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A Polymorphism in the OPRM1 3'-Untranslated Region is Associated with Methadone Efficacy in Treating Opioid Dependence.

Pharmacogenomics Journal 2016 (in press). [doi: 10.1038/tpj.2016.89]

Richard C. Crist, PhD (University of Pennsylvania School of Medicine), Glenn A. Doyle, PhD (University of Pennsylvania School of Medicine), Elliot C. Nelson, MD (Washington University School of Medicine), Louisa Degenhardt, PhD (National Drug and Alcohol Research Centre, Australia), Nicholas G. Martin, PhD (QIMR Berghofer Medical Research Institute, Australia), Grant W. Montgomery, PhD (University of Queensland, Australia), Andrew J. Saxon, MD (VA Puget Sound Health Care System, PN Node), Walter Ling, MD (University of California, Los Angeles, PR Node), Wade H. Berrettini, MD, PhD (University of Pennsylvania School of Medicine).

The mu-opioid receptor (MOR) is the primary target of methadone and buprenorphine. The primary neuronal transcript of the OPRM1 gene, MOR-1, contains a ~13kb 3' untranslated region with five common haplotypes in European-Americans. We analyzed the effects of these haplotypes on the percentage of opioid positive urine tests in European-Americans (n=582) during a 24-week, randomized, open-label trial of methadone or buprenorphine/naloxone (Suboxone) for the treatment of opioid dependence. A single haplotype, tagged by rs10485058, was significantly associated with patient urinalysis data in the methadone treatment group. Methadone patients with the A/A genotype at rs10485058 were less likely to have opioid-positive urine drug screens than those in the combined A/G and G/G genotypes group (relative risk = 0.76, 95% confidence intervals = 0.73-0.80, P=0.0064). Genotype at rs10485058 also predicted self-reported relapse rates in an independent population of Australian patients of European descent (n=1215) who were receiving opioid substitution therapy (P=0.003). In silico analysis predicted that miR-95-3p would interact with the G, but not the A allele of rs10485058, suggesting a potential mechanism for the observed pharmacogenetic effect.

Conclusions: These findings suggest that selection of a medication for opioid dependence based on rs10485058 genotype might improve outcomes in this ethnic group. (Article (Peer-Reviewed), PDF, English, 2016)

Keywords: Buprenorphine/Naloxone | CTN platform/ancillary study | Genetics | Methadone maintenance | Opioid dependence | Pharmacological therapy | Suboxone | Pharmacogenomics Journal (journal)

Document No: 1244, PMID: 27958381.

Submitted by CTN Dissemination Librarians, 12/19/2016.

AUTHORS SEARCH LINK
Berrettini, Wade H. search
Crist, Richard C. search mail
Degenhardt, Louisa search
Doyle, Glenn A. search
Ling, Walter search
Martin, Nicholas G. search
Montgomery, Grant W. search
Nelson, Elliot C. search
Saxon, Andrew J. search mail
PROTOCOLS
NIDA-CTN-0027 www
NIDA-CTN-0027-A-1 www


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Supported by a grant from the National Institute on Drug Abuse to the University of Washington Alcohol and Drug Abuse Institute.
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Updated 12/2016 -- http://ctndisseminationlibrary.org/display/1244.htm
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