首页> 外文期刊>Journal of human genetics >Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence
【24h】

Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence

机译:阿片受体δ1(OPRD1)基因中的遗传多态性与美沙酮维持治疗中的美沙酮剂量有关,用于海洛因依赖性

获取原文
获取原文并翻译 | 示例
           

摘要

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.
机译:众所周知,Delta阿片类受体(DOR)涉及海洛因依赖。该研究测试了阿片类受体δ1(OPRD1)基因编码区的单一核苷酸多态性(SNP)与台湾的美沙酮维持治疗(MMT)队列中的治疗反应相关。招募了三百四十四元患者。记录舒张/收缩压,心率,美沙酮剂量和血浆浓度的美沙酮。选择了25个位于OPRD1遗传区域内的SNP,并从所有344名参与者的基因组DNA中选择并基因分型。在成对标记分析后,标签SNP RS204047显示出与美沙酮剂量的显着关联(P = 0.0019),标签SNPS RS204047和RS797397与尿液中的患者在尿液中进行阴性的血浆R,S-美沙酮浓度(P <0.0006)显着相关吗啡测试,指示患者对MMT的更好反应。主要基因型载体呈较高的甲基剂量和比次要基因型载体的R,S-美沙酮的更高血浆浓度。结果表明,OPRD1遗传变体与MMT患者的甲基遗传变异与含有阴性吗啡检测结果的MMT患者中的美沙酮血浆浓度有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号