The impact of Alzheimer's disease risk factors on the pupillary light response.

Alzheimer’s disease biomarkers dementia early detection neurodegeneration pupil pupillary light response risk factor

Journal

Frontiers in neuroscience
ISSN: 1662-4548
Titre abrégé: Front Neurosci
Pays: Switzerland
ID NLM: 101478481

Informations de publication

Date de publication:
2023
Historique:
received: 27 06 2023
accepted: 31 07 2023
medline: 31 8 2023
pubmed: 31 8 2023
entrez: 31 8 2023
Statut: epublish

Résumé

Alzheimer's disease (AD) is the leading cause of dementia, and its prevalence is increasing and is expected to continue to increase over the next few decades. Because of this, there is an urgent requirement to determine a way to diagnose the disease, and to target interventions to delay and ideally stop the onset of symptoms, specifically those impacting cognition and daily livelihood. The pupillary light response (PLR) is controlled by the sympathetic and parasympathetic branches of the autonomic nervous system, and impairments to the pupillary light response (PLR) have been related to AD. However, most of these studies that assess the PLR occur in patients who have already been diagnosed with AD, rather than those who are at a higher risk for the disease but without a diagnosis. Determining whether the PLR is similarly impaired in subjects before an AD diagnosis is made and before cognitive symptoms of the disease begin, is an important step before using the PLR as a diagnostic tool. Specifically, identifying whether the PLR is impaired in specific at-risk groups, considering both genetic and non-genetic risk factors, is imperative. It is possible that the PLR may be impaired in association with some risk factors but not others, potentially indicating different pathways to neurodegeneration that could be distinguished using PLR. In this work, we review the most common genetic and lifestyle-based risk factors for AD and identify established relationships between these risk factors and the PLR. The evidence here shows that many AD risk factors, including traumatic brain injury, ocular and intracranial hypertension, alcohol consumption, depression, and diabetes, are directly related to changes in the PLR. Other risk factors currently lack sufficient literature to make any conclusions relating directly to the PLR but have shown links to impairments in the parasympathetic nervous system; further research should be conducted in these risk factors and their relation to the PLR.

Identifiants

pubmed: 37650103
doi: 10.3389/fnins.2023.1248640
pmc: PMC10463762
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1248640

Informations de copyright

Copyright © 2023 Sparks, Pinto, Hayes, Spitschan and Bulte.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Sierra Sparks (S)

Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.

Joana Pinto (J)

Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.

Genevieve Hayes (G)

Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.

Manuel Spitschan (M)

TUM Department of Sport and Health Sciences (TUM SG), Chronobiology and Health, Technical University of Munich, Munich, Germany.
TUM Institute for Advanced Study (TUM-IAS), Technical University of Munich, Garching, Germany.
Max Planck Institute for Biological Cybernetics, Translational Sensory and Circadian Neuroscience, Tübingen, Germany.

Daniel P Bulte (DP)

Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.

Classifications MeSH