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Genetic variation in mu-opioid-receptor-interacting proteins and smoking cessation in a nicotine replacement therapy trial.

Abstract
Extending a previous finding of an association between functional genetic variation in the mu-opioid receptor gene and response to nicotine replacement therapy, we explored the role of genetic variants in two genes encoding mu-opioid-receptor-interacting proteins, namely ARRB2 and HINT1. Participants were 374 smokers treated for nicotine dependence with either transdermal nicotine or nicotine nasal spray for 8 weeks in an open-label randomized trial. In a logistic regression model controlling for OPRM1 genotype, treatment type, and other covariates, we found no significant main effect of ARRB2 genotype on abstinence at either end of treatment or 6-month follow-up. Participants with the HINT1 TT genotype had significantly higher abstinence rates at 6-month follow-up, but this may not be a pharmacogenetic effect, given that the participants were drug free during this time. Haplotype analysis did not reveal any significant associations for either gene. We found an interaction of ARRB2 and OPRM1 genotype on abstinence at 6 months that approached significance; however, interpretation of this finding is limited by the small number of participants with the minor alleles for both genes. Although these data do not provide support for the role of genetic variation in these mu-opioid-receptor-interacting proteins and smoking cessation, further exploration of opioid pathway genes in larger prospective pharmacogenetic trials may be warranted.
AuthorsRiju Ray, Christopher Jepson, E Paul Wileyto, John P Dahl, Freda Patterson, Margaret Rukstalis, Angela Pinto, Wade Berrettini, Caryn Lerman
JournalNicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco (Nicotine Tob Res) Vol. 9 Issue 11 Pg. 1237-41 (Nov 2007) ISSN: 1462-2203 [Print] England
PMID17978999 (Publication Type: Controlled Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Nicotinic Agonists
  • Receptors, Opioid, mu
  • Nicotine
Topics
  • Adult
  • Female
  • Genetic Variation
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Nicotine (administration & dosage)
  • Nicotinic Agonists (administration & dosage)
  • Receptors, Opioid, mu (genetics)
  • Smoking (genetics)
  • Smoking Cessation (methods)
  • Smoking Prevention
  • Tobacco Use Disorder (drug therapy, genetics)
  • Treatment Outcome

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