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Narrative Organization Deficit in Lewy Body Disorders Is Related to Alzheimer Pathology
Background: Day-to-day interactions depend on conversational narrative, and we examine here the neurobiological basis for difficulty organizing narrative discourse in patients with Lewy body disorders (LBD). Method: Narrative organization was examined in 56 non-aphasic LBD patients, including a non-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5296303/ https://www.ncbi.nlm.nih.gov/pubmed/28228714 http://dx.doi.org/10.3389/fnins.2017.00053 |
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author | Grossman, Murray Irwin, David J. Jester, Charles Halpin, Amy Ash, Sharon Rascovsky, Katya Weintraub, Daniel McMillan, Corey T. |
author_facet | Grossman, Murray Irwin, David J. Jester, Charles Halpin, Amy Ash, Sharon Rascovsky, Katya Weintraub, Daniel McMillan, Corey T. |
author_sort | Grossman, Murray |
collection | PubMed |
description | Background: Day-to-day interactions depend on conversational narrative, and we examine here the neurobiological basis for difficulty organizing narrative discourse in patients with Lewy body disorders (LBD). Method: Narrative organization was examined in 56 non-aphasic LBD patients, including a non-demented cohort (n = 30) with Parkinson's disease (PD) or PD-Mild Cognitive Impairment PD-MCI,) and a cohort with mild dementia (n = 26) including PD-dementia (PDD) and dementia with Lewy bodies (DLB), with similar age and education but differing in MMSE (p < 0.001). We used a previously reported procedure that probes patients' judgments of the organization of brief, familiar narratives (e.g., going fishing, wrapping a present). A subgroup of 24 patients had MRI assessment of regional gray matter (GM) atrophy and cerebrospinal fluid (CSF) levels of biomarkers for Alzheimer's disease (AD) pathology, including beta amyloid (Aβ), total-tau (t-tau), and phosphorylated-tau (p-tau). Results: Mildly demented LBD patients had a significant deficit judging narratives compared to non-demented patients, but this deficit was not correlated with MMSE. Regression analyses instead related narrative organization to regions of frontal GM atrophy, and CSF levels of Aβ and t-tau associated with presumed AD pathology in these frontal regions. Conclusion: These findings are consistent with the hypothesis that CSF markers of AD pathology associated with frontal regions play a role in difficulty organizing narratives in LBD. |
format | Online Article Text |
id | pubmed-5296303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52963032017-02-22 Narrative Organization Deficit in Lewy Body Disorders Is Related to Alzheimer Pathology Grossman, Murray Irwin, David J. Jester, Charles Halpin, Amy Ash, Sharon Rascovsky, Katya Weintraub, Daniel McMillan, Corey T. Front Neurosci Neuroscience Background: Day-to-day interactions depend on conversational narrative, and we examine here the neurobiological basis for difficulty organizing narrative discourse in patients with Lewy body disorders (LBD). Method: Narrative organization was examined in 56 non-aphasic LBD patients, including a non-demented cohort (n = 30) with Parkinson's disease (PD) or PD-Mild Cognitive Impairment PD-MCI,) and a cohort with mild dementia (n = 26) including PD-dementia (PDD) and dementia with Lewy bodies (DLB), with similar age and education but differing in MMSE (p < 0.001). We used a previously reported procedure that probes patients' judgments of the organization of brief, familiar narratives (e.g., going fishing, wrapping a present). A subgroup of 24 patients had MRI assessment of regional gray matter (GM) atrophy and cerebrospinal fluid (CSF) levels of biomarkers for Alzheimer's disease (AD) pathology, including beta amyloid (Aβ), total-tau (t-tau), and phosphorylated-tau (p-tau). Results: Mildly demented LBD patients had a significant deficit judging narratives compared to non-demented patients, but this deficit was not correlated with MMSE. Regression analyses instead related narrative organization to regions of frontal GM atrophy, and CSF levels of Aβ and t-tau associated with presumed AD pathology in these frontal regions. Conclusion: These findings are consistent with the hypothesis that CSF markers of AD pathology associated with frontal regions play a role in difficulty organizing narratives in LBD. Frontiers Media S.A. 2017-02-08 /pmc/articles/PMC5296303/ /pubmed/28228714 http://dx.doi.org/10.3389/fnins.2017.00053 Text en Copyright © 2017 Grossman, Irwin, Jester, Halpin, Ash, Rascovsky, Weintraub and McMillan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Grossman, Murray Irwin, David J. Jester, Charles Halpin, Amy Ash, Sharon Rascovsky, Katya Weintraub, Daniel McMillan, Corey T. Narrative Organization Deficit in Lewy Body Disorders Is Related to Alzheimer Pathology |
title | Narrative Organization Deficit in Lewy Body Disorders Is Related to Alzheimer Pathology |
title_full | Narrative Organization Deficit in Lewy Body Disorders Is Related to Alzheimer Pathology |
title_fullStr | Narrative Organization Deficit in Lewy Body Disorders Is Related to Alzheimer Pathology |
title_full_unstemmed | Narrative Organization Deficit in Lewy Body Disorders Is Related to Alzheimer Pathology |
title_short | Narrative Organization Deficit in Lewy Body Disorders Is Related to Alzheimer Pathology |
title_sort | narrative organization deficit in lewy body disorders is related to alzheimer pathology |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5296303/ https://www.ncbi.nlm.nih.gov/pubmed/28228714 http://dx.doi.org/10.3389/fnins.2017.00053 |
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