带有 E280A Presenilin-1 突变基因的家族性阿尔茨海默病的脑电图频谱分析

Q1 Neuroscience International Journal of Alzheimer's Disease Pub Date : 2014-01-01 Epub Date: 2014-01-02 DOI:10.1155/2014/180741
Rene Rodriguez, Francisco Lopera, Alfredo Alvarez, Yuriem Fernandez, Lidice Galan, Yakeel Quiroz, Maria Antonieta Bobes
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摘要

目的:评估定量脑电图(qEEG)分析是否能检测家族性阿尔茨海默病(AD)临床前期的早期功能变化。研究人员从五个遗传性阿尔茨海默病大家庭中选取了三组受试者:可能患有阿尔茨海默病组(18 名受试者)、无症状携带者组(21 名受试者)(携带基因突变但无任何痴呆临床症状)和正常组(18 名健康受试者)。为了揭示频谱参数的显著差异,计算了组间的马哈拉诺比距离(D (2))。为了评估该统计量 D (2) 的诊断效率,使用了 ROC 模型。ROC 曲线通过准确度指数和标准偏差进行总结。使用快速频带能量参数计算的 D (2) 显示,正常组和 ACr 组之间(区域 ROC = 0.89)以及可能有注意力缺失症组和 ACr 组之间(区域 ROC = 0.91)有准确的区分。这在颞区更为明显。这些参数可能在发病前就受到影响,即使认知障碍在临床上并不明显。频谱脑电图参数可首先用于评估E280A Presenilin-1突变但认知功能未受损的受试者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Spectral Analysis of EEG in Familial Alzheimer's Disease with E280A Presenilin-1 Mutation Gene.

To evaluate the hypothesis that quantitative EEG (qEEG) analysis is susceptible to detect early functional changes in familial Alzheimer's disease (AD) preclinical stages. Three groups of subjects were selected from five extended families with hereditary AD: a Probable AD group (18 subjects), an asymptomatic carrier (ACr) group (21 subjects), with the mutation but without any clinical symptoms of dementia, and a normal group of 18 healthy subjects. In order to reveal significant differences in the spectral parameter, the Mahalanobis distance (D (2)) was calculated between groups. To evaluate the diagnostic efficiency of this statistic D (2), the ROC models were used. The ROC curve was summarized by accuracy index and standard deviation. The D (2) using the parameters of the energy in the fast frequency bands shows accurate discrimination between normal and ACr groups (area ROC = 0.89) and between AD probable and ACr groups (area ROC = 0.91). This is more significant in temporal regions. Theses parameters could be affected before the onset of the disease, even when cognitive disturbance is not clinically evident. Spectral EEG parameter could be firstly used to evaluate subjects with E280A Presenilin-1 mutation without impairment in cognitive function.

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来源期刊
International Journal of Alzheimer's Disease
International Journal of Alzheimer's Disease Neuroscience-Behavioral Neuroscience
CiteScore
10.10
自引率
0.00%
发文量
3
审稿时长
11 weeks
期刊最新文献
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