Document Type

Journal Article

Publisher

Hindawi

School

School of Medical and Health Sciences

RAS ID

25279

Funders

National Health and Medical Research Council (NHMRC)

CSIRO Flagship Collaboration Fund

Science and Industry Endowment Fund (SIEF) in partnership with Edith Cowan University (ECU)

Florey Institute of Neuroscience and Mental Health, Alzheimer’s Australia (AA)

National Ageing Research Institute (NARI)

Austin Health

CogState Ltd.

Hollywood Private Hospital

Sir Charles Gairdner Hospital

Dementia Collaborative Research Centres program (DCRC2)

Cooperative Research Centre (CRC) for Mental Health—funded through the CRC program (an Australian Government Initiative, Grant ID 20100104)

McCusker Alzheimer’s Research Foundation

Operational Infrastructure Support from the Government of Victoria

Comments

Frost, S., Robinson, L., Rowe, C. C., Ames, D., Masters, C. L., Taddei, K., ... & Kanagasingam, Y. (2017). Evaluation of cholinergic deficiency in preclinical Alzheimer’s disease using pupillometry. Journal of Ophthalmology, 2017.

https://doi.org/10.1155/2017/7935406

Abstract

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.

DOI

10.1155/2017/7935406

Creative Commons License

Creative Commons Attribution 4.0 License
This work is licensed under a Creative Commons Attribution 4.0 License.

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