Sources of cortical rhythms change as a function of cognitive impairment in pathological aging: a multicenter study
The present study tested the hypothesis that cortical electroencephalographic (EEG) rhythms. change across normal elderly (Nold), mild cognitive impairment (MCI), and Alzheimer's disease (AD) subjects as a function of the global cognitive level. Resting eyes-closed EEG data were recorded in 155...
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Published in | Clinical neurophysiology Vol. 117; no. 2; pp. 252 - 268 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Shannon
Elsevier Ireland Ltd
01.02.2006
Elsevier Science |
Subjects | |
Online Access | Get full text |
ISSN | 1388-2457 1872-8952 |
DOI | 10.1016/j.clinph.2005.09.019 |
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Summary: | The present study tested the hypothesis that cortical electroencephalographic (EEG) rhythms. change across normal elderly (Nold), mild cognitive impairment (MCI), and Alzheimer's disease (AD) subjects as a function of the global cognitive level.
Resting eyes-closed EEG data were recorded in 155 MCI, 193 mild AD, and 126 age-matched Nold subjects. EEG rhythms of interest were delta (2–4
Hz), theta (4–8
Hz), alpha 1 (8–10.5
Hz), alpha 2 (10.5–13
Hz), beta 1 (13–20
Hz), and beta 2 (20–30
Hz). EEG cortical sources were estimated by LORETA.
Occipital delta and alpha 1 sources in parietal, occipital, temporal, and ‘limbic’ areas had an intermediate magnitude in MCI subjects compared to mild AD and Nold subjects. These five EEG sources presented both linear and nonlinear (linear, exponential, logarithmic, and power) correlations with the global cognitive level (as revealed by mini mental state examination score) across all subjects.
Cortical EEG rhythms change in pathological aging as a function of the global cognitive level.
The present functional data on large populations support the ‘transitional hypothesis’ of a shadow zone across normality, pre-clinical stage of dementia (MCI), and AD. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1388-2457 1872-8952 |
DOI: | 10.1016/j.clinph.2005.09.019 |