CLC number: R741.044
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
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JIANG Zheng-yan. Abnormal cortical functional connections in Alzheimer’s disease: analysis of inter- and intra-hemispheric EEG coherence[J]. Journal of Zhejiang University Science B, 2005, 6(4): 259-264.
@article{title="Abnormal cortical functional connections in Alzheimer’s disease: analysis of inter- and intra-hemispheric EEG coherence",
author="JIANG Zheng-yan",
journal="Journal of Zhejiang University Science B",
volume="6",
number="4",
pages="259-264",
year="2005",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.2005.B0259"
}
%0 Journal Article
%T Abnormal cortical functional connections in Alzheimer’s disease: analysis of inter- and intra-hemispheric EEG coherence
%A JIANG Zheng-yan
%J Journal of Zhejiang University SCIENCE B
%V 6
%N 4
%P 259-264
%@ 1673-1581
%D 2005
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.2005.B0259
TY - JOUR
T1 - Abnormal cortical functional connections in Alzheimer’s disease: analysis of inter- and intra-hemispheric EEG coherence
A1 - JIANG Zheng-yan
J0 - Journal of Zhejiang University Science B
VL - 6
IS - 4
SP - 259
EP - 264
%@ 1673-1581
Y1 - 2005
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.2005.B0259
Abstract: To investigate inter- and intra-hemispheric electroencephalography (EEG) coherence at rest and during photic stimulation of patients with alzheimer’s disease (AD). Thirty-five patients (12 males, 23 females; 52~64 y) and 33 sex- and age-matched controls (12 males, 21 females; 56~65 y) were recruited in the present study. EEG signals from C3-C4, P3-P4, T5-T6 and O1-O2 electrode pairs resulted from the inter-hemispheric action, and EEG signals from C3-P3, C4-P4, P3-O1, P4-O2, C3-O1, C4-O2, T5-O1 and T6-O2 electrode pairs resulted from the intra-hemispheric action. The influence of inter- and intra-hemispheric coherence on EEG activity with eyes closed was examined, using fast Fourier transformation from the 16 sampled channels. The frequencies of photic stimulation were fixed at 5, 10 and 15 Hz, respectively. The general decrease of AD patients in inter- and intra-hemispheric EEG coherence was more significant than that of the normal controls at the resting EEG, with most striking decrease observed in the alpha-1 (8.0-9.0 Hz) and alpha-2 (9.5-12.5 Hz) bands. During photic stimulation, inter- and intra-hemispheric EEG coherences of the AD patients having lower values in the alpha (9.5-10.5 Hz) band than those of the control group. It suggests that under stimulated and non-stimulated conditions, AD patients had impaired inter- and intra-hemispheric functional connections, indicating failure of brain activation in alpha-related frequency.
[1] Basar, E., Yordanova, J., Kolev, V., Basar-Eroglu, C., 1997. Is the alpha rhythm a control parameter for brain responses? Boil Cybern, 76:471-480.
[2] Beaumont, J.G., Mayes, A.R., Rugg, M.D., 1978. Asymmetry in EEG alpha coherence and power: effects of task and sex. Electroencephalogy Clin. Neurophysiol, 45:393-401.
[3] Hogan, M.J., Swanwick, G.R.J., Kaiser, J., Rowan, M., Lawlor, B., 2003. Memory-related EEG power and coherence reduction in mild Alzheimer’s disease. Int. J. Psychophysiol, 49:147-163.
[4] Jiang, Z.Y., 2002. A study of EEG Photic driving in schizophrenia. Chinese Journal of Nervous and Mental Disease, 28(3):198-200 (in Chinese).
[5] Jiang, Z.Y., 2004. The research of diagnosis of Alzheimer’s disease based on the coherence analysis of EEG signal. Chinese Journal of Sensor and Actuator, 17(3):363-366 (in Chinese).
[6] Kikuchi, M., Wada, Y., Koshino, Y., Nanbu, Y., Hashino, T., 2000. Effects of scopolamine on inter-hemispheric EEG coherence in healthy subjects: analysis during rest and photic stimulation. Electroencephalogr. Clin. Neurophysiol, 31:109-115.
[7] Koeda, T., Knyazeva, M., Njiokiktjien, C., Jonkman, E.J., De Sonneville, L., Vildavsky, V., 1995. The EEG in acallosal children. Coherence values in the resting state: left hemisphere compensatory mechanism? Electroencephalogr Clin Neurophysiol, 95:397-407.
[8] Politoff, A.L., Monson, N., Hass, P., Stadter, R., 1992. Decreased alpha bandwidth responsiveness to photic driving in Alzheimer disease. Electroencephalogr Clin Neurophysiol, 82:45-52.
[9] Schurmann, M., Basar, E., 2001. Functional aspects of alpha oscillations in the EEG. Int. J. Psychophysiol., 39:151-158.
[10] Sloan, E.P., Fenton, G.W., Standage, K.P., 1992. Anticholinergic drug effects on quantitative electroencephalogram, visualevoked potential, and verbal memory. Biol. Psychiatry, 31:600-606.
[11] Tucker, D.M., Roth, D.L., Bair, T.B., 1986. Function connections among cortical regions: topography of EEG coherence. Electroencephalogr. Clin. Neurophysiol, 63:242-250.
[12] Vermersch, P., Scheltens, P., Barkhof, F., Steinling, M., Leys, D., 1994. Evidence for atrophy of the corpus callosum in Alzheimer’s disease. Eur. Neurol, 34(2):83-86.
[13] Wada, Y., Nanbu, Y., Jiang, Z.Y., Koshino, Y., Yamaguchi, N., Hashimoto, T., 1997. Electroencephalographic abnormalities in patients with presenile dementia of the Alzheimer type: quantitative analysis at rest and during photic stimulation. Biol. Psychiatry, 41:217-225.
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