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CYP2B6 and OPRM1 gene variations predict methadone-related deaths.
- Source :
-
Addiction biology [Addict Biol] 2011 Jan; Vol. 16 (1), pp. 142-4. - Publication Year :
- 2011
-
Abstract
- The largest proportion of methadone-associated deaths occurs during the drug induction phase. We analysed methadone-related fatalities for gene variations linked with methadone action. A significant association between high methadone concentrations and the CYP2B6*6 allele characteristic of the slow metabolizer phenotype was identified. We suggest that the risk of methadone fatality may be predetermined in part by the CYP2B6*6 allele. A significant correlation was also observed between post-mortem benzodiazepine concentrations and the OPRM1 A118G allele GA in methadone-related fatalities. Screening for these susceptibility variations prior to methadone prescription could assist in reducing the potential for serious adverse effects.
- Subjects :
- Benzodiazepines pharmacokinetics
Benzodiazepines toxicity
Cause of Death
Cytochrome P-450 CYP2B6
Drug Synergism
Gene Frequency genetics
Genetic Carrier Screening
Genetic Predisposition to Disease genetics
Genetic Testing
Heroin Dependence blood
Humans
Methadone pharmacokinetics
Morphine pharmacokinetics
Narcotics pharmacokinetics
Risk Factors
Alleles
Aryl Hydrocarbon Hydroxylases genetics
Genetic Variation genetics
Genotype
Heroin Dependence mortality
Heroin Dependence rehabilitation
Methadone toxicity
Narcotics toxicity
Opiate Substitution Treatment adverse effects
Opiate Substitution Treatment mortality
Oxidoreductases, N-Demethylating genetics
Receptors, Opioid, mu genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1369-1600
- Volume :
- 16
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Addiction biology
- Publication Type :
- Academic Journal
- Accession number :
- 21158011
- Full Text :
- https://doi.org/10.1111/j.1369-1600.2010.00274.x