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针对治疗抵抗性抑郁症,在扣带回下深部脑刺激中进行个体化靶向治疗是合理的:一项轨迹分析。

Individualized targeting is warranted in subcallosal cingulate gyrus deep brain stimulation for treatment-resistant depression: A tractography analysis.

机构信息

Department of Neurosurgery, Zhejiang University School of Medicine Second Affiliated Hospital, Hangzhou, Zhejiang Province, China.

Clinical Research Center for Neurological Diseases of Zhejiang Province, Hangzhou, China.

出版信息

Hum Brain Mapp. 2023 Aug 1;44(11):4200-4210. doi: 10.1002/hbm.26339. Epub 2023 May 25.

DOI:10.1002/hbm.26339
PMID:37227015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10318244/
Abstract

Subcallosal cingulate gyrus (SCG) is a target of deep brain stimulation (DBS) for treatment-resistant depression. However, previous randomized controlled trials report that approximately 42% of patients are responders to this therapy of last resort, and suboptimal targeting of SCG is a potential underlying factor to this unsatisfactory efficacy. Tractography has been proposed as a supplementary method to enhance targeting strategy. We performed a connectivity-based segmentation in the SCG region via probabilistic tractography in 100 healthy volunteers from the Human Connectome Project. The SCG voxels with maximum connectivity to brain regions implicated in depression, including Brodmann Area 10 (BA10), cingulate cortex, thalamus, and nucleus accumbens were identified, and the conjunctions were deemed as tractography-based targets. We then performed deterministic tractography using these targets in additional 100 volunteers to calculate streamline counts compassing to relevant brain regions and fibers. We also evaluated the intra- and inter-subject variance using test-retest dataset. Two tractography-based targets were identified. Tractography-based target-1 had the highest streamline counts to right BA10 and bilateral cingulate cortex, while tractography-based target-2 had the highest streamline counts to bilateral nucleus accumbens and uncinate fasciculus. The mean linear distance from individual tractography-based target to anatomy-based target was 3.2 ± 1.8 mm and 2.5 ± 1.4 mm in left and right hemispheres. The mean ± SD of targets between intra- and inter-subjects were 2.2 ± 1.2 and 2.9 ± 1.4 in left hemisphere, and 2.3 ± 1.4 and 3.1 ± 1.7 in right hemisphere, respectively. Individual heterogeneity as well as inherent variability from diffusion imaging should be taken into account during SCG-DBS target planning procedure.

摘要

扣带下回(SCG)是深部脑刺激(DBS)治疗抵抗性抑郁症的靶点。然而,先前的随机对照试验报告称,大约 42%的患者对这种最后的治疗方法有反应,而 SCG 的靶向定位不佳是这种疗效不理想的潜在因素。轨迹追踪已被提议作为增强靶向策略的补充方法。我们通过人类连接组计划中的 100 名健康志愿者的概率轨迹追踪在 SCG 区域进行了基于连接的分割。确定了与涉及抑郁的脑区(包括布罗德曼 10 区(BA10)、扣带回皮质、丘脑和伏隔核)具有最大连接性的 SCG 体素,并将这些体素视为基于轨迹追踪的靶点。然后,我们在另外 100 名志愿者中使用这些靶点进行确定性轨迹追踪,以计算包含相关脑区和纤维的流线计数。我们还使用测试-再测试数据集评估了个体内和个体间的方差。确定了两个基于轨迹的靶点。基于轨迹的靶点 1 与右侧 BA10 和双侧扣带皮质的流线计数最高,而基于轨迹的靶点 2 与双侧伏隔核和钩束的流线计数最高。从个体基于轨迹的靶点到解剖学靶点的平均线性距离为左半球 3.2±1.8mm 和右半球 3.2±1.8mm。个体内和个体间的目标平均值±标准偏差分别为左半球 2.2±1.2 和 2.9±1.4,右半球 2.3±1.4 和 3.1±1.7。在 SCG-DBS 靶点规划过程中,应考虑个体内异质性和扩散成像固有的可变性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/0174714c1177/HBM-44-4200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/96a8538d766b/HBM-44-4200-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/ab5e6427768a/HBM-44-4200-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/bc46855c6d1d/HBM-44-4200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/adf58be6dd8a/HBM-44-4200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/0174714c1177/HBM-44-4200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/96a8538d766b/HBM-44-4200-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/ab5e6427768a/HBM-44-4200-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/bc46855c6d1d/HBM-44-4200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/adf58be6dd8a/HBM-44-4200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1371/10318244/0174714c1177/HBM-44-4200-g004.jpg

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