Altered generation of spontaneous oscillations in Alzheimer's disease

被引:101
|
作者
Osipova, D
Ahveninen, J
Jensen, O
Ylikoski, A
Pekkonen, E
机构
[1] Univ Helsinki, Cognit Brain Res Unit, Dept Psychol, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Cent Hosp, Ctr Engn, BioMag Lab, FIN-00014 Helsinki, Finland
[3] Helsinki Brain Res Ctr, Helsinki, Finland
[4] Harvard Univ, MIT, Massachusetts Gen Hosp, Sch Med,Athinoula A Martinos Ctr Biomed Imaging, Charlestown, MA 02129 USA
[5] FC Donders Ctr Cognit Neuroimaging, Nijmegen, Netherlands
[6] Hosp Koskela, Helsinki, Finland
[7] Univ Helsinki, Cent Hosp, Dept Neurol, FIN-00014 Helsinki, Finland
关键词
Alzheimer's disease; EEG; MEG; alpha activity; oscillatory sources;
D O I
10.1016/j.neuroimage.2005.05.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Slowing of spontaneous alpha oscillations and an anterior shift of a source of alpha activity (8-13 Hz) have been consistently reported in the EEG studies of Alzheimer's disease (AD). It is unknown whether these changes are associated with a gradual shift in location and frequency of existing sources or rather with the involvement of a new set of oscillators. We addressed this question by applying source modeling (minimum current estimates, NICE) to spontaneous alpha activity recorded with a 306-channel MEG system from eleven non-medicated AD patients with mild to moderate cognitive impairment and twelve age-matched controls during the eyes-closed session. AD patients had predominant lower alpha band sources in the temporal regions, whereas in the controls, robust alpha sources were found near the parieto-occipital sulcus. Activation within the parieto-occipital region was significantly weaker, and activation in the right temporal area was significantly enhanced in the AD patients. These results suggest an increased temporal-lobe contribution coinciding with parieto-occipital deficits. We propose that NICE, which provides simultaneous mapping of several oscillatory sources, might be useful for detecting neurophysiological abnormalities associated with AD in combination with other neuropsychological and neurological measures. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:835 / 841
页数:7
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