OPRM1 rs1799971 polymorphysm and associated factors among opioid-dependent patients undergoing Methadone maintenance therapy
Main Article Content
Abstract
Methadone is an opioid receptor agonist used as substitution therapy for patients with opioid-dependence. Within a multipronged treatment strategy, including evidence-based approaches, genetic characteristics may provide important data related to treatment outcomes. The OPRM1 gene which encodes the µ-opioid receptor (MOR, MOP) – the primary active site of methadone has been extensively studied for its role in vulnerability to substance use disorders and treatment response. This study analyzed OPRM1 gene polymorphysm in 200 patients undergoing methadone maintenance therapy to determine genotype characteristics and related factors in opioid-dependent patient, thereby contributing additional genetic data to the population. In the study population, the G allele frequency was 41.8%, and the genotype distribution was in Hardy–Weinberg equilibrium (χ² = 0.11). In the multivariable regression model, we analyzed factors associated with methadone dose and Alcohol Use Disorders Identification Test – Consumption (AUDIT-C) scores; the analysis showed no clinical factor or OPRM1 genotypes with statistically significant associations (p > 0.05). However, the OPRM1 GG genotype was significantly negatively associated with tobacco use disorder compared with the AA genotype (Coef = −0.893; p = 0.005).
Article Details
Keywords
rs1799971, OPRM1, methadone maintenance treatment, pharmacogenetic
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