Bastami Salumeh, Gupta Anil, Zackrisson Anna-Lena, Ahlner Johan, Osman Abdimajid, Uppugunduri Srinivas
Unit for Development and Patient Safety, Department of Medical and Health Sciences, Linköping University, Linköping, Sweden.
Basic Clin Pharmacol Toxicol. 2014 Nov;115(5):423-31. doi: 10.1111/bcpt.12248. Epub 2014 May 19.
Therapeutic modulation of pain with morphine and other opioids is associated with significant variation in both effects and adverse effects in individual patients. Many factors including gene polymorphisms have been shown to contribute to the interindividual variability in the response to opioids. The aim of this study was to investigate the significance of UGT2B7, OPRM1 and ABCB1 polymorphisms for interindividual variability in morphine-induced analgesia in patients undergoing hysterectomy. The frequency of these polymorphisms was also investigated in forensic autopsies as morphine is also a very commonly abused drug. Blood samples were collected from 40 patients following abdominal hysterectomy, 24 hr after initiation of analgesia through a patient-controlled analgesia (PCA) pump. Samples were genotyped and analysed for morphine and its metabolites. We also genotyped approximately 200 autopsies found positive for morphine in routine forensic analysis. Patients homozygous for UGT2B7 802C needed significantly lower dose of morphine for pain relief. The same trend was observed for patients homozygous for ABCB1 1236T and 3435T, as well as to OPRM1 118A. The dose of morphine in patients included in this study was significantly related to variation in UGT2B7 T802C. Age was significantly related to both dose and concentration of morphine in blood. Regression analysis showed that 30% of differences in variation in morphine dose could be explained by SNPs in these genes. The genotype distribution was similar between the forensic cases and the patients. However, the mean concentration of morphine was higher in forensic cases compared to patients. We conclude that gene polymorphisms contribute significantly to the variation in morphine concentrations observed in individual patients.
吗啡及其他阿片类药物对疼痛的治疗性调节在个体患者中,其效果和不良反应都存在显著差异。包括基因多态性在内的许多因素已被证明会导致个体对阿片类药物反应的差异。本研究的目的是调查UGT2B7、OPRM1和ABCB1基因多态性对子宫切除患者吗啡诱导镇痛个体差异的意义。由于吗啡也是一种非常常见的滥用药物,因此在法医尸检中也对这些多态性的频率进行了调查。在40例接受腹部子宫切除术的患者中,通过患者自控镇痛(PCA)泵开始镇痛24小时后采集血样。对样本进行基因分型,并分析吗啡及其代谢产物。我们还对在常规法医分析中发现吗啡呈阳性的大约200例尸检进行了基因分型。UGT2B7 802C纯合子患者缓解疼痛所需的吗啡剂量显著较低。ABCB1 1236T和3435T纯合子患者以及OPRM1 118A纯合子患者也观察到相同趋势。本研究中患者的吗啡剂量与UGT2B7 T802C的变异显著相关。年龄与血液中吗啡的剂量和浓度均显著相关。回归分析表明,这些基因中的单核苷酸多态性(SNP)可以解释吗啡剂量变异中30%的差异。法医病例和患者之间的基因型分布相似。然而,法医病例中的吗啡平均浓度高于患者。我们得出结论,基因多态性对个体患者中观察到的吗啡浓度差异有显著贡献。