Dorsolateral prefrontal cortex excitability abnormalities in Alzheimer's Dementia: Findings from transcranial magnetic stimulation and electroencephalography study

磁刺激 背外侧前额叶皮质 心理学 听力学 痴呆 脑电图 神经科学 前额叶皮质 认知 执行职能 刺激(心理学) 神经心理学 蒙特利尔认知评估 刺激 医学 内科学 认知障碍 认知心理学 疾病
作者
Shaylyn Joseph,Dunja Knezevic,Reza Zomorrodi,Daniel M. Blumberger,Zafiris J. Daskalakis,Benoit H. Mulsant,Bruce G. Pollock,Aristotle N. Voineskos,Wei Wang,Tarek K. Rajji,Sanjeev Kumar
出处
期刊:International Journal of Psychophysiology [Elsevier BV]
卷期号:169: 55-62 被引量:38
标识
DOI:10.1016/j.ijpsycho.2021.08.008
摘要

There is some evidence of cortical hyper-excitability in Alzheimer's Dementia (AD) but its relationship with cognition is not clear. In this study, we assessed dorsolateral prefrontal cortex (DLPFC) excitability and its relationship with cognition in AD. Twenty-four participants with AD (mean [SD] age = 74.1 [7.2] years) and eleven elderly healthy controls (HC) (mean [SD] age = 68.8 [7.3] years) were recruited. Transcranial magnetic stimulation (TMS) combined with electroencephalography (EEG) was used to assess cortical excitability. Cortical evoked activity (CEA) between 25 and 80 ms post-TMS stimulus was calculated as the primary measure of cortical excitability. TMS-evoked potential peak (TEP) amplitudes (P30, N45 and P60) were also calculated. Cognition was assessed using Montreal Cognitive Assessment (MoCA), Executive Interview (EXIT) and Cambridge Neuropsychological Test Automated Battery Stockings of Cambridge (SOC). There was no difference in TMS stimulus intensity between the groups. DLPFC-CEA was higher in the AD (mean [SD] = 134.64 [90.22] μV) than the HC group (mean [SD] = 82.65 [40.28] μV; t33 = 2.357, p = 0.025). There were no differences in TEP peak amplitudes between the groups. Further, DLPFC-CEA was inversely associated with MoCA and SOC, and positively associated with EXIT scores in AD. These results suggest increased DLPFC excitability in AD, and its inverse associations with global cognition and executive function. Future studies should examine these findings in larger samples and longitudinally, and could also assess these markers of cortical excitability in relation to other established markers of AD and in response to interventions.
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