深部脑刺激内侧前脑束治疗难治性抑郁症-叙述性文献综述。

Michał Sobstyl, Angelika Stapińska-Syniec
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引用次数: 1

摘要

目的:脑深部电刺激(DBS)是治疗难治性抑郁症(TRD)的一种较新的实验性治疗方式。有初步证据表明,刺激大脑奖赏回路结构或其连接的白质束可能发挥抗抑郁作用。奖励回路的主要核是伏隔核(NAc),它在奖励寻求行为、动机和成瘾中起着关键作用。此外,连接奖励回路不同结构的白质束已被临床研究作为DBS的靶点,包括内侧前脑束(MFB) -中边缘多巴胺能奖励回路的中心组成部分。本综述旨在介绍MFB DBS治疗TRD的临床结果。观点:使用以下关键词对科学文献进行了回顾:'DBS', '重度抑郁症','TRD'和'MFB'。根据患者特征、临床结果和与DBS相关的不良事件对已确定的研究进行评估。搜索显示了5个开放标签临床病例研究和4个病例报告,报告了MFB DBS治疗TRD的累计35例患者。结论:目前MFB DBS的临床数据受样本量小和临床开放标签试验数量少的限制。迫切需要开展更多针对MFB治疗TRD的临床试验。在这些研究中获得的结果表明,在刺激开始后一周内观察到非常迅速的抗抑郁效果。由于其侵袭性,MFB DBS治疗TRD应被视为最后的治疗手段。然而,这种治疗可能是TRD患者的一种有希望的替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression - a narrative literature review.

Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression - a narrative literature review.

Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression - a narrative literature review.

Purpose: Deep brain stimulation (DBS) is a relatively new and still experimental treatment modality for treatment-resistant depression (TRD). There is preliminary evidence that stimulation of brain reward circuit structures or their connecting white matter bundles may exert an antidepressant effect. The main nucleus of the reward circuit is the nucleus accumbens (NAc), which plays a critical role in reward-seeking behavior, motivation, and addiction. Also, white matter bundles connecting different structures of the reward circuit have been studied clinically as targets for DBS, including the medial forebrain bundle (MFB) - a central component of the mesolimbic dopaminergic reward circuit. This review aims to present the clinical outcomes of MFB DBS for TRD.

Views: The scientific literature was reviewed using the following keywords: 'DBS', 'major depressive disorders', 'TRD', and 'MFB'. The identified studies were assessed on the basis of patient characteristics, clinical outcomes, and adverse events related to DBS. The search revealed five open-label clinical case studies and four case reports reporting the cumulative number of 35 patients treated by MFB DBS for TRD.

Conclusions: The current clinical data of MFB DBS are limited by small sample size and the small number of clinical open-label trials. There is an urgent need for more clinical trials targeting the MFB for TRD. The results obtained in these studies showed a very rapid antidepressant effect observed within one week after the start of stimulation. MFB DBS for TRD should be considered as a last resort treatment due to its invasive character. However, this treatment may be a promising alternative for TRD patients.

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