Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18444
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dc.contributor.authorFrost, Shaun-
dc.contributor.authorRobinson, Liam-
dc.contributor.authorRowe, Christopher C-
dc.contributor.authorAmes, David-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorTaddei, Kevin-
dc.contributor.authorRainey-Smith, Stephanie R-
dc.contributor.authorMartins, Ralph N-
dc.contributor.authorKanagasingam, Yogesan-
dc.date2017-08-16-
dc.date.accessioned2018-08-30T06:04:41Z-
dc.date.available2018-08-30T06:04:41Z-
dc.date.issued2017-
dc.identifier.citationJournal of ophthalmology 2017; 2017: 7935406-
dc.identifier.issn2090-004X-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18444-
dc.description.abstractCortical 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.-
dc.language.isoeng-
dc.titleEvaluation of Cholinergic Deficiency in Preclinical Alzheimer's Disease Using Pupillometry.-
dc.typeJournal Article-
dc.identifier.journaltitleJournal of ophthalmology-
dc.identifier.affiliationSchool of Psychiatry and Clinical Neurosciences, University of Western Australia, Australia, Crawley, WA, Australiaen
dc.identifier.affiliationDepartment of Psychiatry, University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationThe Mental Health Research Institute (MHRI), University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationSchool of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australiaen
dc.identifier.affiliationSir James McCusker Alzheimer's Disease Research Unit, Hollywood Private Hospital, Perth, WA, Australiaen
dc.identifier.affiliationSchool of Biomedical Sciences, Macquarie University, North Ryde, NSW, Australiaen
dc.identifier.affiliationNational Ageing Research Institute, Melbourne, Victoria, Australiaen
dc.identifier.affiliationAustralian e-Health Research Centre, Perth, WA, Australiaen
dc.identifier.affiliationDepartment of Nuclear Medicine and Centre for PET, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationCommonwealth Scientific and Industrial Research Organisation (CSIRO), Perth, WA, Australiaen
dc.identifier.doi10.1155/2017/7935406-
dc.identifier.orcid0000-0002-1681-8224-
dc.identifier.orcid0000-0003-3910-2453-
dc.identifier.pubmedid28894607-
dc.type.austinJournal Article-
local.name.researcherMasters, Colin L
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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