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Research article summary (published 25 Apr 2006):
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Absent event-related potential (ERP) word repetition effects in mild Alzheimer's disease.

Full Abstract

OBJECTIVE:
We hypothesized that an ERP word repetition paradigm, which reliably elicits and modulates the P600 and N400 components, would be particularly sensitive to the memory deficits and altered synaptic plasticity in mild Alzheimer's disease (AD). The P600 (a late positive component, or 'LPC'), and the N400, are sensitive indices of memory encoding and semantic processing, respectively.

METHODS:
We studied 11 patients with mild AD (mean MMSE=22.9) and 11 elderly (mean age=77.1) normal controls (NC) on a paradigm in which semantically 'congruous' category statement/exemplar pairs (50%) and 'incongruous' category statement/non-exemplar pairs (50%) repeat at 10-140 s intervals. A minimum of 19 channels ERP data were recorded and submitted to split-plot ANOVAs.

RESULTS:
Normal ERP data showed:
(1) a significant word repetition effect for congruous words, with a wide-spread late positivity between approximately 300 and 800 ms post-stimulus (P600) that is larger for New than Old words; (2) a significant N400 repetition effect for incongruous words, with a right posterior negativity that is reduced for Old relative to New words. By contrast, neither of these word repetition effects was reliably present in the mild AD group. Good group discrimination was achieved by requiring that both these repetition effects were > or = the 10th percentile, with 100% sensitivity and 82% specificity.

CONCLUSIONS:
We found significant abnormalities of the N400 and P600 in mild AD, with both potentials showing markedly reduced sensitivity to word repetition.

SIGNIFICANCE:
The absence of normal N400 and LPC/P600 word repetition effects suggests impaired functioning of their neural generators, several of which are located in medial temporal lobe predilection sites (e.g. anterior fusiform, parahippocampal gyrus, hippocampus) for AD/tau pathology.

 

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Author information

Author/s: Olichney, John M (JM); Iragui, Vicente J (VJ); Salmon, David P (DP); Riggins, Brock R (BR); Morris, Shaunna K (SK); Kutas, Marta (M);

Affiliation: Department of Neurosciences, University of California, San Diego, CA 92161, USA. olichney(-atsign-)cogsci.uscd.edu

Grants: P50 AG005131-22 (Agency:NIA NIH HHS) ; P50AG05131 (Agency:NIA NIH HHS) ; R01 AG008313-11A1 (Agency:NIA NIH HHS) ; R01 AG018442-05 (Agency:NIA NIH HHS) ; R01 AG08313 (Agency:NIA NIH HHS) ; R01 AG18442 (Agency:NIA NIH HHS)

Journal and publication information

Publication Type: Controlled Clinical Trial; Journal Article; Research Support, N.I.H., Extramural

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology (Clin Neurophysiol), published in Netherlands. (Language: eng)

Reference: 2006-Jun; vol 117 (issue 6) : pp 1319-30

Dates: Created 2006/06/12; Completed 2006/08/24; Revised 2008/11/20;

PMID: 16644278, 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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