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Genetic variability and opioid efficacy

机译:遗传变异性和阿片类药物功效

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A number of clinical observations suggest that patients' genetic disposition influences their response to opioids. This position is strengthened because data from basic research agree with data obtained in human studies. However, a clinical relevance for genetic variability was only established for the CYP2D6 gene polymorphisms and the mu-opioid receptor gene A118G polymorphism. For other opioids or other candidate genes, clinical data are either not available or the data are yet too limited to reach a definitive conclusion. Still, the results obtained so far strongly indicate that opioid efficacy is related to inborn properties caused by genetic variability related to opioid metabolism, opioid receptors, opioid signaling, and opioid transporters. In addition, clinical effects are influenced by variations in other biological systems that modify the effects induced by opioid agonists. Clinical data are lacking for most opioids and little is known about the exact mechanisms by which genetic variability interacts with opioid signaling. Further research should combine basic and clinical research with the end goal of obtaining improved and individualized pain treatment.
机译:许多临床观察表明,患者的遗传倾向会影响他们对阿片类药物的反应。由于基础研究的数据与人体研究获得的数据相符,因此这一立场得到了加强。但是,仅针对CYP2D6基因多态性和μ阿片受体基因A118G多态性建立了遗传变异的临床相关性。对于其他阿片类药物或其他候选基因,要么无法获得临床数据,要么数据太有限而无法得出明确的结论。尽管如此,到目前为止获得的结果仍然强烈表明,阿片类药物的功效与由与阿片类药物代谢,阿片类药物受体,阿片类药物信号传导和阿片类药物转运蛋白有关的遗传变异性引起的先天特性有关。另外,临床效果还受其他生物系统变化的影响,这些变化改变了阿片类激动剂诱导的效果。大多数阿片类药物缺乏临床数据,并且关于遗传变异性与阿片类药物信号传导相互作用的确切机制知之甚少。进一步的研究应将基础研究和临床研究结合起来,最终目标是获得改善的个性化疼痛治疗。

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