| Literature DB >> 31907389 |
Chiu-Ping Fang1, Sheng-Chang Wang1, Hsiao-Hui Tsou2,3, Ren-Hua Chung2, Ya-Ting Hsu2, Shu Chih Liu1, Hsiang-Wei Kuo1, Tung-Hsia Liu1, Andrew C H Chen4,5, Yu-Li Liu6,7.
Abstract
Delta opioid receptor (DOR) is well known to be involved in heroin dependence. This study tested the hypothesis that single nucleotide polymorphisms (SNPs) in the opioid receptor delta 1 (OPRD1) gene coding region are associated with treatment responses in a methadone maintenance therapy (MMT) cohort in Taiwan. Three hundred forty-four MMT patients were recruited. Diastolic/systolic blood pressure, heart rate, methadone dosage, and plasma concentrations of methadone were recorded. Twenty-five SNPs located within the OPRD1 genetic region were selected and genotyped from the genomic DNA of all 344 participants. After pairwise tagger analyses, tagger SNP rs204047 showed a significant association with methadone dosage (P = 0.0019), and tagger SNPs rs204047 and rs797397 were significantly associated with plasma R, S-methadone concentrations (P < 0.0006) in patients tested negative in the urine morphine test, which indicated patients with a better response to MMT. The major genotype carriers showed a higher methadone dosage and higher plasma concentrations of R, S-methadone than the minor genotype carriers. The results indicated that OPRD1 genetic variants were associated with methadone dosage and methadone plasma concentration in MMT patients with a negative morphine test result.Entities:
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Year: 2020 PMID: 31907389 DOI: 10.1038/s10038-019-0718-x
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172