Jergas Hannah, Petry-Schmelzer Jan Niklas, Hannemann Jonathan H, Thies Tabea, Strelow Joshua N, Rubi-Fessen Ilona, Quinting Jana, Baldermann Juan Carlos, Mücke Doris, Fink Gereon R, Visser-Vandewalle Veerle, Dembek Till A, Barbe Michael T
Department of Neurology, University Hospital Cologne, Cologne, Germany.
Department of Neurology, University Hospital Cologne, Cologne, Germany
J Neurol Neurosurg Psychiatry. 2025 Mar 13;96(3):280-286. doi: 10.1136/jnnp-2024-333434.
Stimulation-induced dysarthria (SID) is a troublesome and potentially therapy-limiting side effect of deep brain stimulation of the subthalamic nucleus (STN-DBS) in patients with Parkinson's disease (PD). To date, the origin of SID, and especially whether there is an involvement of cerebellar pathways as well as the pyramidal tract, remains a matter of debate. Therefore, this study aims to shed light on structural networks associated with SID and to derive a data-driven model to predict SID in patients with PD and STN-DBS.
Randomised, double-blinded monopolar reviews determining SID thresholds were conducted in 25 patients with PD and STN-DBS. A fibre-based mapping approach, implementing the calculation of fibr-wise ORs for SID, was employed to identify the distributional pattern of SID in the STN's vicinity. The ability of the data-driven model to classify stimulation volumes as 'causing SID' or 'not causing SID' was validated by calculating receiver operating characteristics (ROC) in an independent out-of-sample cohort comprising 14 patients with PD and STN-DBS.
Local fibre-based stimulation maps showed an involvement of fibres running lateral and posteromedial to the STN in the pathogenesis of SID, independent of the investigated hemisphere. ROC analysis in the independent out-of-sample cohort resulted in a good fit of the data-driven model for both hemispheres (area under the curve (AUC)=0.88, AUC=0.88).
This study reveals an involvement of both, cerebello-thalamic fibres, as well as the pyramidal tract, in the pathogenesis of SID in STN-DBS. The results may impact future postoperative programming strategies to avoid SID in patients with PD and STN-DBS TRIAL REGISTRATION NUMBER: DRKS00023221; German Clinical Trials Register (DRKS) Number.
刺激诱发性构音障碍(SID)是帕金森病(PD)患者丘脑底核深部脑刺激(STN-DBS)中一个棘手且可能限制治疗的副作用。迄今为止,SID的起源,尤其是小脑通路以及锥体束是否参与其中,仍存在争议。因此,本研究旨在阐明与SID相关的结构网络,并推导一个数据驱动模型来预测PD和STN-DBS患者的SID。
对25例接受STN-DBS的PD患者进行了随机、双盲单极评估以确定SID阈值。采用基于纤维的映射方法,通过计算SID的纤维方向比值来识别STN附近SID的分布模式。在一个由14例接受STN-DBS的PD患者组成的独立样本外队列中,通过计算受试者工作特征(ROC)曲线来验证数据驱动模型将刺激体积分类为“导致SID”或“不导致SID”的能力。
基于局部纤维的刺激图谱显示,在SID的发病机制中,STN外侧和后内侧走行的纤维参与其中,且与所研究的半球无关。在独立样本外队列中的ROC分析结果显示,数据驱动模型对两个半球的数据拟合良好(曲线下面积(AUC)=0.88,AUC=0.88)。
本研究揭示了小脑-丘脑纤维以及锥体束均参与了STN-DBS中SID的发病机制。这些结果可能会影响未来的术后程控策略,以避免PD和STN-DBS患者出现SID。试验注册号:DRKS00023221;德国临床试验注册中心(DRKS)编号。