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药物基因组学与处方类阿片类药物的使用。

Pharmacogenomics and prescription opioid use.

机构信息

Department of Biotechnology, University of The Western Cape, Robert Sobukwe Road, Bellville 7535, Cape Town, Western Cape, South Africa.

Neuropharmacology on Pain & Functional Diversity (NED), Alicante Institute for Health & Biomedical Research (ISABIAL), Alicante, Spain.

出版信息

Pharmacogenomics. 2021 Mar;22(4):235-245. doi: 10.2217/pgs-2020-0032. Epub 2021 Jan 15.

Abstract

Genome-wide association studies and candidate gene findings suggest that genetic approaches may help in choosing the most appropriate drug and dosage, while preventing adverse drug reactions. This is the field that addresses precision medicine: to evaluate variations in the DNA sequence that could be responsible for different individual analgesic response. We review potential gene biomarkers with best overall convergent functional evidence, for opioid use, in pain management. Polymorphisms can modify pharmacodynamics (i.e., mu opioid receptor, ) and pharmacokinetics (i.e., CYP2D6 phenotypes) pathways altering opioid effectiveness, consumption, side effects or additionally, prescription opioid use dependence vulnerability. This review provides a summary of these candidate variants for the translation of genotype into clinically useful information in pain medicine.

摘要

全基因组关联研究和候选基因研究结果表明,遗传方法可能有助于选择最合适的药物和剂量,同时预防药物不良反应。这就是精准医学所涉及的领域:评估 DNA 序列中的变异,这些变异可能是导致个体对镇痛反应不同的原因。我们综述了在疼痛管理中,具有最佳整体趋同功能证据的潜在基因生物标志物,用于阿片类药物的使用。多态性可以改变药效学(即 μ 阿片受体)和药代动力学(即 CYP2D6 表型)途径,从而改变阿片类药物的有效性、消耗、副作用,或者增加处方阿片类药物使用的依赖易感性。本综述提供了这些候选变体的概述,以便将基因型转化为疼痛医学中具有临床意义的信息。

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