Association between nicotinic acetylcholine receptor single nucleotide polymorphisms and smoking cessation

Nicotine Tob Res. 2012 Aug;14(8):993-7. doi: 10.1093/ntr/ntr246. Epub 2011 Dec 17.

Abstract

Introduction: The α4β2 nicotinic receptor is of central importance in tobacco dependence, while the homomeric α7 receptor may also play a role. In this candidate gene study, we examine the association between 8 single nucleotide polymorphisms (SNPs) in genes coding for nicotinic acetylcholine receptor subunits α4 (rs1044396, rs2273504, rs2236196, and rs2273502), α7 (rs2133965 and rs4779969), and β2 (rs2072660 and rs2072661) and smoking abstinence in a cohort of quitters enrolled in a clinical trial of behavioral support.

Methods: Data were obtained from the "Patch in Practice" study, involving 925 smokers in the United Kingdom. All participants were given an 8-week course of 15 mg of transdermal nicotine replacement therapy and blood was taken for genotyping.

Results: Logistic regression analyses assessed the association between each selected SNP and smoking abstinence at 4, 12, 26, and 52 weeks. There were no statistically significant associations with smoking cessation success or nicotine intake assessed by plasma cotinine levels. However, rs2273502 was associated with a consistent (though nonsignificant) increase in the odds of abstinence.

Conclusions: There was no compelling evidence that these SNPs were associated with a reduced or higher chance of abstinence. However, rs2273502 may be worth investigating in future studies.

Publication types

  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cohort Studies
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Logistic Models
  • Male
  • Middle Aged
  • Nicotine / blood
  • Nicotine / therapeutic use
  • Polymorphism, Single Nucleotide / genetics*
  • Receptors, Nicotinic / genetics*
  • Smoking / therapy
  • Smoking Cessation / statistics & numerical data*
  • Tobacco Use Disorder / genetics*
  • Tobacco Use Disorder / therapy
  • United Kingdom / epidemiology
  • alpha7 Nicotinic Acetylcholine Receptor / genetics*

Substances

  • Nicotine
  • Receptors, Nicotinic
  • alpha7 Nicotinic Acetylcholine Receptor
  • Chrna7 protein, human