Suppr超能文献

细胞色素P450 2D6(CYP2D6)基因多态性对当前抗抑郁药剂量推荐的影响。

The impact of the CYP2D6-polymorphism on dose recommendations for current antidepressants.

作者信息

Thuerauf Norbert, Lunkenheimer Jens

机构信息

Department of Psychiatry and Psychotherapy, Friedrich-Alexander-Univeristy of Erlangen-Nuremberg, Schwabachanlage 6, 91054 Erlangen, Germany.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2006 Aug;256(5):287-93. doi: 10.1007/s00406-006-0663-5.

Abstract

Cytochrome P450 CYP2D6 represents an extensively characterized polymorphic drug-metabolizing enzyme. The CYP2D6-gene is highly polymorphic and more than 70 different alleles are known currently. The activity of the enzyme markedly varies among individuals from poor to intermediate and extensive up to ultrarapid metabolism on the basis of the polymorphism of the CYP2D6 gene. Association studies provide growing evidence for the clinical importance of the CYP2D6 polymorphism investigating whether the CYP2D6 genotype distribution differs from that of the normal population either in patients with marked adverse effects or in nonresponders during treatment with CYP2D6 substrates. However, these scientifically important studies present less information for dose adjustments necessary to individualize pharmacotherapy in a given clinical case. With respect to psychopharmacological drug metabolism several antidepressants were characterized as being CYP2D6 substrates. Thus, this review summarizes dose recommendations of current antidepressants.

摘要

细胞色素P450 CYP2D6是一种已被广泛研究的多态性药物代谢酶。CYP2D6基因具有高度多态性,目前已知有70多种不同的等位基因。基于CYP2D6基因的多态性,该酶的活性在个体之间差异显著,从代谢不良到中等代谢、广泛代谢直至超快速代谢。关联研究越来越多地证明了CYP2D6多态性的临床重要性,这些研究调查了在使用CYP2D6底物治疗期间,有明显不良反应的患者或无反应者中,CYP2D6基因型分布是否与正常人群不同。然而,这些具有科学重要性的研究对于在特定临床病例中实现个体化药物治疗所需的剂量调整提供的信息较少。关于精神药物代谢,几种抗抑郁药被确定为CYP2D6底物。因此,本综述总结了当前抗抑郁药的剂量推荐。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验