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Decision-Making Deficits Associated with Amyloidosis in Lewy Body Disorders
Background: Lewy body disorders (LBD) are clinical syndromes characterized by pathological inclusions containing α-synuclein. Cognitive deficits are common or diagnostic in LBD, and may be associated with the presence of beta-amyloid (Aβ), which is a hallmark histopathologic abnormality characterist...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225123/ https://www.ncbi.nlm.nih.gov/pubmed/28123364 http://dx.doi.org/10.3389/fnhum.2016.00693 |
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author | Spotorno, Nicola McMillan, Corey T. Irwin, David J. Clark, Robin Lee, Edward B. Trojanowski, John Q. Weintraub, Daniel Grossman, Murray |
author_facet | Spotorno, Nicola McMillan, Corey T. Irwin, David J. Clark, Robin Lee, Edward B. Trojanowski, John Q. Weintraub, Daniel Grossman, Murray |
author_sort | Spotorno, Nicola |
collection | PubMed |
description | Background: Lewy body disorders (LBD) are clinical syndromes characterized by pathological inclusions containing α-synuclein. Cognitive deficits are common or diagnostic in LBD, and may be associated with the presence of beta-amyloid (Aβ), which is a hallmark histopathologic abnormality characteristic of Alzheimer's disease (AD) that can also co-occur with LBD. Objective: In the present study we evaluated whether social decision-making difficulties in LBD are associated with Aβ burden. Methods: Decision-making abilities were measured with a simple, untimed, behavioral task previously validated in patients with behavioral variant frontotemporal dementia, and performance was related to gray matter atrophy on MRI. Aβ burden was assessed by examination of cerebrospinal fluid (CSF) level of Aβ(1−42) and by autopsy confirmation in a subgroup of patients. Results: The results revealed that LBD patients with evidence of Aβ have reduced social decision-making abilities compared to patients with no evidence of Aβ. The imaging analysis related greater decision-making difficulty in Aβ-positive patients in respect to Aβ-negative patients to gray matter atrophy in medial orbitofrontal. This region is a critical node of a decision-making network as well as a region previously associated with comorbid α-synuclein and Aβ in LBD. Conclusions: These preliminary findings suggest that cognitive difficulties in LBD extend to include deficits in social decision-making and that this may be related to the presence of Aβ. |
format | Online Article Text |
id | pubmed-5225123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52251232017-01-25 Decision-Making Deficits Associated with Amyloidosis in Lewy Body Disorders Spotorno, Nicola McMillan, Corey T. Irwin, David J. Clark, Robin Lee, Edward B. Trojanowski, John Q. Weintraub, Daniel Grossman, Murray Front Hum Neurosci Neuroscience Background: Lewy body disorders (LBD) are clinical syndromes characterized by pathological inclusions containing α-synuclein. Cognitive deficits are common or diagnostic in LBD, and may be associated with the presence of beta-amyloid (Aβ), which is a hallmark histopathologic abnormality characteristic of Alzheimer's disease (AD) that can also co-occur with LBD. Objective: In the present study we evaluated whether social decision-making difficulties in LBD are associated with Aβ burden. Methods: Decision-making abilities were measured with a simple, untimed, behavioral task previously validated in patients with behavioral variant frontotemporal dementia, and performance was related to gray matter atrophy on MRI. Aβ burden was assessed by examination of cerebrospinal fluid (CSF) level of Aβ(1−42) and by autopsy confirmation in a subgroup of patients. Results: The results revealed that LBD patients with evidence of Aβ have reduced social decision-making abilities compared to patients with no evidence of Aβ. The imaging analysis related greater decision-making difficulty in Aβ-positive patients in respect to Aβ-negative patients to gray matter atrophy in medial orbitofrontal. This region is a critical node of a decision-making network as well as a region previously associated with comorbid α-synuclein and Aβ in LBD. Conclusions: These preliminary findings suggest that cognitive difficulties in LBD extend to include deficits in social decision-making and that this may be related to the presence of Aβ. Frontiers Media S.A. 2017-01-11 /pmc/articles/PMC5225123/ /pubmed/28123364 http://dx.doi.org/10.3389/fnhum.2016.00693 Text en Copyright © 2017 Spotorno, McMillan, Irwin, Clark, Lee, Trojanowski, Weintraub and Grossman. 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 Spotorno, Nicola McMillan, Corey T. Irwin, David J. Clark, Robin Lee, Edward B. Trojanowski, John Q. Weintraub, Daniel Grossman, Murray Decision-Making Deficits Associated with Amyloidosis in Lewy Body Disorders |
title | Decision-Making Deficits Associated with Amyloidosis in Lewy Body Disorders |
title_full | Decision-Making Deficits Associated with Amyloidosis in Lewy Body Disorders |
title_fullStr | Decision-Making Deficits Associated with Amyloidosis in Lewy Body Disorders |
title_full_unstemmed | Decision-Making Deficits Associated with Amyloidosis in Lewy Body Disorders |
title_short | Decision-Making Deficits Associated with Amyloidosis in Lewy Body Disorders |
title_sort | decision-making deficits associated with amyloidosis in lewy body disorders |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225123/ https://www.ncbi.nlm.nih.gov/pubmed/28123364 http://dx.doi.org/10.3389/fnhum.2016.00693 |
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