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Executive deficits detected in mild Alzheimer's disease using the antisaccade task

The antisaccade task, a hands- and language-free metric, may provide a functional index of the dorsolateral prefrontal cortex (DLPFC), a region damaged in the later stages of Alzheimer's disease (AD). Our objective was to determine if patients with mild AD made more errors relative to age-match...

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Detalles Bibliográficos
Autores principales: Kaufman, Liam D, Pratt, Jay, Levine, Brian, Black, Sandra E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Inc 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343295/
https://www.ncbi.nlm.nih.gov/pubmed/22574270
http://dx.doi.org/10.1002/brb3.28
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author Kaufman, Liam D
Pratt, Jay
Levine, Brian
Black, Sandra E
author_facet Kaufman, Liam D
Pratt, Jay
Levine, Brian
Black, Sandra E
author_sort Kaufman, Liam D
collection PubMed
description The antisaccade task, a hands- and language-free metric, may provide a functional index of the dorsolateral prefrontal cortex (DLPFC), a region damaged in the later stages of Alzheimer's disease (AD). Our objective was to determine if patients with mild AD made more errors relative to age-matched controls. Thirty patients with mild AD (Mini Mental Status Exam [MMSE] ≥ 17) and 31 age-matched controls completed a laptop version of the prosaccades and antisaccades tasks. Patients with AD made more antisaccade errors, and corrected fewer errors, than age-matched controls. Error rates, corrected or uncorrected, were not correlated with AD MMSE or Dementia Rating Scale scores. Our findings indicate that antisaccade impairments exist in mild AD, suggesting clinically detectable DLPFC pathology may be present earlier than suggested by previous studies.
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spelling pubmed-33432952012-05-09 Executive deficits detected in mild Alzheimer's disease using the antisaccade task Kaufman, Liam D Pratt, Jay Levine, Brian Black, Sandra E Brain Behav Original Research The antisaccade task, a hands- and language-free metric, may provide a functional index of the dorsolateral prefrontal cortex (DLPFC), a region damaged in the later stages of Alzheimer's disease (AD). Our objective was to determine if patients with mild AD made more errors relative to age-matched controls. Thirty patients with mild AD (Mini Mental Status Exam [MMSE] ≥ 17) and 31 age-matched controls completed a laptop version of the prosaccades and antisaccades tasks. Patients with AD made more antisaccade errors, and corrected fewer errors, than age-matched controls. Error rates, corrected or uncorrected, were not correlated with AD MMSE or Dementia Rating Scale scores. Our findings indicate that antisaccade impairments exist in mild AD, suggesting clinically detectable DLPFC pathology may be present earlier than suggested by previous studies. Blackwell Publishing Inc 2012-01 /pmc/articles/PMC3343295/ /pubmed/22574270 http://dx.doi.org/10.1002/brb3.28 Text en © 2011 The Authors. Published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Research
Kaufman, Liam D
Pratt, Jay
Levine, Brian
Black, Sandra E
Executive deficits detected in mild Alzheimer's disease using the antisaccade task
title Executive deficits detected in mild Alzheimer's disease using the antisaccade task
title_full Executive deficits detected in mild Alzheimer's disease using the antisaccade task
title_fullStr Executive deficits detected in mild Alzheimer's disease using the antisaccade task
title_full_unstemmed Executive deficits detected in mild Alzheimer's disease using the antisaccade task
title_short Executive deficits detected in mild Alzheimer's disease using the antisaccade task
title_sort executive deficits detected in mild alzheimer's disease using the antisaccade task
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343295/
https://www.ncbi.nlm.nih.gov/pubmed/22574270
http://dx.doi.org/10.1002/brb3.28
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