Sankar Tejas, Chakravarty M Mallar, Bescos Agustin, Lara Monica, Obuchi Toshiki, Laxton Adrian W, McAndrews Mary Pat, Tang-Wai David F, Workman Clifford I, Smith Gwenn S, Lozano Andres M
Division of Neurosurgery, University of Alberta, Edmonton, Alberta, Canada.
Cerebral Imaging Centre, Douglas Mental Health University Institute, Montreal, Quebec, Canada.
Brain Stimul. 2015 May-Jun;8(3):645-54. doi: 10.1016/j.brs.2014.11.020. Epub 2014 Dec 3.
Deep Brain Stimulation (DBS) is thought to improve the symptoms of selected neurological disorders by modulating activity within dysfunctional brain circuits. To date, there is no evidence that DBS counteracts progressive neurodegeneration in any particular disorder.
OBJECTIVE/HYPOTHESIS: We hypothesized that DBS applied to the fornix in patients with Alzheimer's Disease (AD) could have an effect on brain structure.
In six AD patients receiving fornix DBS, we used structural MRI to assess one-year change in hippocampal, fornix, and mammillary body volume. We also used deformation-based morphometry to identify whole-brain structural changes. We correlated volumetric changes to hippocampal glucose metabolism. We also compared volumetric changes to those in an age-, sex-, and severity-matched group of AD patients (n = 25) not receiving DBS.
We observed bilateral hippocampal volume increases in the two patients with the best clinical response to fornix DBS. In one patient, hippocampal volume was preserved three years after diagnosis. Overall, mean hippocampal atrophy was significantly slower in the DBS group compared to the matched AD group, and no matched AD patients demonstrated bilateral hippocampal enlargement. Across DBS patients, hippocampal volume change correlated strongly with hippocampal metabolism and with volume change in the fornix and mammillary bodies, suggesting a circuit-wide effect of stimulation. Deformation-based morphometry in DBS patients revealed local volume expansions in several regions typically atrophied in AD.
We present the first in-human evidence that, in addition to modulating neural circuit activity, DBS may influence the natural course of brain atrophy in a neurodegenerative disease.
深部脑刺激(DBS)被认为可通过调节功能失调的脑回路中的活动来改善某些神经系统疾病的症状。迄今为止,尚无证据表明DBS能对抗任何特定疾病中的进行性神经退行性变。
目的/假设:我们假设对阿尔茨海默病(AD)患者的穹窿进行DBS可能会对脑结构产生影响。
在6名接受穹窿DBS的AD患者中,我们使用结构MRI评估海马体、穹窿和乳头体体积在1年内的变化。我们还使用基于变形的形态测量法来识别全脑结构变化。我们将体积变化与海马体葡萄糖代谢进行关联。我们还将体积变化与未接受DBS的年龄、性别和严重程度匹配的AD患者组(n = 25)的变化进行比较。
我们观察到对穹窿DBS临床反应最佳的两名患者双侧海马体体积增加。在一名患者中,诊断三年后海马体体积得以保留。总体而言,与匹配的AD组相比,DBS组的平均海马体萎缩明显较慢,且没有匹配的AD患者出现双侧海马体增大。在所有接受DBS的患者中,海马体体积变化与海马体代谢以及穹窿和乳头体的体积变化密切相关,表明刺激具有全脑回路效应。对接受DBS的患者进行基于变形的形态测量法显示,AD中通常萎缩的几个区域出现局部体积扩张。
我们提供了首个在人体中的证据,表明除了调节神经回路活动外,DBS可能会影响神经退行性疾病中脑萎缩的自然进程。