Butenko Konstantin, Neudorfer Clemens, Dembek Till A, Hollunder Barbara, Meyer Garance M, Li Ningfei, Oxenford Simón, Bahners Bahne H, Al-Fatly Bassam, Lofredi Roxanne, Gordon Evan M, Dosenbach Nico U F, Ganos Christos, Hallett Mark, Jinnah Hyder A, Starr Philip A, Ostrem Jill L, Wu Yiwen, Zhang ChenCheng, Fox Michael D, Horn Andreas
Center for Brain Circuit Therapeutics, Department of Neurology, Brigham & Women's Hospital, Harvard Medical School, Boston, MA 02115.
Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Proc Natl Acad Sci U S A. 2025 Jan 14;122(2):e2417617122. doi: 10.1073/pnas.2417617122. Epub 2025 Jan 8.
Deep brain stimulation is an efficacious treatment for dystonia. While the internal pallidum serves as the primary target, recently, stimulation of the subthalamic nucleus (STN) has been investigated. However, optimal targeting within this structure and its surroundings have not been studied in depth. Indeed, historical targets that have been used for surgical treatment of dystonia are directly adjacent to the STN. Further, multiple types of dystonia exist, and outcomes are variable, suggesting that not all types would profit maximally from the same target. Therefore, a thorough investigation of neural substrates underlying stimulation effects on dystonia signs and symptoms is warranted. Here, we analyze a multicenter cohort of isolated dystonia patients with subthalamic implantations ( = 58) and relate their stimulation sites to improvements of appendicular and cervical symptoms as well as blepharospasm. Stimulation of the ventral oral posterior nucleus of thalamus and surrounding regions were associated with improvements in cervical dystonia, while stimulation of the dorsolateral STN was associated with improvements in limb dystonia and blepharospasm. This dissociation was matched by structural connectivity analysis, where the cerebellothalamic, corticospinal, and pallidosubthalamic tracts were associated with improvements of cervical dystonia, while hyperdirect and subthalamopallidal pathways with alleviation of limb dystonia and blepharospasm. On the level of functional networks, improvements of limb dystonia were associated with connectivity to the corresponding somatotopic regions in the primary motor cortex, while alleviation of cervical dystonia to the cingulo-opercular network. These findings shed light on the pathophysiology of dystonia and may guide DBS targeting and programming in the future.
脑深部电刺激是治疗肌张力障碍的一种有效方法。虽然内侧苍白球是主要靶点,但最近,对丘脑底核(STN)的刺激也进行了研究。然而,该结构及其周围区域的最佳靶点尚未得到深入研究。事实上,用于肌张力障碍手术治疗的历史靶点直接毗邻STN。此外,存在多种类型的肌张力障碍,且治疗结果各不相同,这表明并非所有类型的肌张力障碍都能从同一靶点中获得最大益处。因此,有必要对刺激对肌张力障碍体征和症状的影响所涉及的神经基质进行全面研究。在此,我们分析了一组多中心的孤立性肌张力障碍患者队列(n = 58),这些患者接受了丘脑底核植入,并将他们的刺激部位与肢体和颈部症状以及眼睑痉挛的改善情况相关联。刺激丘脑腹后外侧核及其周围区域与颈部肌张力障碍的改善相关,而刺激STN的背外侧与肢体肌张力障碍和眼睑痉挛的改善相关。这种分离与结构连接性分析结果相匹配,其中小脑丘脑束、皮质脊髓束和苍白球丘脑底核束与颈部肌张力障碍的改善相关,而超直接通路和丘脑底核苍白球通路与肢体肌张力障碍和眼睑痉挛的缓解相关。在功能网络层面,肢体肌张力障碍的改善与与初级运动皮层中相应躯体感觉区域的连接性相关,而颈部肌张力障碍的缓解与扣带回-岛叶网络相关。这些发现揭示了肌张力障碍的病理生理学机制,并可能为未来的脑深部电刺激靶点选择和程控提供指导。