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临床实践中的药物基因组学检测概述。

Overview of pharmacogenomic testing in clinical practice.

作者信息

Gross Tonya, Daniel Jeremy

机构信息

Clinical Psychiatric Pharmacist, Avera Behavioral Health Center, Sioux Falls, South Dakota.

(Corresponding author) Clinical Psychiatric Pharmacist, Avera Behavioral Health Center, Assistant Professor, South Dakota State University College of Pharmacy and Allied Health Professions, Sioux Falls, South Dakota,

出版信息

Ment Health Clin. 2018 Aug 30;8(5):235-241. doi: 10.9740/mhc.2018.09.235. eCollection 2018 Sep.

DOI:10.9740/mhc.2018.09.235
PMID:30206507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6125117/
Abstract

INTRODUCTION

Pharmacogenomic tests relevant to neuropsychiatric medications have been clinically available for more than a decade, but the utility of regular testing is still unknown. Tests available include both pharmacokinetic and pharmacodynamic targets. The potential practice benefits vary with each target.

METHODS

A 10-year literature review was completed utilizing the PubMed database to identify articles relating to the specific pharmacogenomic targets discussed. Further article selection was based on author review for clinical utility.

RESULTS

The clinical dosing guidance available for neuropsychiatric medications such as selective serotonin reuptake inhibitors and tricyclic antidepressants with varying genotypes is useful and has strong evidence to support testing, but it is limited to mainly pharmacokinetic application. Pharmacodynamic targets are gaining additional evidence with increased research, and although the mechanisms behind the potential interactions are scientifically sound, the bridge to clinical practice application is still lacking.

DISCUSSION

Although the benefits of decreasing adverse reactions and improving response time are appealing, clinicians may not utilize pharmacogenomic testing in routine practice due to several barriers. Further clinical guidance and studies are needed to support testing for other neuropsychiatric medications and targets.

摘要

引言

与神经精神药物相关的药物基因组学检测在临床上已应用了十多年,但常规检测的效用仍不明确。现有的检测包括药代动力学和药效学靶点。每个靶点的潜在实践益处各不相同。

方法

利用PubMed数据库完成了一项为期10年的文献综述,以识别与所讨论的特定药物基因组学靶点相关的文章。进一步的文章选择基于作者对临床效用的审查。

结果

针对不同基因型的神经精神药物,如选择性5-羟色胺再摄取抑制剂和三环类抗抑郁药,现有的临床给药指南很有用,并有强有力的证据支持检测,但主要限于药代动力学应用。随着研究的增加,药效学靶点获得了更多证据,尽管潜在相互作用背后的机制在科学上是合理的,但仍缺乏通向临床实践应用的桥梁。

讨论

尽管减少不良反应和缩短反应时间的益处很有吸引力,但由于一些障碍,临床医生可能不会在常规实践中使用药物基因组学检测。需要进一步的临床指导和研究来支持对其他神经精神药物和靶点的检测。

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