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Spatial navigation deficits in early Alzheimer's disease: the role of biomarkers and APOE genotype

Spatial navigation deficits in early Alzheimer's disease: the role of biomarkers and APOE genotype
Spatial navigation deficits in early Alzheimer's disease: the role of biomarkers and APOE genotype

BACKGROUND: Spatial navigation deficits are early symptoms of Alzheimer's disease (AD). The apolipoprotein E (APOE) ε4 allele is the most important genetic risk factor for AD. This study investigated effects of APOE genotype on spatial navigation in biomarker-defined individuals with amnestic mild cognitive impairment (aMCI) and associations of AD biomarkers and atrophy of AD-related brain regions with spatial navigation.

METHODS: 107 participants, cognitively normal older adults (CN, n = 48) and aMCI individuals stratified into AD aMCI (n = 28) and non-AD aMCI (n = 31) groups, underwent cognitive assessment, brain MRI, and spatial navigation assessment using the Virtual Supermarket Test with egocentric and allocentric tasks and a self-report questionnaire. Cerebrospinal fluid (CSF) biomarkers (amyloid-β1-42, phosphorylated tau181 and total tau) and amyloid PET imaging were assessed in aMCI participants.

RESULTS: AD aMCI participants had the highest prevalence of APOE ε4 carriers and worst allocentric navigation. CSF levels of AD biomarkers and atrophy in AD-related brain regions were associated with worse allocentric navigation. Between-group differences in spatial navigation and associations with AD biomarkers and regional brain atrophy were not influenced by APOE genotype. Self-reported navigation ability was similar across groups and unrelated to spatial navigation performance.

CONCLUSIONS: These findings suggest that allocentric navigation deficits in aMCI individuals are predominantly driven by AD pathology, independent of APOE genotype. This highlights the role of AD pathology as measured by biomarkers, rather than genetic status, as a major factor in navigational impairment in aMCI, and emphasizes the assessment of spatial navigation as a valuable tool for early detection of AD.

Aged, Aged, 80 and over, Alzheimer Disease/genetics, Amyloid beta-Peptides/cerebrospinal fluid, Apolipoprotein E4/genetics, Apolipoproteins E/genetics, Atrophy, Biomarkers/cerebrospinal fluid, Brain/pathology, Cognitive Dysfunction/genetics, Female, Genotype, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Peptide Fragments/cerebrospinal fluid, Positron-Emission Tomography, Spatial Navigation/physiology, tau Proteins/cerebrospinal fluid
0340-5354
Laczó, Martina
3ebc60dc-18a9-4ade-ae64-587a70d34773
Svacova, Zuzana
e450dad5-6424-4e98-9fbb-33428d7db163
Lerch, Ondrej
dafcefa1-0241-4978-947b-5fa001c2c114
Martinkovic, Lukas
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Krejci, Monika
aa790f89-f68c-476b-bd69-78409d0a70d4
Nedelska, Zuzana
03b5da9a-9b79-4925-b044-2c35c00a7108
Horakova, Hana
c9283946-2027-4a0a-8a44-468326269db5
Matoska, Vaclav
e0059352-a82c-4c60-bf5c-38c4a53afa23
Vyhnalek, Martin
871fd842-1121-42e5-9602-93532dbd77b1
Hort, Jakub
c90bd65d-a849-4f2b-82e0-aba473036666
Hornberger, Michael
a48c1c63-422a-4c11-9a51-c7be0aa3026d
Laczó, Jan
ee53276e-e401-4a17-b0ab-58efab82defc
Laczó, Martina
3ebc60dc-18a9-4ade-ae64-587a70d34773
Svacova, Zuzana
e450dad5-6424-4e98-9fbb-33428d7db163
Lerch, Ondrej
dafcefa1-0241-4978-947b-5fa001c2c114
Martinkovic, Lukas
dd3be6c4-74ed-4219-abbf-977a4e20eb42
Krejci, Monika
aa790f89-f68c-476b-bd69-78409d0a70d4
Nedelska, Zuzana
03b5da9a-9b79-4925-b044-2c35c00a7108
Horakova, Hana
c9283946-2027-4a0a-8a44-468326269db5
Matoska, Vaclav
e0059352-a82c-4c60-bf5c-38c4a53afa23
Vyhnalek, Martin
871fd842-1121-42e5-9602-93532dbd77b1
Hort, Jakub
c90bd65d-a849-4f2b-82e0-aba473036666
Hornberger, Michael
a48c1c63-422a-4c11-9a51-c7be0aa3026d
Laczó, Jan
ee53276e-e401-4a17-b0ab-58efab82defc

