An environmental epigenetic study of ADRB2 5'-UTR methylation and childhood asthma severity

Clin Exp Allergy. 2012 Nov;42(11):1575-81. doi: 10.1111/j.1365-2222.2012.04055.x. Epub 2012 Aug 3.

Abstract

Background: Beta-2 adrenergic receptor (ADRB2) is the primary target of both short- and long-acting beta-agonist asthma medications. ADRB2 5'-UTR methylation changes in blood have the potential to act as a surrogate biomarker of responsiveness to beta-agonist treatment and childhood asthma severity.

Objective: To study the association between ADRB2 5'-UTR methylation, NO (2) exposure and childhood asthma severity.

Methods: We compared ADRB2 5'-UTR methylation levels in blood between 60 children with mild asthma and 122 children with severe asthma using methylation-specific PCR. We also investigated potential joint effects between NO (2) exposure and ADRB2 5'-UTR methylation.

Results: We found a significant association between intermediate (OR: 4.11, 95% CI: 1.58-10.73) and high levels (OR: 7.63, 95% CI: 3.02-19.26) of ADRB2 methylation and severe childhood asthma. In addition, we found a significant association between indoor exposure to NO (2) , an air pollutant and known asthmogen, and severe asthma among children exhibiting high ADRB2 methylation (OR: 4.59, 95% CI: 1.03-20.55) but no association among children exhibiting low levels of ADRB2 methylation (OR: 0.35, 95% CI: 0.01-14.13).

Conclusions and clinical relevance: These findings support the potential use of ADRB2 5'-UTR methylation as a biomarker of both asthma severity and risk for NO (2) -associated asthma exacerbations in children, and present the first evidence of an epigenetic link between an important environmental exposure and childhood asthma severity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5' Untranslated Regions*
  • Adolescent
  • Asthma / etiology*
  • Asthma / genetics
  • Child
  • Child, Preschool
  • CpG Islands
  • DNA Methylation*
  • Environmental Exposure*
  • Epigenesis, Genetic*
  • Female
  • Gene-Environment Interaction
  • Humans
  • Male
  • Nitrogen Dioxide*
  • Receptors, Adrenergic, beta-2 / genetics*
  • Risk
  • Severity of Illness Index

Substances

  • 5' Untranslated Regions
  • Receptors, Adrenergic, beta-2
  • Nitrogen Dioxide