Gordon Center for Medical Imaging, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Berenson-Allen Center for Noninvasive Brain Stimulation, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
J Alzheimers Dis. 2022;85(4):1667-1676. doi: 10.3233/JAD-215072.
Alzheimer's disease (AD) is characterized by diffuse amyloid-β (Aβ) and phosphorylated Tau (p-Tau) aggregates as well as neuroinflammation. Exogenously-induced 40 Hz gamma oscillations have been showing to reduce Aβ and p-Tau deposition presumably via microglia activation in AD mouse models.
We aimed to translate preclinical data on gamma-induction in AD patients by means of transcranial alternating current stimulation (tACS).
Four participants with mild-to-moderate AD received 1 h of daily 40 Hz (gamma) tACS for 4 weeks (Monday to Friday) targeting the bitemporal lobes (20 h treatment duration). Participant underwent Aβ, p-Tau, and microglia PET imaging with [11C]-PiB, [18F]-FTP, and [11C]-PBR28 respectively, before and after the intervention along with electrophysiological assessment.
No adverse events were reported, and an increase in gamma spectral power on EEG was observed after the treatment. [18F]-FTP PET revealed a significant decrease over 2% of p-Tau burden in 3/4 patients following the tACS treatment, primarily involving the temporal lobe regions targeted by tACS and especially mesial regions (e.g., entorhinal cortex). The amount of intracerebral Aβ as measured by [11C]-PiB was not significantly influenced by tACS, whereas 1/4 reported a significant decrease of microglia activation as measured by [11C]-PBR28.
tACS seems to represent a safe and feasible option for gamma induction in AD patients, with preliminary evidence of a possible effect on protein clearance partially mimicking what is observed in animal models. Longer interventions and placebo control conditions are needed to fully evaluate the potential for tACS to slow disease progression.
阿尔茨海默病(AD)的特征是弥漫性淀粉样β(Aβ)和磷酸化 Tau(p-Tau)聚集体以及神经炎症。在 AD 小鼠模型中,外源性诱导的 40Hz 伽马振荡已被证明可以通过小胶质细胞激活来减少 Aβ和 p-Tau 沉积。
我们旨在通过经颅交流电刺激(tACS)将 AD 患者伽马诱导的临床前数据转化为临床应用。
4 名轻度至中度 AD 患者接受了为期 4 周(周一至周五)、每天 1 小时的 40Hz(伽马)tACS 治疗(20 小时治疗时间),靶向双侧颞叶(20 小时治疗时间)。在干预前后,患者分别接受了 [11C]-PiB、[18F]-FTP 和 [11C]-PBR28 的 Aβ、p-Tau 和小胶质细胞 PET 成像,以及电生理评估。
未报告不良事件,并且在治疗后观察到 EEG 上的伽马光谱功率增加。[18F]-FTP PET 显示,在接受 tACS 治疗后,3/4 名患者的 p-Tau 负担下降了 2%以上,主要涉及 tACS 靶向的颞叶区域,特别是内侧区域(例如,内嗅皮层)。[11C]-PiB 测量的脑内 Aβ量不受 tACS 的显著影响,而 1/4 名患者报告说,[11C]-PBR28 测量的小胶质细胞激活显著减少。
tACS 似乎是 AD 患者诱导伽马的一种安全且可行的选择,初步证据表明其对蛋白清除可能有一定影响,部分类似于动物模型中的观察结果。需要更长时间的干预和安慰剂对照条件来全面评估 tACS 减缓疾病进展的潜力。