Arg347Cys polymorphism of α1a-adrenergic receptor in vasovagal syncope. Case-control study in a Mexican population

Auton Neurosci. 2014 Jul:183:66-71. doi: 10.1016/j.autneu.2014.01.005. Epub 2014 Jan 22.

Abstract

Background: Vasovagal syncope is a common clinical condition, consequential to reduced cerebral blood flow resulting from a failure in cardiovascular homeostasis during orthostasis. Blood pressure regulation is the basis for syncope development. In this regulation, the α1a-adrenergic receptor plays a major role. Some studies have found a positive correlation between the Arg347Cys polymorphism of the α1a-adrenergic receptor to hypertension and heart autonomic control. The goal of this study is to evaluate the possible association between the Arg347Cys α1a-adrenergic receptor polymorphism and vasovagal syncope in a Mexican population.

Methods/major findings: A sample of 89 vasovagal syncope patients and 40 healthy controls were studied. Arg347Cys α1a-adrenergic receptor polymorphism was determined by the PCR-RFLP method. We found an increased frequency of genotype ArgArg in vasovagal syncope patients. In a logistic regression model significant associations were found in two genetic models, in codominant model (OR=13.21: CI 95% 3.69-54.99, p<0.001) and in additive model (OR=12.68: CI 95% 3.5-53.07, p<0.001) for ArgArg genotype with CysCys as reference.

Conclusions: Our data suggests an important participation of Arg347Cys polymorphism as susceptibility factor in patients with vasovagal syncope. ArgArg genotype could be a marker for vasovagal syncope susceptibility in the Mexican population.

Keywords: Adrenergic receptor; Autonomic nervous system; Genes; Syncope.

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Case-Control Studies
  • Child
  • Female
  • Genetic Association Studies
  • Genetic Predisposition to Disease*
  • Genotype
  • Genotyping Techniques
  • Humans
  • Logistic Models
  • Male
  • Mexico
  • Middle Aged
  • Models, Genetic
  • Polymorphism, Single Nucleotide*
  • Receptors, Adrenergic, alpha-1 / genetics*
  • Sex Factors
  • Syncope, Vasovagal / genetics*
  • Young Adult

Substances

  • ADRA1A protein, human
  • Receptors, Adrenergic, alpha-1