失忆性轻度认知障碍患者的视觉抑制能力受损

IF 1.6 4区 医学 Q3 CLINICAL NEUROLOGY Clinical EEG and Neuroscience Pub Date : 2024-05-01 Epub Date: 2022-11-03 DOI:10.1177/15500594221136856
Gionata Strigaro, Benedetta Gori, Clara Zoccola, Alessandro Vinassa, Federica Cattaneo, Gianluca Avino, Paolo Barbero, Claudia Varrasi, Roberto Cantello
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引用次数: 0

摘要

目的:关于失忆性轻度认知障碍(aMCI)和阿尔茨海默病(AD)的病理生理学仍存在争议。视觉系统可能提前发生改变,尤其是其胆碱能连接。因此,我们利用成对脉冲闪光视觉诱发电位(paired-pulse flash-visual evoked potentials,Paired-F-VEPs)--一种胆碱能功能的假定标志物--研究了轻度认知功能障碍(amnestic mild cognitive impairment,MCI)和阿尔茨海默病(Alzheimer disease,AD)患者。研究方法我们招募了 12 名 aMCI 和 12 名 AD 成年患者。14名年龄和性别匹配的正常人作为对照组(HS)。刺激物为单个闪光,并在闭眼状态下以临界刺激间隔(ISI,16.5 至 125 毫秒)穿插随机闪光对。单次"(无条件)F-VEP 被分为 "主复合"(闪光后 50 至 200 毫秒)和 "晚期反应"(200 至 400 毫秒)。至于配对刺激,"测试 "F-VEP 是通过电子方式从 "配对 "F-VEP 中减去 "单一 "F-VEP 而得出的。结果。在单一 F-VEP 中,与 HS 相比,患者(aMCI 和 AD)的 P2 潜伏期延长(p p ≤ .016),与 AD 和对照组相比也是如此。主复合体 "未发现任何变化。结论成对的F-VEPs显示,aMCI患者的视觉系统在关键时间间隔内存在神经抑制缺陷。这可能是对神经元缺失的一种补偿机制,这种机制的失效可能与注意力缺失症的发展有关。成对 F-VEPs 可能值得纳入未来的临床前/临床研究,以评估其在 aMCI 的病理生理学和治疗中的潜在作用。
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Impaired Visual Inhibition in Amnestic Mild Cognitive Impairment.

Objective.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. Methods. 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. Results. In the single F-VEP, P2 latency was prolonged in patients (aMCI and AD) compared to HS (p < .05). As to the paired F-VEPs, in aMCI the "late response" normal inhibition was abolished at ISIs 50-62.5 ms (p ≤ .016), compared to AD and controls. No changes were detected for the "main complex". Conclusions. 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.

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来源期刊
Clinical EEG and Neuroscience
Clinical EEG and Neuroscience 医学-临床神经学
CiteScore
5.20
自引率
5.00%
发文量
66
审稿时长
>12 weeks
期刊介绍: Clinical EEG and Neuroscience conveys clinically relevant research and development in electroencephalography and neuroscience. Original articles on any aspect of clinical neurophysiology or related work in allied fields are invited for publication.
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