Assessment of EEG dynamical complexity in Alzheimer's disease using multiscale entropy

被引:199
作者
Mizuno, Tomoyuki [1 ]
Takahashi, Tetsuya [1 ,2 ]
Cho, Raymond Y. [2 ]
Kikuchi, Mitsuru [3 ]
Murata, Tetsuhito [1 ]
Takahashi, Koichi [4 ]
Wada, Yuji [1 ]
机构
[1] Univ Fukui, Fac Med Sci, Dept Neuropsychiat, Eiheiji, Fukui 9101193, Japan
[2] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
[3] Kanazawa Univ, Grad Sch Med Sci, Dept Psychiat & Neurobiol, Kanazawa, Ishikawa, Japan
[4] Kinki Univ, Fac Sci & Engn, Dept Informat, Higashiosaka, Osaka 577, Japan
基金
日本学术振兴会;
关键词
Alzheimer's disease (AD); Electroencephalogram (EEG); Complexity; Multiscale entropy (MSE); Mini-Mental State Examination (MMSE); Power analysis; BACKGROUND ACTIVITY; INFORMATION; MEG;
D O I
10.1016/j.clinph.2010.03.025
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Multiscale entropy (MSE) is a recently proposed entropy-based index of physiological complexity, evaluating signals at multiple temporal scales. To test this method as an aid to elucidating the pathophysiology of Alzheimer's disease (AD), we examined MSE in resting state EEG activity in comparison with traditional EEG analysis. Methods: We recorded EEG in medication-free 15 presenile AD patients and 18 age-and sex-matched healthy control (HC) subjects. MSE was calculated for continuous 60-s epochs for each group, concurrently with power analysis. Results: The MSE results from smaller and larger scales were associated with higher and lower frequencies of relative power, respectively. Group analysis demonstrated that the AD group had less complexity at smaller scales in more frontal areas, consistent with previous findings. In contrast, higher complexity at larger scales was observed across brain areas in AD group and this higher complexity was significantly correlated with cognitive decline. Conclusions: MSE measures identified an abnormal complexity profile across different temporal scales and their relation to the severity of AD. Significance: These findings indicate that entropy-based analytic methods with applied at temporal scales may serve as a complementary approach for characterizing and understanding abnormal cortical dynamics in AD. (C) 2010 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1438 / 1446
页数:9
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