Laczó, Martina, Svacova, Zuzana, Lerch, Ondrej, Martinkovic, Lukas, Krejci, Monika, Nedelska, Zuzana, Horakova, Hana, Matoska, Vaclav, Vyhnalek, Martin, Hort, Jakub, Hornberger, Michael and Laczó, Jan (2025) Spatial navigation deficits in early Alzheimer's disease: the role of biomarkers and APOE genotype. Journal of Neurology, 272 (6), [438]. (doi:10.1007/s00415-025-13151-8).

Record type: Article

Abstract

BACKGROUND: Spatial navigation deficits are early symptoms of Alzheimer's disease (AD). The apolipoprotein E (APOE) ε4 allele is the most important genetic risk factor for AD. This study investigated effects of APOE genotype on spatial navigation in biomarker-defined individuals with amnestic mild cognitive impairment (aMCI) and associations of AD biomarkers and atrophy of AD-related brain regions with spatial navigation.

METHODS: 107 participants, cognitively normal older adults (CN, n = 48) and aMCI individuals stratified into AD aMCI (n = 28) and non-AD aMCI (n = 31) groups, underwent cognitive assessment, brain MRI, and spatial navigation assessment using the Virtual Supermarket Test with egocentric and allocentric tasks and a self-report questionnaire. Cerebrospinal fluid (CSF) biomarkers (amyloid-β1-42, phosphorylated tau181 and total tau) and amyloid PET imaging were assessed in aMCI participants.

RESULTS: AD aMCI participants had the highest prevalence of APOE ε4 carriers and worst allocentric navigation. CSF levels of AD biomarkers and atrophy in AD-related brain regions were associated with worse allocentric navigation. Between-group differences in spatial navigation and associations with AD biomarkers and regional brain atrophy were not influenced by APOE genotype. Self-reported navigation ability was similar across groups and unrelated to spatial navigation performance.

CONCLUSIONS: These findings suggest that allocentric navigation deficits in aMCI individuals are predominantly driven by AD pathology, independent of APOE genotype. This highlights the role of AD pathology as measured by biomarkers, rather than genetic status, as a major factor in navigational impairment in aMCI, and emphasizes the assessment of spatial navigation as a valuable tool for early detection of AD.

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Accepted/In Press date: 5 May 2025
Published date: 2 June 2025
Additional Information: © 2025. The Author(s).
Keywords: Aged, Aged, 80 and over, Alzheimer Disease/genetics, Amyloid beta-Peptides/cerebrospinal fluid, Apolipoprotein E4/genetics, Apolipoproteins E/genetics, Atrophy, Biomarkers/cerebrospinal fluid, Brain/pathology, Cognitive Dysfunction/genetics, Female, Genotype, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Peptide Fragments/cerebrospinal fluid, Positron-Emission Tomography, Spatial Navigation/physiology, tau Proteins/cerebrospinal fluid

Identifiers

Local EPrints ID: 505345
URI: http://eprints.soton.ac.uk/id/eprint/505345
ISSN: 0340-5354
PURE UUID: 5be51c0c-076f-481d-ba5c-a39bf7fb5408
ORCID for Michael Hornberger: ORCID iD orcid.org/0000-0002-2214-3788

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Date deposited: 07 Oct 2025 16:38
Last modified: 08 Oct 2025 02:17

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Contributors

Author: Martina Laczó
Author: Zuzana Svacova
Author: Ondrej Lerch
Author: Lukas Martinkovic
Author: Monika Krejci
Author: Zuzana Nedelska
Author: Hana Horakova
Author: Vaclav Matoska
Author: Martin Vyhnalek
Author: Jakub Hort
Author: Michael Hornberger ORCID iD
Author: Jan Laczó

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