Association between genetic polymorphisms of beta2 adrenergic receptors and nocturnal asthma in Egyptian children

J Investig Allergol Clin Immunol. 2013;23(4):262-6.

Abstract

Background: Identification of the genetic basis of asthma may contribute to the discovery of effective asthma drugs.

Objective: Our aim was to estimate the association between B2 adrenergic receptor (ADRB2) polymorphisms and nocturnal asthma in Egyptian children.

Methods: ADRB2 polymorphisms Gly16 and Glu27 were genotyped in 200 Egyptian children (90 with nocturnal asthma and 110 healthy controls) using allele-specific polymerase chain reaction.

Results: The homozygous (Gly16) genotype significantly increased the risk of nocturnal asthma (odds ratio [OR], 3.2; 95% CI, 1.3-7.7; P = .003), as did the Gly allele (OR, 1.8: 95% CI, 1.2-2.8).

Conclusions: Our study demonstrated that nocturnal asthma was associated with ADRB2 Arg/Gly polymorphisms but not with ADRB2 Gln/Glu polymorphisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Alleles
  • Amino Acid Substitution
  • Asthma / genetics*
  • Asthma / pathology
  • Case-Control Studies
  • Child
  • Egypt
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Haplotypes
  • Homozygote
  • Humans
  • Male
  • Odds Ratio
  • Polymorphism, Genetic*
  • Receptors, Adrenergic, beta-2 / genetics*

Substances

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