VMAT2 Inhibitors for Tardive Dyskinesia: What Psychiatrists Should Know.

Focus (American Psychiatric Publishing) Pub Date : 2026-04-01 Epub Date: 2026-04-04 DOI:10.1176/appi.focus.20250044
Arthur N Westover, Jennifer Perez, Zena Patel, Manish K Jha
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Abstract

Tardive dyskinesia (TD) is characterized by involuntary movements that develop in association with chronic use of antipsychotic medications. While second-generation antipsychotics are associated with lower risk of TD compared with first-generation antipsychotics, their widespread use across a range of chronic mental health conditions (such as psychotic disorders, autism, and mood disorders) has resulted in substantial public health burden of TD. The therapeutic landscape of managing TD has been transformed by the U.S. Food and Drug Administration (FDA) approval of two selective vesicular monoamine transporter 2 (VMAT2) inhibitors in 2017. This report reviews efficacy and safety considerations for the two FDA-approved VMAT2 inhibitors, deutetrabenazine and valbenazine, which are recommended as first-line treatment for troublesome TD in current practice guidelines. Overall, these VMAT2 inhibitors offer significant benefit to patients experiencing TD through improved health and quality of life.

VMAT2抑制剂治疗迟发性运动障碍:精神科医生应该知道的
迟发性运动障碍(TD)的特点是与慢性使用抗精神病药物相关的不自主运动。虽然与第一代抗精神病药物相比,第二代抗精神病药物与TD的风险较低相关,但它们在一系列慢性精神健康状况(如精神病、自闭症和情绪障碍)中的广泛使用导致了TD的重大公共卫生负担。2017年,美国食品和药物管理局(FDA)批准了两种选择性囊泡单胺转运蛋白2 (VMAT2)抑制剂,改变了TD的治疗前景。本报告回顾了fda批准的两种VMAT2抑制剂deutetrabenazine和valbenazine的疗效和安全性考虑,这两种抑制剂在目前的实践指南中被推荐作为棘手的TD的一线治疗。总的来说,这些VMAT2抑制剂通过改善健康和生活质量,为TD患者提供了显著的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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