DBS治疗强迫症抑制默认模式网络。

IF 3.5 2区 医学 Q1 NEUROIMAGING Human Brain Mapping Pub Date : 2024-12-25 DOI:10.1002/hbm.70106
Natalya Slepneva, Genevieve Basich-Pease, Lee Reid, Adam C. Frank, Tenzin Norbu, Andrew D. Krystal, Leo P. Sugrue, Julian C. Motzkin, Paul S. Larson, Philip A. Starr, Melanie A. Morrison, A. Moses Lee
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引用次数: 0

摘要

脑深部电刺激(DBS)的前肢内囊(ALIC)是一种基于电路的治疗严重,难治性强迫症(OCD)。DBS的治疗效果被假设是通过直接调节OCD症状背后的皮质-纹状体-丘脑-皮质分布网络来介导的。然而,DBS发挥其治疗效果的确切潜在机制仍不清楚。在5名因严重难治性强迫症接受DBS治疗的参与者中(3名有反应者,2名无反应者),我们在获得功能MRI(23次fMRI运行)期间进行了DBS开/关循环范式,以确定刺激在各种双极配置中的网络效应。我们还使用弥散加权成像(DWI)进行了神经束造影,将DBS的功能影响与主动刺激接触和功能性脑网络之间的潜在结构连接联系起来。我们发现,与非治疗配置相比,治疗性DBS具有分布式效应,可抑制眼窝前额皮质、背内侧前额皮质和丘脑下核等区域的BOLD活性。治疗性DBS抑制的许多区域是默认模式网络(DMN)的组成部分。此外,从治疗配置中估计的刺激场显示出与DMN核心节点的显著结构连通性。基于这些发现,我们假设ALIC DBS对DMN的抑制是通过DBS活跃接触周围白质结构连接的通信中断介导的。
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Therapeutic DBS for OCD Suppresses the Default Mode Network

Deep brain stimulation (DBS) of the anterior limb of the internal capsule (ALIC) is a circuit-based treatment for severe, refractory obsessive-compulsive disorder (OCD). The therapeutic effects of DBS are hypothesized to be mediated by direct modulation of a distributed cortico-striato-thalmo-cortical network underlying OCD symptoms. However, the exact underlying mechanism by which DBS exerts its therapeutic effects still remains unclear. In five participants receiving DBS for severe, refractory OCD (3 responders, 2 non-responders), we conducted a DBS On/Off cycling paradigm during the acquisition of functional MRI (23 fMRI runs) to determine the network effects of stimulation across a variety of bipolar configurations. We also performed tractography using diffusion-weighted imaging (DWI) to relate the functional impact of DBS to the underlying structural connectivity between active stimulation contacts and functional brain networks. We found that therapeutic DBS had a distributed effect, suppressing BOLD activity within regions such as the orbitofrontal cortex, dorsomedial prefrontal cortex, and subthalamic nuclei compared to non-therapeutic configurations. Many of the regions suppressed by therapeutic DBS were components of the default mode network (DMN). Moreover, the estimated stimulation field from the therapeutic configurations exhibited significant structural connectivity to core nodes of the DMN. Based upon these findings, we hypothesize that the suppression of the DMN by ALIC DBS is mediated by interruption of communication through structural white matter connections surrounding the DBS active contacts.

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来源期刊
Human Brain Mapping
Human Brain Mapping 医学-核医学
CiteScore
8.30
自引率
6.20%
发文量
401
审稿时长
3-6 weeks
期刊介绍: Human Brain Mapping publishes peer-reviewed basic, clinical, technical, and theoretical research in the interdisciplinary and rapidly expanding field of human brain mapping. The journal features research derived from non-invasive brain imaging modalities used to explore the spatial and temporal organization of the neural systems supporting human behavior. Imaging modalities of interest include positron emission tomography, event-related potentials, electro-and magnetoencephalography, magnetic resonance imaging, and single-photon emission tomography. Brain mapping research in both normal and clinical populations is encouraged. Article formats include Research Articles, Review Articles, Clinical Case Studies, and Technique, as well as Technological Developments, Theoretical Articles, and Synthetic Reviews. Technical advances, such as novel brain imaging methods, analyses for detecting or localizing neural activity, synergistic uses of multiple imaging modalities, and strategies for the design of behavioral paradigms and neural-systems modeling are of particular interest. The journal endorses the propagation of methodological standards and encourages database development in the field of human brain mapping.
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