Department of Pharmacology, JIPMER, Puducherry, India.
Department of Anaesthesiology, JIPMER, Puducherry, India.
Anaesthesia. 2019 Nov;74(11):1456-1470. doi: 10.1111/anae.14813. Epub 2019 Aug 27.
Advances in the field of pharmacogenomics have resulted in the discovery of some important single-nucleotide polymorphisms which are found to be associated with opioid dose variability. This, to a large extent, explains genetic variability in the analgesic dose of opioids. These polymorphisms are found in various areas relevant to pain perception, including the nociceptive and antinociceptive pathways, drug receptors, drug-metabolising enzymes and drug efflux molecules. An in-depth knowledge of single-nucleotide polymorphisms can help clinicians to address interindividual variability in opioid dosing and requirements. In the era of precision medicine, these genetic markers can also help us to design prognostic tools to accurately predict the analgesic dose of opioids.
药物基因组学领域的进展发现了一些重要的单核苷酸多态性,这些多态性与阿片类药物剂量的可变性有关。这在很大程度上解释了阿片类药物镇痛剂量的遗传变异性。这些多态性存在于与疼痛感知相关的各个领域,包括伤害感受和抗伤害感受途径、药物受体、药物代谢酶和药物外排分子。深入了解单核苷酸多态性可以帮助临床医生解决阿片类药物剂量和需求的个体间变异性。在精准医学时代,这些遗传标志物还可以帮助我们设计预后工具,准确预测阿片类药物的镇痛剂量。