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Defining the anterior nucleus of the thalamus (ANT) as a deep brain stimulation target in refractory epilepsy: Delineation using 3 T MRI and intraoperative microelectrode recording

机译:定义丘脑前核(ANT)作为难治性癫痫的深层脑刺激靶标:使用3 T MRI和术中微电极记录的描绘

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摘要

BACKGROUND:Deep brain stimulation (DBS) is a minimally invasive and reversible method to treat an increasing number of neurological and psychiatric disorders, including epilepsy. Targeting poorly defined deep structures is based in large degree on stereotactic atlas information, which may be a major source of inconsistent treatment effects.AIM OF THE STUDY:In the present study, we aimed to study whether a recently approved target for epilepsy (anterior nucleus of thalamus, ANT) is visualized in clinically established 3 T MRI and whether ANT is delineated using intraoperative microelectrode recording (MER). We have especially focused on individual variation in the location of ANT in stereotactic space. We also aimed to demonstrate the role of individual variation in interpretation of MER data by projecting samples onto AC-PC (anterior and posterior commissure) and ANT-normalized coordinate systems.METHODS:Detailed analysis of ANT delineations in 3 T MRI short tau inversion recovery (STIR) images from eight patients undergoing DBS for refractory epilepsy was performed. Coronal and sagittal cross-sectional models of ANT were plotted in the AC-PC coordinate system to study individual variation. A total of 186 MER samples collected from 10 DBS trajectories and 5 patients were analyzed, and the location of each sample was calculated and corrected accordingly to the location of the final DBS electrode and projected to the AC-PC or coordinate system normalized to ANT.RESULTS:Most of the key structures in the anatomic atlas around ANT (mammillothalamic tract and external medullary lamina) were identified in STIR images allowing visual delineation of ANT. We observed a high degree of anatomical variation in the location of ANT, and the cross-sectional areas overlapped by study patients decreased in a linear fashion with an increasing number of patients. MER information from 10 individual trajectories correlated with STIR signal characteristics by demonstrating a spike-negative zone, presumably white matter layer, at the lateral aspect of ANT in ANT-normalized coordinate system as predicted by STIR images. However, MER information projected to the AC-PC coordinate system was not able to delineate ANT.CONCLUSIONS:ANT is delineated in 3 T MRI by visualization of a thin white matter lamina between ANT and other nuclear groups that lack spiking activity. Direct targeting in the anterior thalamic area is superior to indirect targeting due to extensive individual variation in the location of ANT. Without detailed imaging information, however, a single trajectory MER has little localizing value.
机译:背景:深部脑刺激(DBS)是一种微创且可逆的方法,用于治疗越来越多的神经系统疾病和精神疾病,包括癫痫病。针对定义不明确的深层结构在很大程度上基于立体定位图谱信息,这可能是治疗效果不一致的主要来源。研究目的:在本研究中,我们旨在研究最近是否批准的癫痫(前核)靶标在临床上建立的3 T MRI中可观察到丘脑的ANT),以及是否使用术中微电极记录(MER)描绘了ANT。我们尤其关注于立体定向空间中ANT位置的个体变化。我们还旨在通过将样本投影到AC-PC(前后合缝)和ANT归一化坐标系上来证明个体变异在MER数据解释中的作用。方法:3 T MRI短头倒置恢复中ANT轮廓的详细分析(STIR)图像来自八名接受DBS难治性癫痫治疗的患者。在AC-PC坐标系中绘制ANT的冠状和矢状截面模型,以研究个体差异。分析了从10个DBS轨迹和5位患者收集的总共186个MER样品,计算了每个样品的位置,并根据最终DBS电极的位置进行了校正,并投影到AC-PC或归一化为ANT的坐标系。结果:在STIR图像中可以识别出ANT周围解剖图谱中的大多数关键结构(乳头丘脑束和外延髓层),从而可以直观地描绘出ANT。我们观察到了ANT位置的高度解剖变化,并且研究患者重叠的横截面积随着患者数量的增加呈线性下降。来自10个独立轨迹的MER信息通过在STIR图像所预测的ANT归一化坐标系中的ANT侧面展示了一个尖峰负区域(大概是白质层),与STIR信号特征相关。但是,投影到AC-PC坐标系的MER信息无法描绘出ANT。结论:在3 T MRI中,通过对ANT和其他缺乏突突活性的核群之间的薄白质层进行可视化来描绘ANT。由于ANT位置的个体差异较大,因此在丘脑前部区域进行直接靶向治疗要优于间接靶向治疗。然而,如果没有详细的成像信息,则单个轨迹MER的定位价值很小。

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