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丘脑底核深部脑刺激对具有遗传风险因素/病因的帕金森病患者的影响研究。

Investigation of the Impact of Deep Brain Stimulation of the Subthalamic Nucleus on Parkinson Disease Patients with Genetic Risk Factors/Causes.

作者信息

Wu Sheng, Cen Zhidong, Zheng Xiaosheng, Xie Fei, Luo Wei

机构信息

Department of Neurology, Second Affiliated Hospital of Zhejiang University, Hangzhou, China.

Department of Neurology, Sir Run Run Shaw Hospital of Zhejiang University, Hangzhou, China.

出版信息

World Neurosurg. 2025 Jun;198:124021. doi: 10.1016/j.wneu.2025.124021. Epub 2025 Apr 26.

Abstract

OBJECTIVE

The impact of deep brain stimulation of the subthalamic nucleus (STN-DBS) on patients with Parkinson disease (PD) with different genetic risk factors/causes remains uncertain. This study aimed to compare the clinical efficacy of STN-DBS in these patients.

METHODS

This study compared STN-DBS outcomes in 18 PD patients with mutations in glucosylceramidase beta (GBA) (n = 3), leucine-rich repeat kinase 2 (LRRK2) (n = 9), or Parkin RBR E3 ubiquitin ligase/PTEN-induced kinase 1/DJ1 (n = 6). Clinical measures-levodopa equivalent daily dose, Movement Disorder Society Unified-Parkinson Disease Rating Scale Part III, Parkinson's Disease Questionnaire-39 (PDQ-39), and total electrical energy delivered-were assessed at baseline, programming initiation, 6 months, 1 year, and 2 years postsurgery. Linear mixed models analyzed longitudinal and intergroup differences.

RESULTS

All groups showed significant time-dependent improvements. Levodopa equivalent daily dose dropped sharply post-DBS (maximal reduction at 1 year: β = -577.33, P < 0.001). Movement Disorder Society Unified-Parkinson Disease Rating Scale Part III scores improved by programming initiation (β = -35.00, P < 0.001) and remained stable for 2 years. PDQ-39 scores improved from 6 months onward (β = -27.67, P < 0.001). Total electrical energy delivered increased gradually, with LRRK2 carriers requiring higher stimulation by 2 years (time × gene interaction: β = 94.21, P = 0.043). Main effects revealed GBA carriers had smaller motor improvements (vs. LRRK2: β = -24.94, P = 0.001; vs. Parkin RBR E3 ubiquitin ligase/PTEN-induced kinase 1/DJ1: β = -23.61, P = 0.008) and lesser PDQ-39 gains (β = -22.67, P = 0.018).

CONCLUSIONS

STN-DBS demonstrated benefits for patients with PD across all genetic backgrounds, but LRRK2 carriers may require increasing stimulation over time, while GBA carriers show reduced motor and quality-of-life improvements.

摘要

目的

丘脑底核深部脑刺激术(STN-DBS)对具有不同遗传风险因素/病因的帕金森病(PD)患者的影响仍不确定。本研究旨在比较STN-DBS在这些患者中的临床疗效。

方法

本研究比较了18例分别携带葡糖脑苷脂酶β(GBA)突变(n = 3)、富含亮氨酸重复激酶2(LRRK2)突变(n = 9)或帕金RBR E3泛素连接酶/PTEN诱导激酶1/DJ1突变(n = 6)的PD患者接受STN-DBS后的结果。在基线、编程开始时、术后6个月、1年和2年评估临床指标——左旋多巴等效日剂量、运动障碍协会统一帕金森病评定量表第三部分、帕金森病问卷-39(PDQ-39)以及总传递电能。采用线性混合模型分析纵向和组间差异。

结果

所有组均显示出显著的时间依赖性改善。STN-DBS后左旋多巴等效日剂量急剧下降(1年时最大降幅:β = -577.33,P < 0.001)。运动障碍协会统一帕金森病评定量表第三部分评分在编程开始时有所改善(β = -35.00,P < 0.001),并在2年内保持稳定。PDQ-39评分从6个月起开始改善(β = -27.67,P < 0.001)。总传递电能逐渐增加,LRRK2突变携带者在2年时需要更高的刺激量(时间×基因交互作用:β = 94.21,P = 0.043)。主要效应显示,GBA突变携带者的运动改善较小(与LRRK2突变携带者相比:β = -24.94,P = 0.001;与帕金RBR E3泛素连接酶/PTEN诱导激酶1/DJ1突变携带者相比:β = -23.61,P = 0.008),PDQ-39评分增加较少(β = -22.67,P = 0.018)。

结论

STN-DBS对所有遗传背景的PD患者均显示出益处,但LRRK2突变携带者可能需要随时间增加刺激量,而GBA突变携带者的运动和生活质量改善较小。

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