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Toward personalized cognitive diagnostics of at-genetic-risk Alzheimer's disease

Toward personalized cognitive diagnostics of at-genetic-risk Alzheimer's disease
Toward personalized cognitive diagnostics of at-genetic-risk Alzheimer's disease
Spatial navigation is emerging as a critical factor in identifying preclinical Alzheimer’s disease (AD). However, the impact of interindividual navigation ability and demographic risk factors (e.g., APOE, age, and sex) on spatial navigation make it difficult to identify persons “at high risk” of AD in the preclinical stages. In the current study, we use spatial navigation big data (n = 27,108) from the Sea Hero Quest (SHQ) game to overcome these challenges by investigating whether big data can be used to benchmark a highly phenotyped healthy aging laboratory cohort into high- vs. low-risk persons based on their genetic (APOE) and demographic (sex, age, and educational attainment) risk factors. Our results replicate previous findings in APOE ε4 carriers, indicative of grid cell coding errors in the entorhinal cortex, the initial brain region affected by AD pathophysiology. We also show that although baseline navigation ability differs between men and women, sex does not interact with the APOE genotype to influence the manifestation of AD-related spatial disturbance. Most importantly, we demonstrate that such high-risk preclinical cases can be reliably distinguished from low-risk participants using big-data spatial navigation benchmarks. By contrast, participants were undistinguishable on neuropsychological episodic memory tests. Taken together, we present evidence to suggest that, in the future, SHQ normative benchmark data can be used to more accurately classify spatial impairments in at-high-risk of AD healthy participants at a more individual level, therefore providing the steppingstone for individualized diagnostics and outcome measures of cognitive symptoms in preclinical AD.
0027-8424
9285-9292
Coughlan, G
d202a575-3974-4929-9010-b4d946578bba
Coutrot, A
54489887-62d2-47a6-8dd8-23e46d746f2d
Khondoker, M
e849cf3f-c8b2-49ea-b2d4-d1da9bb16596
AM, Minihane
b9541773-aac8-4d70-ab1d-36fe58e42389
Spiers, H
558afa7b-d842-4ca7-a66e-eff8e11f1538
Hornberger, M
a48c1c63-422a-4c11-9a51-c7be0aa3026d
Coughlan, G
d202a575-3974-4929-9010-b4d946578bba
Coutrot, A
54489887-62d2-47a6-8dd8-23e46d746f2d
Khondoker, M
e849cf3f-c8b2-49ea-b2d4-d1da9bb16596
AM, Minihane
b9541773-aac8-4d70-ab1d-36fe58e42389
Spiers, H
558afa7b-d842-4ca7-a66e-eff8e11f1538
Hornberger, M
a48c1c63-422a-4c11-9a51-c7be0aa3026d

Coughlan, G, Coutrot, A, Khondoker, M, AM, Minihane, Spiers, H and Hornberger, M (2019) Toward personalized cognitive diagnostics of at-genetic-risk Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America, 116 (19), 9285-9292. (doi:10.1073/pnas.1901600116).

Record type: Article

Abstract

Spatial navigation is emerging as a critical factor in identifying preclinical Alzheimer’s disease (AD). However, the impact of interindividual navigation ability and demographic risk factors (e.g., APOE, age, and sex) on spatial navigation make it difficult to identify persons “at high risk” of AD in the preclinical stages. In the current study, we use spatial navigation big data (n = 27,108) from the Sea Hero Quest (SHQ) game to overcome these challenges by investigating whether big data can be used to benchmark a highly phenotyped healthy aging laboratory cohort into high- vs. low-risk persons based on their genetic (APOE) and demographic (sex, age, and educational attainment) risk factors. Our results replicate previous findings in APOE ε4 carriers, indicative of grid cell coding errors in the entorhinal cortex, the initial brain region affected by AD pathophysiology. We also show that although baseline navigation ability differs between men and women, sex does not interact with the APOE genotype to influence the manifestation of AD-related spatial disturbance. Most importantly, we demonstrate that such high-risk preclinical cases can be reliably distinguished from low-risk participants using big-data spatial navigation benchmarks. By contrast, participants were undistinguishable on neuropsychological episodic memory tests. Taken together, we present evidence to suggest that, in the future, SHQ normative benchmark data can be used to more accurately classify spatial impairments in at-high-risk of AD healthy participants at a more individual level, therefore providing the steppingstone for individualized diagnostics and outcome measures of cognitive symptoms in preclinical AD.

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Published date: April 2019

Identifiers

Local EPrints ID: 504884
URI: http://eprints.soton.ac.uk/id/eprint/504884
ISSN: 0027-8424
PURE UUID: c4aa87fb-fdd0-4dd1-938f-5fefa7a58c21
ORCID for M Hornberger: ORCID iD orcid.org/0000-0002-2214-3788

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Date deposited: 19 Sep 2025 17:18
Last modified: 20 Sep 2025 02:31

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Contributors

Author: G Coughlan
Author: A Coutrot
Author: M Khondoker
Author: Minihane AM
Author: H Spiers
Author: M Hornberger ORCID iD

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