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.
Original language | English |
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Pages (from-to) | 142-144 |
Number of pages | 3 |
Journal | Addiction Biology |
Volume | 16 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 2011 |
Keywords
- CYP2B6
- fatalities
- metabolism
- methadone
- OPRM1
- pharmacogenomics
- PLASMA-LEVELS
- PHARMACOKINETICS
- POLYMORPHISMS
- GENOTYPES
- CHANNEL