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A unified brain system of orientation and its disruption in Alzheimer’s disease
OBJECTIVE: To investigate whether a unified brain system manages one’s orientation to different places, events and people in one’s environment, and test the hypothesis that failure of this system (disorientation) is an early sign of Alzheimer’s disease (AD). METHODS: A total of 46 participants (pati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917329/ https://www.ncbi.nlm.nih.gov/pubmed/31738022 http://dx.doi.org/10.1002/acn3.50940 |
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author | Dafni‐Merom, Amnon Peters‐Founshtein, Gregory Kahana‐Merhavi, Shlomzion Arzy, Shahar |
author_facet | Dafni‐Merom, Amnon Peters‐Founshtein, Gregory Kahana‐Merhavi, Shlomzion Arzy, Shahar |
author_sort | Dafni‐Merom, Amnon |
collection | PubMed |
description | OBJECTIVE: To investigate whether a unified brain system manages one’s orientation to different places, events and people in one’s environment, and test the hypothesis that failure of this system (disorientation) is an early sign of Alzheimer’s disease (AD). METHODS: A total of 46 participants (patients along the AD continuum and cognitively normal control subjects) were tested in a personalized, ecologically valid task of orientation relating to the participant’s own world in space, time and person under high–density electroencephalography. As a first step, we used evoked potential mapping to search for brain topography correlated with participants’ performance in orientating themselves to different places (space), events (time) and people (person) (Experiment 1). We then compared behavioral and electrophysiological changes in patients along the AD continuum (Experiment 2). RESULTS: We identified a specific brain topography (“orientation map”) that was active for orientation in space, time and person in correlation to participants’ performance. Both performance and the map’s strength gradually decreased from health to mild cognitive impairment (MCI) and from MCI to AD. Another map, immediately preceding the orientation map, showed the longest activity in patients with MCI, significantly more than both patients with AD and cognitively normal controls. INTERPRETATION: Our findings demonstrate that the same brain topography accounts for orientation in the different domains of space, time and person and provide a nexus between deterioration in patients’ orientation with the aggravation of Alzheimer’s disease. |
format | Online Article Text |
id | pubmed-6917329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69173292019-12-23 A unified brain system of orientation and its disruption in Alzheimer’s disease Dafni‐Merom, Amnon Peters‐Founshtein, Gregory Kahana‐Merhavi, Shlomzion Arzy, Shahar Ann Clin Transl Neurol Research Articles OBJECTIVE: To investigate whether a unified brain system manages one’s orientation to different places, events and people in one’s environment, and test the hypothesis that failure of this system (disorientation) is an early sign of Alzheimer’s disease (AD). METHODS: A total of 46 participants (patients along the AD continuum and cognitively normal control subjects) were tested in a personalized, ecologically valid task of orientation relating to the participant’s own world in space, time and person under high–density electroencephalography. As a first step, we used evoked potential mapping to search for brain topography correlated with participants’ performance in orientating themselves to different places (space), events (time) and people (person) (Experiment 1). We then compared behavioral and electrophysiological changes in patients along the AD continuum (Experiment 2). RESULTS: We identified a specific brain topography (“orientation map”) that was active for orientation in space, time and person in correlation to participants’ performance. Both performance and the map’s strength gradually decreased from health to mild cognitive impairment (MCI) and from MCI to AD. Another map, immediately preceding the orientation map, showed the longest activity in patients with MCI, significantly more than both patients with AD and cognitively normal controls. INTERPRETATION: Our findings demonstrate that the same brain topography accounts for orientation in the different domains of space, time and person and provide a nexus between deterioration in patients’ orientation with the aggravation of Alzheimer’s disease. John Wiley and Sons Inc. 2019-11-18 /pmc/articles/PMC6917329/ /pubmed/31738022 http://dx.doi.org/10.1002/acn3.50940 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Dafni‐Merom, Amnon Peters‐Founshtein, Gregory Kahana‐Merhavi, Shlomzion Arzy, Shahar A unified brain system of orientation and its disruption in Alzheimer’s disease |
title | A unified brain system of orientation and its disruption in Alzheimer’s disease |
title_full | A unified brain system of orientation and its disruption in Alzheimer’s disease |
title_fullStr | A unified brain system of orientation and its disruption in Alzheimer’s disease |
title_full_unstemmed | A unified brain system of orientation and its disruption in Alzheimer’s disease |
title_short | A unified brain system of orientation and its disruption in Alzheimer’s disease |
title_sort | unified brain system of orientation and its disruption in alzheimer’s disease |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917329/ https://www.ncbi.nlm.nih.gov/pubmed/31738022 http://dx.doi.org/10.1002/acn3.50940 |
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