抗精神病药物治疗的药物遗传学:最新进展和临床意义。

Molecular Neuropsychiatry Pub Date : 2020-04-01 Epub Date: 2018-09-26 DOI:10.1159/000492332
Kazunari Yoshida, Daniel J Müller
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引用次数: 0

摘要

研究表明,许多基因变异与抗精神病药物反应和精神分裂症治疗的不良反应有关。然而,这些研究结果的临床应用却很有限。本综述旨在总结与抗精神病药物治疗遗传学相关的最新文献和建议,并阐明药物遗传学/药物基因组学(PGx)的临床实用性。我们回顾了有关抗精神病药物 PGx 研究(即抗精神病药物反应和不良反应)以及临床实践中常用商业 PGx 工具的文献。纳入的文献和综述以 2015 年 1 月至 2018 年 4 月间发表的文章为重点。我们发现 44 项研究侧重于抗精神病药物反应,45 项研究侧重于不良反应(如抗精神病药物诱发的体重增加、运动障碍、激素异常和氯氮平诱发的粒细胞减少症/粒细胞减少症),但结果不一。总之,在精神分裂症患者的治疗过程中,已有一些与抗精神病药物反应和不良反应有关的基因变异被报道出来,一些商业药物基因组学检测也已上市。不过,还需要在大量特征明确的样本中进一步开展精心设计的调查和重复研究,以促进 PGx 研究结果在临床实践中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacogenetics of Antipsychotic Drug Treatment: Update and Clinical Implications.

Numerous genetic variants have been shown to be associated with antipsychotic response and adverse effects of schizophrenia treatment. However, the clinical application of these findings is limited. The aim of this narrative review is to summarize the most recent publications and recommendations related to the genetics of antipsychotic treatment and shed light on the clinical utility of pharmacogenetics/pharmacogenomics (PGx). We reviewed the literature on PGx studies with antipsychotic drugs (i.e., antipsychotic response and adverse effects) and commonly used commercial PGx tools for clinical practice. Publications and reviews were included with emphasis on articles published between January 2015 and April 2018. We found 44 studies focusing on antipsychotic response and 45 studies on adverse effects (e.g., antipsychotic-induced weight gain, movement disorders, hormonal abnormality, and clozapine-induced agranulocytosis/granulocytopenia), albeit with mixed results. Overall, several gene variants related to antipsychotic response and adverse effects in the treatment of patients with schizophrenia have been reported, and several commercial pharmacogenomic tests have become available. However, further well-designed investigations and replication studies in large and well-characterized samples are needed to facilitate the application of PGx findings to clinical practice.

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