Association of µ-opioid receptor (OPRM1) gene polymorphism with response to naltrexone in alcohol dependence: a systematic review and meta-analysis
- PMID: 22515274
- DOI: 10.1111/j.1369-1600.2012.00442.x
Association of µ-opioid receptor (OPRM1) gene polymorphism with response to naltrexone in alcohol dependence: a systematic review and meta-analysis
Abstract
Previous studies have suggested that the effect of naltrexone in patients with alcohol dependence may be moderated by genetic factors. In particular, the possession of the G allele of the A118G polymorphism of the µ-opioid receptor gene (OPRM1) has been associated with a better response to naltrexone, although controversial results have been reported. The aim of this paper is to combine previous findings by means of a systematic review and a meta-analysis. We retrieved studies on the relationship between A118G polymorphism in OPRM1 gene and response to treatment with naltrexone in patients with alcohol dependence by means of electronic database search. A meta-analysis was conducted using a random-effects model. Calculations of odds ratio (OR) and their confidence intervals (CI) and tests for heterogeneity of the results have been performed. Six previous studies have analyzed the role of A118G polymorphism in response to naltrexone for alcohol dependence. After meta-analysis, we found that naltrexone-treated patients carrying the G allele had lower relapse rates than those who were homozygous for the A allele (OR: 2.02, 95% CI 1.26-3.22; P = 0.003). There were no differences in abstinence rates. Our results support the fact that the G allele of A118G polymorphism of OPRM1 moderates the effect of naltrexone in patients with alcohol dependence. This genetic marker may therefore identify a subgroup of individuals more likely to respond to this treatment.
© 2012 The Authors, Addiction Biology © 2012 Society for the Study of Addiction.
Similar articles
-
An evaluation of mu-opioid receptor (OPRM1) as a predictor of naltrexone response in the treatment of alcohol dependence: results from the Combined Pharmacotherapies and Behavioral Interventions for Alcohol Dependence (COMBINE) study.Arch Gen Psychiatry. 2008 Feb;65(2):135-44. doi: 10.1001/archpsyc.65.2.135. Arch Gen Psychiatry. 2008. PMID: 18250251 Free PMC article. Clinical Trial.
-
[A pharmacogenetic analysis of dopaminergic and opioidergic genes in opioid addicts treated with the combination of naltrexone and guanfacine].Zh Nevrol Psikhiatr Im S S Korsakova. 2016;116(11. Vyp. 2):36-48. doi: 10.17116/jnevro201611611236-48. Zh Nevrol Psikhiatr Im S S Korsakova. 2016. PMID: 28300812 Clinical Trial. Russian.
-
A micro opioid receptor gene polymorphism (A118G) and naltrexone treatment response in adherent Korean alcohol-dependent patients.Psychopharmacology (Berl). 2009 Jan;201(4):611-8. doi: 10.1007/s00213-008-1330-5. Epub 2008 Sep 16. Psychopharmacology (Berl). 2009. PMID: 18795264 Clinical Trial.
-
Lack of associations of the opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with alcohol dependence: review and meta-analysis of retrospective controlled studies.BMC Med Genet. 2017 Oct 26;18(1):120. doi: 10.1186/s12881-017-0478-4. BMC Med Genet. 2017. PMID: 29070014 Free PMC article. Review.
-
Influence of the OPRM1 A118G polymorphism on alcohol-induced euphoria, risk for alcoholism and the clinical efficacy of naltrexone.Pharmacogenomics. 2012 Jul;13(10):1161-72. doi: 10.2217/pgs.12.99. Pharmacogenomics. 2012. PMID: 22909206 Review.
Cited by
-
Neural and behavioral effects of a novel mu opioid receptor antagonist in binge-eating obese people.Biol Psychiatry. 2013 May 1;73(9):887-94. doi: 10.1016/j.biopsych.2012.10.022. Epub 2012 Dec 14. Biol Psychiatry. 2013. PMID: 23245760 Free PMC article. Clinical Trial.
-
Transcranial Magnetic Stimulation and Deep Brain Stimulation in the treatment of alcohol dependence.Addict Disord Their Treat. 2014 Dec;13(4):159-169. doi: 10.1097/ADT.0b013e31829cf047. Addict Disord Their Treat. 2014. PMID: 25598743 Free PMC article.
-
Alcohol use disorder: pathophysiology, effects, and pharmacologic options for treatment.Subst Abuse Rehabil. 2014 Jan 23;5:1-12. doi: 10.2147/SAR.S37907. eCollection 2014. Subst Abuse Rehabil. 2014. PMID: 24648792 Free PMC article. Review.
-
Pharmacotherapy of alcohol use disorders: seventy-five years of progress.J Stud Alcohol Drugs Suppl. 2014;75(17):79-88. doi: 10.15288/jsads.2014.s17.79. J Stud Alcohol Drugs Suppl. 2014. PMID: 24565314 Free PMC article. Review.
-
Using naltrexone to validate a human laboratory test system to screen new medications for alcoholism (TESMA)- a randomized clinical trial.Transl Psychiatry. 2023 Apr 5;13(1):113. doi: 10.1038/s41398-023-02404-7. Transl Psychiatry. 2023. PMID: 37019884 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases