四个阿根廷人群中pdyn和oprk1基因的变异及其与急性术后疼痛相关临床变量的遗传关联

G. P. Di Santo Meztler, J. Schiaffi, A. Rigalli, M. E. Esteban Torné, P. Martina, C. I. Catanesi
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引用次数: 0

摘要

一些人群研究表明,疼痛敏感性的变化与人类前啡肽(PDYN)和Kappa阿片受体(OPRK1)基因的遗传多态性之间存在关联。我们分析了这两个基因的多态性,以表征它们在阿根廷人群中的变异,并评估它们与急性疼痛敏感性的关系。我们研究了来自阿根廷四个地点(Ciudad Autónoma de Buenos Aires, La Plata, Resistencia和Misión Nueva Pompeya)个体的11个遗传标记,计算了群体参数,并通过广义估计方程模型评估了疼痛敏感性,临床和遗传变量之间的可能关联。这两个基因在4个种群中均存在高度的连锁不平衡,并且在阿根廷种群中发现的频率与1000基因组计划中报告的其他大陆种群的频率存在显著差异。来自3′非翻译区和外显子4的4个PDYN基因多态性与急性疼痛敏感性相关。每种多态性的一种基因型与较高的疼痛敏感性相关,可能与n -甲基- d -天冬氨酸(NMDA)受体的激活有关。我们发现以下临床变量与急性疼痛密切相关:1)手术后时间,2)每8小时静脉注射氯西多尔,3)切口类型。我们的结果强调了影响疼痛敏感性和镇痛反应的遗传变异区域研究的重要性。关键词:人群,疼痛敏感性,急性疼痛,遗传多态性,遗传结构
本文章由计算机程序翻译,如有差异,请以英文原文为准。
VARIABILITY OF PDYN AND OPRK1 GENES IN FOUR ARGENTINIAN POPULATIONS AND ITS GENETIC ASSOCIATION WITH CLINICAL VARIABLES RELATED TO ACUTE POSTSURGICAL PAIN
Several population studies showed an association between variation in pain sensitivity and genetic polymorphisms located in Prodynorphin (PDYN) and Kappa Opioid Receptor (OPRK1) human genes. We analysed polymorphisms of these two genes to characterise their variation in Argentinian populations, as well as to evaluate their association with acute pain sensitivity. We studied 11 genetic markers in individuals from four locations in Argentina (Ciudad Autónoma de Buenos Aires, La Plata, Resistencia, and Misión Nueva Pompeya), calculated the population parameters, and evaluated the possible association among pain sensitivity, clinical, and genetic variables through a Generalised Estimating Equation model. High linkage disequilibrium was observed in the four populations for both genes, and significant differences were found among frequencies of Argentinian populations and those from other continents reported in the 1000 Genomes Project. Four PDYN gene polymorphisms from 3´ untranslated region and exon 4 showed association with acute pain sensitivity. One genotype of each of these polymorphisms was associated with a higher pain sensitivity, probably related with the activation of the N-methyl-D-aspartate (NMDA) receptors. We found a strong association with acute pain for the following clinical variables: 1) time after surgery, 2) intravenous klosidol supplied every 8 h, and 3) type of incision. Our results highlight the importance of a regional study of genetic variants which influence pain sensitivity and analgesic response. Key words: human populations, pain sensitivity, acute pain, genetic polymorphisms, genetic structure
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