Strigaro Gionata, Gori Benedetta, Zoccola Clara, Vinassa Alessandro, Cattaneo Federica, Avino Gianluca, Barbero Paolo, Varrasi Claudia, Cantello Roberto
Neurology Unit, Department of Translational Medicine, University of Piemonte Orientale, and Azienda Ospedaliero-Universitaria "Maggiore della Carità", Novara, Italy.
Clin EEG Neurosci. 2024 May;55(3):347-353. doi: 10.1177/15500594221136856. Epub 2022 Nov 3.
.The pathophysiology of amnestic mild cognitive impairment (aMCI) and Alzheimer disease (AD) is still a matter of debate. Visual system might be precociously altered, especially for its cholinergic connections. We thus studied patients with aMCI compared to AD with paired-pulse flash-visual evoked potentials (paired-F-VEPs), a putative marker of cholinergic function. We enrolled 12 adult patients with aMCI and 12 with AD. 14 normal age- and sex-matched subjects acted as controls (HS). Stimuli were single flashes, with interspersed random flash pairs at critical interstimulus intervals (ISIs, 16.5 to 125 ms) with closed eyes. The "single" (unconditioned) F-VEP was split into a "main complex" (50 to 200 ms after the flash) and a "late response" (200 to 400 ms). As for paired stimulation, the "test" F-VEP emerged from electronic subtraction of the "single" F-VEP from the "paired"-F-VEP. In the single F-VEP, P2 latency was prolonged in patients (aMCI and AD) compared to HS ( < .05). As to the paired F-VEPs, in aMCI the "late response" normal inhibition was abolished at ISIs 50-62.5 ms ( ≤ .016), compared to AD and controls. No changes were detected for the "main complex". Paired-F-VEPs demonstrate a defective neural inhibition in the visual system of patients with aMCI at critical intervals. It may represent a compensatory mechanism against neuronal loss, the failure of which may be involved in AD development. Paired-F-VEPs may warrant inclusion in future preclinical/clinical studies, to evaluate its potential role in the pathophysiology and management of aMCI.
遗忘型轻度认知障碍(aMCI)和阿尔茨海默病(AD)的病理生理学仍是一个有争议的问题。视觉系统可能会过早改变,尤其是其胆碱能连接。因此,我们使用配对脉冲闪光视觉诱发电位(paired-F-VEPs,一种胆碱能功能的假定标志物)对aMCI患者与AD患者进行了研究。我们招募了12名成年aMCI患者和12名AD患者。14名年龄和性别匹配的正常受试者作为对照(HS)。刺激为单闪光,闭眼时在关键刺激间隔(ISI,16.5至125毫秒)穿插随机闪光对。“单”(非条件)F-VEP被分为“主复合体”(闪光后50至200毫秒)和“晚期反应”(200至400毫秒)。对于配对刺激,“测试”F-VEP通过从“配对”-F-VEP中电子减去“单”F-VEP得出。在单F-VEP中,与HS相比,患者(aMCI和AD)的P2潜伏期延长(<0.05)。对于配对F-VEPs,与AD和对照组相比,在aMCI中,ISI为50 - 62.5毫秒时“晚期反应”的正常抑制被消除(≤0.016)。“主复合体”未检测到变化。配对F-VEPs表明aMCI患者视觉系统在关键间隔存在神经抑制缺陷。它可能代表一种针对神经元丢失的代偿机制,其失效可能参与AD的发展。配对F-VEPs可能值得纳入未来的临床前/临床研究,以评估其在aMCI病理生理学和管理中的潜在作用。