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血清素综合征中药物遗传学的临床相关性

Clinical Relevance of Pharmacogenetics in Serotonin Syndrome.

作者信息

Pandya Dehuti, Tran My, Verduzco-Gutierrez Monica

机构信息

Department of Pharmacy, TIRR Memorial Hermann Hospital, 1333 Moursund St., Houston TX 77030, USA.

University of Texas at Austin, College of Pharmacy, 2409 University Ave., Austin TX 78712, USA.

出版信息

Case Rep Psychiatry. 2020 Oct 7;2020:8860434. doi: 10.1155/2020/8860434. eCollection 2020.

Abstract

Serotonin syndrome is a predictable life-threatening condition that is caused by serotonergic stimulation of the central and peripheral nervous systems. A patient's genetic profile can amplify exposure risk as many serotonergic drugs are metabolized by CYP450 enzymes, and these enzymes may be altered in functionality. We report a case of an elderly man who presented with serotonin syndrome after a dose change in valproic acid 5 weeks prior. His medication list consisted of low-dose serotonergic agents, which is unusual as most cases of serotonin syndrome involve higher doses. A review of his pharmacogenetic profile is presented to retrospectively evaluate the additive risk for serotonin syndrome and implications on resuming serotonergic agents.

摘要

血清素综合征是一种可预测的危及生命的病症,由中枢和外周神经系统的血清素能刺激引起。由于许多血清素能药物由CYP450酶代谢,而这些酶的功能可能发生改变,患者的基因谱会增加暴露风险。我们报告一例老年男性病例,他在5周前丙戊酸剂量改变后出现血清素综合征。他的用药清单包括低剂量血清素能药物,这并不常见,因为大多数血清素综合征病例涉及更高剂量。本文回顾了他的药物遗传学谱,以回顾性评估血清素综合征的附加风险以及恢复使用血清素能药物的影响。

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