Division of Neurosurgery, University of Toronto, Toronto, Ontario, Canada.
Edmond J. Safra Program in Parkinson's Disease and Morton and Gloria Shulman Movement Disorders Centre, Toronto Western Hospital, Toronto, Ontario, Canada.
J Neurol Neurosurg Psychiatry. 2024 Jan 11;95(2):167-170. doi: 10.1136/jnnp-2022-330734.
The loss of the ability to swim following deep brain stimulation (DBS), although rare, poses a worrisome risk of drowning. It is unclear what anatomic substrate and neural circuitry underlie this phenomenon. We report a case of cervical dystonia with lost ability to swim and dance during active stimulation of globus pallidus internus. We investigated the anatomical underpinning of this phenomenon using unique functional and structural imaging analysis.
Tesla (3T) functional MRI (fMRI) of the patient was used during active DBS and compared with a cohort of four matched patients without this side effect. Structural connectivity mapping was used to identify brain network engagement by stimulation.
fMRI during stimulation revealed significant (P<0.0001) stimulation-evoked responses (DBS ON<OFF) in the supplementary motor area (SMA). Probabilistic tractography revealed that the patient's VTAs engaged streamlines projecting to SMA. Compared with a cohort of matched controls, the stimulation-dependent change in blood oxygen level-dependent response at the SMA was 2.18 SD below the mean.
These stimulation-induced impairments are likely a manifestation of a broader deficit in interlimb coordination mediated by stimulation effects on the SMA. This neuroanatomical underpinning can help inform future patient-specific stimulation and targeting.
尽管深部脑刺激(DBS)后丧失游泳能力很少见,但却存在令人担忧的溺水风险。目前尚不清楚是什么解剖基础和神经回路导致了这种现象。我们报告了一例苍白球 internus 内活动刺激后出现颈肌张力障碍和丧失游泳及跳舞能力的病例。我们使用独特的功能和结构成像分析来研究这种现象的解剖学基础。
在主动 DBS 期间对患者进行特斯拉(3T)功能磁共振成像(fMRI)检查,并与 4 名无此副作用的匹配患者进行比较。结构连接图用于识别刺激引起的大脑网络参与。
刺激期间的 fMRI 显示,辅助运动区(SMA)的刺激诱发反应(DBS ON<OFF)显著(P<0.0001)。概率轨迹显示,患者的 VTA 参与了投射到 SMA 的流线。与一组匹配的对照组相比,SMA 的血氧水平依赖反应的刺激依赖性变化比平均值低 2.18 个标准差。
这些由刺激引起的损伤可能是 SMA 刺激作用对四肢协调的更广泛缺陷的表现。这种神经解剖学基础可以帮助为未来的患者特异性刺激和靶向提供信息。