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| Research article summary (published 13 Apr 2007): |
Memory activation reveals abnormal EEG in preclinical Huntington's disease.
Full Abstract
The EEG is potentially useful as a marker of early Huntington's disease (HD). In dementia, the EEG during a memory activation challenge showed abnormalities where the resting EEG did not. We investigated whether memory activation also reveals EEG abnormalities in preclinical HD. Sixteen mutation carriers for HD and 13 nonmutation carriers underwent neurological, neuropsychological, MRI and EEG investigations. The EEG was registered during a rest condition, i.e. eyes closed, and a working memory task. In each condition we determined absolute power in the theta (4-8 Hz) and alpha (8-13 Hz) bands and subsequently calculated relative alpha power. The EEG during eyes closed did not differ between groups. The EEG during memory activation showed less relative alpha power in mutation carriers as compared to nonmutation carriers, even though memory performance was similar [F (1,27) = 10.87; P = 0.003]. Absolute powers also showed less alpha power [F (1,27) = 7.02; P = 0.013] but similar theta power. No correlations were found between absolute and relative alpha power on the one hand and neuropsychological scores, motor scores or number of CAG repeats on the other. In conclusion, memory activation reveals functional brain changes in Huntington's disease before clinical signs become overt.
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Author information
Author/s: van der Hiele, Karin (K); Jurgens, Caroline K (CK); Vein, Alla A (AA); Reijntjes, Robert H A M (RH); Witjes-Ané, Marie-Noëlle W (MN); Roos, Raymund A C (RA); van Dijk, Gert (G); Middelkoop, Huub A M (HA);
Affiliation: Section of Neuropsychology, Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands. k.van_der_hiele(-atsign-)lumc.nl
Journal and publication information
Publication Type: Journal Article
Journal: Movement disorders : official journal of the Movement Disorder Society (Mov Disord), published in United States. (Language: eng)
Reference: 2007-Apr; vol 22 (issue 5) : pp 690-5
Dates: Created 2007/05/01; Completed 2007/07/23;
PMID: 17266047, status: MEDLINE (last retrieval date: 12/26/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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