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Evaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry

Cortical cholinergic deficiency is prominent in Alzheimer's disease (AD), and published findings of diminished pupil flash response in AD suggest that this deficiency may extend to the visual cortical areas and anterior eye. Pupillometry is a low-cost, noninvasive technique that may be useful f...

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Autores principales: Frost, Shaun, Robinson, Liam, Rowe, Christopher C., Ames, David, Masters, Colin L., Taddei, Kevin, Rainey-Smith, Stephanie R., Martins, Ralph N., Kanagasingam, Yogesan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574262/
https://www.ncbi.nlm.nih.gov/pubmed/28894607
http://dx.doi.org/10.1155/2017/7935406
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author Frost, Shaun
Robinson, Liam
Rowe, Christopher C.
Ames, David
Masters, Colin L.
Taddei, Kevin
Rainey-Smith, Stephanie R.
Martins, Ralph N.
Kanagasingam, Yogesan
author_facet Frost, Shaun
Robinson, Liam
Rowe, Christopher C.
Ames, David
Masters, Colin L.
Taddei, Kevin
Rainey-Smith, Stephanie R.
Martins, Ralph N.
Kanagasingam, Yogesan
author_sort Frost, Shaun
collection PubMed
description Cortical cholinergic deficiency is prominent in Alzheimer's disease (AD), and published findings of diminished pupil flash response in AD suggest that this deficiency may extend to the visual cortical areas and anterior eye. Pupillometry is a low-cost, noninvasive technique that may be useful for monitoring cholinergic deficits which generally lead to memory and cognitive disorders. The aim of the study was to evaluate pupillometry for early detection of AD by comparing the pupil flash response (PFR) in AD (N = 14) and cognitively normal healthy control (HC, N = 115) participants, with the HC group stratified according to high (N = 38) and low (N = 77) neocortical amyloid burden (NAB). Constriction phase PFR parameters were significantly reduced in AD compared to HC (maximum acceleration p < 0.05, maximum velocity p < 0.0005, average velocity p < 0.005, and constriction amplitude p < 0.00005). The high-NAB HC subgroup had reduced PFR response cross-sectionally, and also a greater decline longitudinally, compared to the low-NAB subgroup, suggesting changes to pupil response in preclinical AD. The results suggest that PFR changes may occur in the preclinical phase of AD. Hence, pupillometry has a potential as an adjunct for noninvasive, cost-effective screening for preclinical AD.
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spelling pubmed-55742622017-09-11 Evaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry Frost, Shaun Robinson, Liam Rowe, Christopher C. Ames, David Masters, Colin L. Taddei, Kevin Rainey-Smith, Stephanie R. Martins, Ralph N. Kanagasingam, Yogesan J Ophthalmol Research Article Cortical cholinergic deficiency is prominent in Alzheimer's disease (AD), and published findings of diminished pupil flash response in AD suggest that this deficiency may extend to the visual cortical areas and anterior eye. Pupillometry is a low-cost, noninvasive technique that may be useful for monitoring cholinergic deficits which generally lead to memory and cognitive disorders. The aim of the study was to evaluate pupillometry for early detection of AD by comparing the pupil flash response (PFR) in AD (N = 14) and cognitively normal healthy control (HC, N = 115) participants, with the HC group stratified according to high (N = 38) and low (N = 77) neocortical amyloid burden (NAB). Constriction phase PFR parameters were significantly reduced in AD compared to HC (maximum acceleration p < 0.05, maximum velocity p < 0.0005, average velocity p < 0.005, and constriction amplitude p < 0.00005). The high-NAB HC subgroup had reduced PFR response cross-sectionally, and also a greater decline longitudinally, compared to the low-NAB subgroup, suggesting changes to pupil response in preclinical AD. The results suggest that PFR changes may occur in the preclinical phase of AD. Hence, pupillometry has a potential as an adjunct for noninvasive, cost-effective screening for preclinical AD. Hindawi 2017 2017-08-16 /pmc/articles/PMC5574262/ /pubmed/28894607 http://dx.doi.org/10.1155/2017/7935406 Text en Copyright © 2017 Shaun Frost et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Frost, Shaun
Robinson, Liam
Rowe, Christopher C.
Ames, David
Masters, Colin L.
Taddei, Kevin
Rainey-Smith, Stephanie R.
Martins, Ralph N.
Kanagasingam, Yogesan
Evaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry
title Evaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry
title_full Evaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry
title_fullStr Evaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry
title_full_unstemmed Evaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry
title_short Evaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry
title_sort evaluation of cholinergic deficiency in preclinical alzheimer's disease using pupillometry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574262/
https://www.ncbi.nlm.nih.gov/pubmed/28894607
http://dx.doi.org/10.1155/2017/7935406
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