Abstract
Methadone is used worldwide for the treatment of heroin addiction; however, fatal poisonings are increasingly reported. The prevalence of CYP2B6 and µ-opioid receptor (OPRM1) gene variations were examined between a postmortem population where the deaths were associated with methadone and a live nondrug-using control population using Taqman™ SNP Genotyping assays. The CYP2B6*6 allele was higher in the postmortem population, but the difference was not significant (P = 0.92). The CYP2B6 T750C promoter variation was similar in frequency for both populations. Linkage between T750C and CYP2B6*6 was identified for both populations (P < 0.01). The prevalence of the OPRM1 A118G variation was significantly higher in the control population (P = 0.0046), which might indicate a protective mechanism against opioid toxicity. Individual susceptibility to methadone may be determined by screening for CYP2B6*6.
| Original language | English |
|---|---|
| Pages (from-to) | 431-437 |
| Number of pages | 7 |
| Journal | Journal of Analytical Toxicology |
| Volume | 35 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Sept 2011 |
Keywords
- MU-OPIOID-RECEPTOR
- SINGLE-NUCLEOTIDE POLYMORPHISM
- GENDER-DIFFERENCES
- DOPAMINE RELEASE
- SEX-DIFFERENCES
- ASSOCIATION
- ALCOHOL
- ABUSE
- A118G
- AMPHETAMINE
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