Pathophysiology, prognosis and treatment of tardive dyskinesia.

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Therapeutic Advances in Psychopharmacology Pub Date : 2022-10-21 eCollection Date: 2022-01-01 DOI:10.1177/20451253221117313
Hiroyoshi Takeuchi, Yasuhiro Mori, Yuichiro Tsutsumi
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引用次数: 0

Abstract

Tardive dyskinesia (TD), a movement disorder associated with antipsychotics, most frequently affects the lower face and jaw muscles, but can also affect walking, breathing and use of the hands and limbs. Knowledge of TD among physicians may be limited, and the pathophysiology of TD is poorly understood. We conducted this review to summarise the current knowledge surrounding the pathophysiology of TD and present recommendations for prevention and treatment based on a literature search and roundtable discussion attended by psychiatrists in Japan. It has been suggested that dopamine hypersensitivity, damaged gamma-aminobutyric acidergic neurons and/or increased production of reactive oxygen species may contribute to development of TD. Symptoms can profoundly affect everyday life; patients who develop TD have poorer prognoses, worse health-related quality of life, greater social withdrawal and higher mortality than patients without TD. Traditional treatment options include dietary supplements, although evidence for their effectiveness is low. Among pharmaceutical interventions, there is moderate evidence that switching to the second-generation antipsychotic clozapine, which has a lower affinity for dopamine D2 receptors than other antipsychotics, may improve symptoms. Vesicular monoamine transporter 2 (VMAT-2) inhibitors, which oppose the increased dopaminergic activity associated with prolonged antipsychotic use by interfering with dopamine uptake and storage, have the strongest evidence for efficacy. VMAT-2 inhibitors are approved in the United States for the treatment of TD, and the first VMAT-2 inhibitor was approved in Japan for this indication in March 2022. Most guidelines recommend treating TD by first reducing the dose of antipsychotics or switching to clozapine or other second-generation antipsychotics, which have a lower association with TD than first-generation antipsychotics. We recommend focusing on prevention and monitoring for TD when prescribing antipsychotics, given that TD is often irreversible. Physicians should treat with antipsychotics only when necessary and at the lowest effective dose, and frequently monitor for TD symptoms.

Plain language summary: Plain Language Summary (In Japanese).

Visual summary: Visual Summary (In Japanese).

Abstract Image

Abstract Image

Abstract Image

迟发性运动障碍的病理生理学、预后和治疗。
迟发性运动障碍(Tardive dyskinesia,TD)是一种与抗精神病药物相关的运动障碍,最常影响的是下面部和下颌肌肉,但也会影响行走、呼吸以及手和四肢的使用。医生对 TD 的了解可能有限,对 TD 的病理生理学也知之甚少。我们通过文献检索和日本精神科医生参加的圆桌讨论,总结了有关 TD 病理生理学的现有知识,并提出了预防和治疗建议。有研究认为,多巴胺过敏、γ-氨基丁酸能神经元受损和/或活性氧生成增加可能会导致 TD 的发生。症状会严重影响日常生活;与无 TD 的患者相比,患 TD 的患者预后较差,与健康相关的生活质量较差,社交退缩较严重,死亡率较高。传统治疗方法包括膳食补充剂,但其有效性证据不足。在药物干预中,有中等程度的证据表明,改用与多巴胺 D2 受体的亲和力低于其他抗精神病药物的第二代抗精神病药物氯氮平可能会改善症状。囊泡单胺转运体2(VMAT-2)抑制剂通过干扰多巴胺的摄取和储存,抑制因长期服用抗精神病药而增加的多巴胺能活动,其疗效证据最为充分。美国已批准 VMAT-2 抑制剂用于治疗 TD,日本也于 2022 年 3 月批准了首个 VMAT-2 抑制剂用于该适应症。大多数指南建议在治疗 TD 时首先减少抗精神病药物的剂量,或改用氯氮平或其他第二代抗精神病药物,因为与第一代抗精神病药物相比,第二代抗精神病药物与 TD 的相关性较低。鉴于 TD 通常是不可逆的,我们建议在处方抗精神病药物时重点关注 TD 的预防和监测。医生应仅在必要时以最低有效剂量使用抗精神病药物进行治疗,并经常监测TD症状。
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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来源期刊
CiteScore
7.90
自引率
2.40%
发文量
35
审稿时长
10 weeks
期刊介绍: Therapeutic Advances in Psychopharmacology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of psychopharmacology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in psychopharmacology, providing a forum in print and online for publishing the highest quality articles in this area.
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