Department of Dental Anesthesiology, Tokyo Dental College, 2-9-18 Misaki-cho, Chiyoda-ku, Tokyo 101-0061, Japan; Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan.
Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan.
J Pharmacol Sci. 2018 Mar;136(3):107-113. doi: 10.1016/j.jphs.2018.02.002. Epub 2018 Feb 16.
Opioid analgesics are widely used for the treatment of moderate to severe pain. The analgesic effects of opioids are well known to vary among individuals. The present study focused on the genetic factors that are associated with interindividual differences in pain and opioid sensitivity. We conducted a multistage genome-wide association study in subjects who were scheduled to undergo mandibular sagittal split ramus osteotomy and were not medicated until they received fentanyl for the induction of anesthesia. We preoperatively conducted the cold pressor-induced pain test before and after fentanyl administration. The rs13093031 and rs12633508 single-nucleotide polymorphisms (SNPs) near the LOC728432 gene region and rs6961071 SNP in the tcag7.1213 gene region were significantly associated with the analgesic effect of fentanyl, based on differences in pain perception latency before and after fentanyl administration. The associations of these three SNPs that were identified in our exploratory study have not been previously reported. The two polymorphic loci (rs13093031 and rs12633508) were shown to be in strong linkage disequilibrium. Subjects with the G/G genotype of the rs13093031 and rs6961071 SNPs presented lower fentanyl-induced analgesia. Our findings provide a basis for investigating genetics-based analgesic sensitivity and personalized pain control.
阿片类镇痛药被广泛用于治疗中重度疼痛。阿片类药物的镇痛效果因人而异,这一点是众所周知的。本研究主要关注与疼痛和阿片类药物敏感性个体差异相关的遗传因素。我们对计划接受下颌矢状劈开截骨术的患者进行了多阶段全基因组关联研究,这些患者在接受芬太尼诱导麻醉之前没有接受任何药物治疗。我们在给予芬太尼之前和之后进行了冷加压诱发疼痛测试。在 LOC728432 基因区域附近的 rs13093031 和 rs12633508 单核苷酸多态性(SNP)以及 tcag7.1213 基因区域的 rs6961071 SNP 与芬太尼的镇痛效果显著相关,这是基于芬太尼给药前后疼痛感知潜伏期的差异。我们在探索性研究中确定的这三个 SNP 的关联以前没有报道过。这两个多态性位点(rs13093031 和 rs12633508)表现出很强的连锁不平衡。rs13093031 和 rs6961071 SNP 的 G/G 基因型的受试者表现出较低的芬太尼诱导镇痛作用。我们的发现为研究基于遗传学的镇痛敏感性和个性化疼痛控制提供了基础。