阿尔茨海默病脑电图伽马波段功率的评估。

IF 1.5 4区 心理学 Q4 CLINICAL NEUROLOGY
Vinurajkumar S, Yamuna Devi K, Manikandan K, Sathish S
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引用次数: 0

摘要

经颅交流电刺激(Gamma- tacs)用于治疗阿尔茨海默病(AD)。AD表现的脑电图(EEG)伽马波段功率(GBP)的变化可以证明通过γ - tacs增强GBP的可靠性。脑电图是由人类大脑的神经活动产生的电位。我们的目的是统计调查AD患者与健康受试者在额电极静息状态EEG的GBP差异有多大。该数据集包含65名参与者的脑电图记录,其中36名AD患者(66.39±7.89)岁,29名健康受试者(67.90±5.40)岁。Wilcoxon秩和检验显示,AD患者与健康者在额极1 (FP1) (p = 0.81)、FP2 (p = 0.48)、额3 (F3) (p = 0.77)、F7 (p = 0.76)、额区(Fz) (p = 0.65)、F4 (p = 0.91)、F8 (p = 0.42)的GBP差异不显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of Gamma Band Power of Electroencephalogram in Alzheimer's disease.

Gamma transcranial alternating current stimulation (Gamma-tACS) is used for treating Alzheimer's disease (AD). The changes in the Gamma band power (GBP) of Electroencephalogram (EEG) manifested by AD can justify the reliability of enhancing the GBP via the Gamma-tACS. The EEG is the electric potential originating from the neural activity of the human brain. Our objective is to statistically investigate how far the AD patients differ from the healthy subjects in terms of GBP of resting-state EEG at the frontal electrodes. The dataset contains EEG recordings from 65 participants comprising 36 AD patients with an age of 66.39 ± 7.89 and 29 healthy subjects with an age of 67.90 ± 5.40. As a major finding, the Wilcoxon rank-sum test reveals that the difference in GBP of AD patients and healthy subjects is not significant at frontal polar 1 (FP1) (p = 0.81), FP2 (p = 0.48), frontal 3 (F3) (p = 0.77), F7 (p = 0.76), frontal zone (Fz) (p = 0.65), F4 (p = 0.91), and F8 (p = 0.42).

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来源期刊
Applied Neuropsychology-Adult
Applied Neuropsychology-Adult CLINICAL NEUROLOGY-PSYCHOLOGY
CiteScore
4.50
自引率
11.80%
发文量
134
期刊介绍: pplied Neuropsychology-Adult publishes clinical neuropsychological articles concerning assessment, brain functioning and neuroimaging, neuropsychological treatment, and rehabilitation in adults. Full-length articles and brief communications are included. Case studies of adult patients carefully assessing the nature, course, or treatment of clinical neuropsychological dysfunctions in the context of scientific literature, are suitable. Review manuscripts addressing critical issues are encouraged. Preference is given to papers of clinical relevance to others in the field. All submitted manuscripts are subject to initial appraisal by the Editor-in-Chief, and, if found suitable for further considerations are peer reviewed by independent, anonymous expert referees. All peer review is single-blind and submission is online via ScholarOne Manuscripts.
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