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基于 EEG α3/α2 频率比分析丘脑和基底节灰质,揭示轻度认知障碍患者的特定变化。

Analysis of grey matter in thalamus and basal ganglia based on EEG α3/α2 frequency ratio reveals specific changes in subjects with mild cognitive impairment.

机构信息

IRCCSS Centro Giovanni di Dio Fatebenefratelli, Brescia, Italy.

出版信息

ASN Neuro. 2012 Dec 14;4(7):e00103. doi: 10.1042/AN20120058.

Abstract

GM (grey matter) changes of thalamus and basal ganglia have been demonstrated to be involved in AD (Alzheimer's disease). Moreover, the increase of a specific EEG (electroencephalogram) marker, α3/α2, have been associated with AD-converters subjects with MCI (mild cognitive impairment). To study the association of prognostic EEG markers with specific GM changes of thalamus and basal ganglia in subjects with MCI to detect biomarkers (morpho-physiological) early predictive of AD and non-AD dementia. Seventy-four adult subjects with MCI underwent EEG recording and high-resolution 3D MRI (three-dimensional magnetic resonance imaging). The α3/α2 ratio was computed for each subject. Three groups were obtained according to increasing tertile values of α3/α2 ratio. GM density differences between groups were investigated using a VBM (voxel-based morphometry) technique. Subjects with higher α3/α2 ratios when compared with subjects with lower and middle α3/α2 ratios showed minor atrophy in the ventral stream of basal ganglia (head of caudate nuclei and accumbens nuclei bilaterally) and of the pulvinar nuclei in the thalamus; The integrated analysis of EEG and morpho-structural markers could be useful in the comprehension of anatomo-physiological underpinning of the MCI entity.

摘要

GM(灰质)变化丘脑和基底节已被证明参与 AD(阿尔茨海默病)。此外,特定 EEG(脑电图)标志物 α3/α2 的增加与 AD 转化者 MCI(轻度认知障碍)有关。本研究旨在探讨 MCI 患者中预后 EEG 标志物与丘脑和基底节特定 GM 变化的相关性,以检测 AD 和非 AD 痴呆的早期预测生物标志物(形态生理学)。74 名成人 MCI 患者接受了 EEG 记录和高分辨率 3D MRI(三维磁共振成像)检查。计算每个受试者的 α3/α2 比值。根据 α3/α2 比值的递增三分位数,获得三组。使用 VBM(基于体素的形态测量学)技术研究组间 GM 密度差异。与低和中 α3/α2 比值的受试者相比,α3/α2 比值较高的受试者双侧基底节腹侧流(尾状核头部和伏隔核)和丘脑的苍白球显示出较小的萎缩;EEG 和形态结构标志物的综合分析可有助于理解 MCI 实体的解剖生理学基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e86/3522208/074cd2b6d867/an004e103f01.jpg

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