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.

译文

:与美沙酮有关的死亡中,最大比例的死亡发生在药物诱导阶段。我们分析了与美沙酮作用相关的基因变异与美沙酮相关的致命性。发现高美沙酮浓度与慢代谢者表型的CYP2B6 * 6等位基因特征之间存在显着关联。我们建议美沙酮死亡的风险可能是由CYP2B6 * 6等位基因部分确定的。在与美沙酮有关的死亡中,死后苯二氮卓类药物的浓度与OPRM1 A118G等位基因GA之间也观察到显着相关性。在美沙酮处方前对这些药敏性变化进行筛查可以帮助减少发生严重不良反应的可能性。

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