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Serum levels of soluble TNF-α receptors but not BDNF are associated with apathy symptoms in mild Alzheimer's disease and amnestic mild cognitive impairment

Apathy is intimately associated with dementia. Unfortunately, its pathophysiology remains poorly understood. The motivational impairment that characterizes this disorder might share the same inflammatory mechanisms, as suggested by the sickness behavior theory. OBJECTIVE: The primary aim of this stu...

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Autores principales: Guimarães, Henrique Cerqueira, Caramelli, Paulo, Fialho, Patricia Paes Araujo, França, Elisa de Paula, Afonso, Marcelo Pelizzaro Dias, Teixeira, Antonio Lucio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Neurologia Cognitiva e do Comportamento 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619202/
https://www.ncbi.nlm.nih.gov/pubmed/29213854
http://dx.doi.org/10.1590/S1980-57642013DN70300011
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author Guimarães, Henrique Cerqueira
Caramelli, Paulo
Fialho, Patricia Paes Araujo
França, Elisa de Paula
Afonso, Marcelo Pelizzaro Dias
Teixeira, Antonio Lucio
author_facet Guimarães, Henrique Cerqueira
Caramelli, Paulo
Fialho, Patricia Paes Araujo
França, Elisa de Paula
Afonso, Marcelo Pelizzaro Dias
Teixeira, Antonio Lucio
author_sort Guimarães, Henrique Cerqueira
collection PubMed
description Apathy is intimately associated with dementia. Unfortunately, its pathophysiology remains poorly understood. The motivational impairment that characterizes this disorder might share the same inflammatory mechanisms, as suggested by the sickness behavior theory. OBJECTIVE: The primary aim of this study was to investigate the association between apathy symptoms and serum levels of tumor necrosis factor alpha (TNF-α) and its soluble receptors. Brain-derived neurotrophic factor (BDNF) levels were also analyzed since these have been associated with depression, a condition which shares abulic features with apathy. METHODS: The sample consisted of 27 subjects with mild Alzheimer's disease or amnestic mild cognitive impairment, who were submitted to specific apathy evaluation using the Apathy Scale (AS) and provided blood samples for biomarker analysis. Participants were categorized into two groups according to median AS scores (17 points). RESULTS: Subjects with higher apathy symptoms (n=13) displayed higher levels of TNF-α soluble receptors (type 1: p=0.03; type 2: p=0.04). No other difference was found between groups. CONCLUSION: These findings point to the involvement of inflammatory mediators in the genesis of apathy symptoms, as suggested by the sickness behavior theory.
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spelling pubmed-56192022017-12-06 Serum levels of soluble TNF-α receptors but not BDNF are associated with apathy symptoms in mild Alzheimer's disease and amnestic mild cognitive impairment Guimarães, Henrique Cerqueira Caramelli, Paulo Fialho, Patricia Paes Araujo França, Elisa de Paula Afonso, Marcelo Pelizzaro Dias Teixeira, Antonio Lucio Dement Neuropsychol Original Article Apathy is intimately associated with dementia. Unfortunately, its pathophysiology remains poorly understood. The motivational impairment that characterizes this disorder might share the same inflammatory mechanisms, as suggested by the sickness behavior theory. OBJECTIVE: The primary aim of this study was to investigate the association between apathy symptoms and serum levels of tumor necrosis factor alpha (TNF-α) and its soluble receptors. Brain-derived neurotrophic factor (BDNF) levels were also analyzed since these have been associated with depression, a condition which shares abulic features with apathy. METHODS: The sample consisted of 27 subjects with mild Alzheimer's disease or amnestic mild cognitive impairment, who were submitted to specific apathy evaluation using the Apathy Scale (AS) and provided blood samples for biomarker analysis. Participants were categorized into two groups according to median AS scores (17 points). RESULTS: Subjects with higher apathy symptoms (n=13) displayed higher levels of TNF-α soluble receptors (type 1: p=0.03; type 2: p=0.04). No other difference was found between groups. CONCLUSION: These findings point to the involvement of inflammatory mediators in the genesis of apathy symptoms, as suggested by the sickness behavior theory. Associação de Neurologia Cognitiva e do Comportamento 2013 /pmc/articles/PMC5619202/ /pubmed/29213854 http://dx.doi.org/10.1590/S1980-57642013DN70300011 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Guimarães, Henrique Cerqueira
Caramelli, Paulo
Fialho, Patricia Paes Araujo
França, Elisa de Paula
Afonso, Marcelo Pelizzaro Dias
Teixeira, Antonio Lucio
Serum levels of soluble TNF-α receptors but not BDNF are associated with apathy symptoms in mild Alzheimer's disease and amnestic mild cognitive impairment
title Serum levels of soluble TNF-α receptors but not BDNF are associated with apathy symptoms in mild Alzheimer's disease and amnestic mild cognitive impairment
title_full Serum levels of soluble TNF-α receptors but not BDNF are associated with apathy symptoms in mild Alzheimer's disease and amnestic mild cognitive impairment
title_fullStr Serum levels of soluble TNF-α receptors but not BDNF are associated with apathy symptoms in mild Alzheimer's disease and amnestic mild cognitive impairment
title_full_unstemmed Serum levels of soluble TNF-α receptors but not BDNF are associated with apathy symptoms in mild Alzheimer's disease and amnestic mild cognitive impairment
title_short Serum levels of soluble TNF-α receptors but not BDNF are associated with apathy symptoms in mild Alzheimer's disease and amnestic mild cognitive impairment
title_sort serum levels of soluble tnf-α receptors but not bdnf are associated with apathy symptoms in mild alzheimer's disease and amnestic mild cognitive impairment
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619202/
https://www.ncbi.nlm.nih.gov/pubmed/29213854
http://dx.doi.org/10.1590/S1980-57642013DN70300011
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