Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/27806
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dc.contributor.authorDe Marco, M-
dc.contributor.authorWright, LM-
dc.contributor.authorValera Bermejo, JM-
dc.contributor.authorFerguson, CE-
dc.date.accessioned2023-12-05T11:22:55Z-
dc.date.available2023-12-05T11:22:55Z-
dc.date.issued2023-11-29-
dc.identifierORCID iD: Matteo De Marco https://orcid.org/0000-0002-9240-8067-
dc.identifier108741-
dc.identifier.citationDe Marco, M. et al. (2023) 'APOE ε4 positivity predicts centrality of episodic memory nodes in patients with mild cognitive impairment: A cohort-based, graph theory-informed study of cognitive networks', Neuropsychologia, 192, 108741, pp. 1 - 11. doi: 10.1016/j.neuropsychologia.2023.108741.en_US
dc.identifier.issn0028-3932-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/27806-
dc.descriptionData availability: Data used in this study was obtained from the National Alzheimer’s Coordinating Center initiative (https://naccdata.org/).en_US
dc.descriptionSupplementary data are available online at: https://www.sciencedirect.com/science/article/pii/S0028393223002750?via=ihub#appsec1 .-
dc.description.abstractCopyright © 2023 The Authors. As network neuroscience can capture the systemic impact of APOE variability at a neuroimaging level, this study investigated the network-based cognitive endophenotypes of ε4-carriers and non-carriers across the continuum between normal ageing and Alzheimer's dementia (AD). We hypothesised that the impact of APOE-ε4 on cognitive functioning can be reliably captured by the measurement of graph-theory centrality. Cognitive networks were calculated in 8118 controls, 3482 MCI patients and 4573 AD patients, recruited in the National Alzheimer's Coordinating Center (NACC) database. Nodal centrality was selected as the neurofunctional readout of interest. ε4-carrier-vs.-non-carrier differences were tested in two independent NACC sub-cohorts assessed with either Version 1 or Version 2 of the Uniform Data Set. A significant APOE-dependant effect emerged from the analysis of the Logical-Memory nodes in MCI patients in both sub-cohorts. While non-carriers showed equal centrality in immediate and delayed recall, the latter was significantly less central among carriers (v1: bootstrapped confidence interval 0.107–0.667, p < 0.001; v2: bootstrapped confidence interval 0.018–0.432, p < 0.001). This indicates that, in carriers, delayed recall was, overall, significantly more weakly correlated with the other cognitive scores. These findings were replicated in the sub-groups of sole amnestic-MCI patients (n = 2971), were independent of differences in network communities, clinical severity or other demographic factors. No effects were found in the other two diagnostic groups. APOE-ε4 influences nodal properties of cognitive networks when patients are clinically classified as MCI. This highlights the importance of characterising the impact of risk factors on the wider cognitive network via network-neuroscience methodologies.en_US
dc.description.sponsorshipNeurocare (United Kingdom), under Grant agreement No. 181924 to MDM; Alzheimer's Association Research Grant (23AARG-1030190) to MDM.en_US
dc.format.extent1 - 11-
dc.format.mediumPrint-Electronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.rightsCopyright © 2023 The Authors. Published by Elsevier Ltd. This is an open access article under a Creative Commons license (https://creativecommons.org/licenses/by/4.0/).-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectcognitionen_US
dc.subjectnetwork neuropsychologyen_US
dc.subjectneuropsychological testsen_US
dc.subjectgeneticsen_US
dc.subjectapolipoproteinen_US
dc.titleAPOE ε4 positivity predicts centrality of episodic memory nodes in patients with mild cognitive impairment: A cohort-based, graph theory-informed study of cognitive networksen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1016/j.neuropsychologia.2023.108741-
dc.relation.isPartOfNeuropsychologia-
pubs.issuein press, pre-proof-
pubs.publication-statusPublished-
pubs.volume192-
dc.identifier.eissn1873-3514-
dc.rights.holderThe Authors-
Appears in Collections:Dept of Life Sciences Research Papers

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