通过导航经颅磁刺激对神经胶质瘤患者辅助运动区进行定位,推进运动系统的术前评估。

IF 3 2区 医学 Q2 CLINICAL NEUROLOGY
Maximilian Schwendner, Haosu Zhang, Leonie Kram, Sandro M Krieg, Sebastian Ille
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引用次数: 0

摘要

目的:切除额上回内的胶质瘤可导致延长,在某些情况下,持续的辅助运动区(SMA)综合征。这突出了准确识别皮层SMA及其下纤维束的必要性。在这项研究中,作者利用导航经颅磁刺激(nTMS)作图和基于功能的纤维束束造影来描绘额叶脑肿瘤患者的SMA。方法:对额上回内SMA前区和SMA正区6个刺激靶点进行连续θ波爆发刺激。患者在刺激时使用对侧的手进行九孔钉试验。结果:研究纳入22例患者,平均年龄47.7±17.3(25.3-79.4)岁,无运动功能障碍(11例低级别胶质瘤,11例高级别胶质瘤),其中12例(54.5%)为左侧病变。在两个半球上观察到的tms阳性定位相同(右侧:中位数3[范围2-4]vs左侧:中位数3[范围1-4],p = 0.694)。6例患者(27.3%)术后出现延长的SMA综合征,并持续3个月随访检查。此外,1例患者(4.5%)表现出与主要运动区相关的永久性运动缺陷。在延长的SMA综合征患者中,切除的ntms阳性SMA部位的数量明显更高,中位数为2(范围2-3),而非SMA综合征患者的中位数为0(范围0-2)(p = 0.004)。切除ntms阳性的SMA点对发生延长期SMA综合征的敏感性为100%,特异性为73.3%。在皮质下水平,切除额斜束(FAT)的特异性最高(0.867),阴性预测值为0.929。结合FAT和额纹状体束的结果,特异性为0.667,敏感性和阴性预测值为1.00。结论:基于tms的SMA定位是可行、准确和可靠的。切除ntms阳性皮质部位和皮层下纤维束对延长性SMA综合征的发生具有极好的敏感性和阴性的预测价值。然而,目前这些数据还不足以完全阐明SMA综合征的发生。除了nTMS运动定位外,还应在运动障碍脑病变中进行基于tms导航的SMA定位,以识别高危患者并优化手术结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancing preoperative assessment of the motor system through navigated transcranial magnetic stimulation-based mapping of the supplementary motor area in patients with glioma.

Objective: Resection of gliomas within the superior frontal gyrus can result in prolonged and, in some cases, persistent supplementary motor area (SMA) syndrome. This highlights the need to accurately identify the cortical SMA and its underlying fiber tracts. In this study, the authors utilized navigated transcranial magnetic stimulation (nTMS) mapping and function-based fiber tractography to delineate the SMA in patients with frontal brain tumors.

Methods: Continuous theta burst stimulation was performed over six stimulation targets in the pre-SMA and SMA proper within the superior frontal gyrus. Patients performed the nine-hole peg test during stimulation using the hand contralateral to the stimulation.

Results: The study included 22 patients with a mean age of 47.7 ± 17.3 (range 25.3-79.4) years without motor deficits (11 low-grade gliomas, 11 high-grade gliomas), 12 (54.5%) of whom had left-sided lesions. Navigated TMS-positive sites were observed equally on both hemispheres (right: median 3 [range 2-4] vs left: median 3 [range 1-4], p = 0.694). Six patients (27.3%) developed a prolonged SMA syndrome postoperatively, persisting at the 3-month follow-up examination. Additionally, 1 patient (4.5%) exhibited permanent motor deficits related to the primary motor area. In patients with prolonged SMA syndrome, the number of resected nTMS-positive SMA sites was significantly higher, with a median of 2 (range 2-3) compared with 0 (range 0-2) in patients without SMA syndrome (p = 0.004). Resection of nTMS-positive SMA points showed a sensitivity of 100% and a specificity of 73.3% for the occurrence of a prolonged SMA syndrome. On the subcortical level, resection of the frontal aslant tract (FAT) showed the highest specificity (0.867) and negative predictive value (0.929). Combining findings of the FAT and frontostriatal tract resulted in a specificity of 0.667, with a sensitivity and negative predictive value of 1.00.

Conclusions: Navigated TMS-based mapping of the SMA is feasible, accurate, and reliable. Resection of nTMS-positive cortical sites and underlying subcortical fiber tracts provides excellent sensitivity and negative predictive value for the occurrence of prolonged SMA syndrome. However, these data are currently insufficient to fully elucidate the occurrence of SMA syndrome. Navigated TMS-based mapping of the SMA should be performed in addition to nTMS motor mapping in motor eloquent brain lesions to identify at-risk patients and optimize surgical outcomes.

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来源期刊
Neurosurgical focus
Neurosurgical focus CLINICAL NEUROLOGY-SURGERY
CiteScore
6.30
自引率
0.00%
发文量
261
审稿时长
3 months
期刊介绍: Information not localized
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