergic receptor gene polymorphism is associated with silent myocardial ischemia in patients with type 2 diabetes mellitus

Clin Biochem. 2010 Oct;43(15):1201-4. doi: 10.1016/j.clinbiochem.2010.07.023. Epub 2010 Aug 5.

Abstract

Objectives: We investigated whether α(2)-adrenergic receptor (AR) polymorphisms (α(2A)-AR, α(2B)-AR and α(2C)-AR gene) affected silent myocardial ischemia (SMI) in patients with type 2 diabetes mellitus (T2DM).

Design and methods: Genetic polymorphisms were determined in 321 patients with T2DM and coronary artery disease (CAD). Among them, 129 patients experienced transient asymptomatic ST-depression during 24-hour ambulatory electrocardiogram (SMI group), and the remaining 192 patients who had ambulatory electrocardiogram-symptom matching angina were categorized as angina group.

Results: The genotype distribution and allele frequencies of α(2B)-AR gene polymorphism (insertion [I]/deletion[D]) exhibited significant difference between SMI group and angina group (both P < 0.05), with genotype II (34.9%) being higher in SMI group than in angina group (19.8%) (P < 0.01). Multivariable logistic regression analysis revealed that duration of diabetes and genotype II of α(2B)-AR gene polymorphism were independently associated with SMI.

Conclusions: Homozygote for I allele of α(2B)-AR gene polymorphism is associated with SMI in T2DM patients with CAD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Cytokines / blood
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / genetics*
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Multivariate Analysis
  • Mutagenesis, Insertional / genetics*
  • Myocardial Ischemia / blood
  • Myocardial Ischemia / complications*
  • Myocardial Ischemia / genetics*
  • Receptors, Adrenergic, alpha-2 / genetics*
  • Regression Analysis

Substances

  • ADRA2B protein, human
  • Cytokines
  • Receptors, Adrenergic, alpha-2