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dc.contributor.authorCreese, B
dc.contributor.authorArathimos, R
dc.contributor.authorBrooker, H
dc.contributor.authorAarsland, D
dc.contributor.authorCorbett, A
dc.contributor.authorLewis, C
dc.contributor.authorBallard, C
dc.contributor.authorIsmail, Z
dc.date.accessioned2021-01-26T14:56:46Z
dc.date.issued2021-03-17
dc.description.abstractBACKGROUND: The neuropsychiatric syndrome Mild Behavioral Impairment (MBI) describes an at-risk state for dementia and may be a useful screening tool for sample enrichment. We hypothesized that stratifying a cognitively normal sample on MBI status would enhance the association between genetic risk for Alzheimer’s disease (AD) and cognition. METHODS: Data from 4,458 participants over 50 without dementia was analysed. A cognitive composite score was constructed and the MBI Checklist was used to stratify into those with MBI and those without. Polygenic scores for AD were generated using summary statistics from the IGAP study. RESULTS: AD genetic risk was associated with worse cognition in the MBI group but not in the no MBI group (MBI: β=-0.09, 95% CI: -0.13 - -0.03, p=0.002, R =0.003). The strongest association was in those with more severe MBI aged ≥65. CONCLUSIONS: MBI is an important feature of aging, screening on MBI may be a useful sample enrichment strategy for clinical research.en_GB
dc.description.sponsorshipNational Institute for Health Research (NIHR)en_GB
dc.identifier.citationVol. 13 (1), article e12164en_GB
dc.identifier.doi10.1002/dad2.12164
dc.identifier.urihttp://hdl.handle.net/10871/124509
dc.language.isoenen_GB
dc.publisherWiley / Alzheimer's Associationen_GB
dc.rights© 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
dc.subjectmild behavioral impairmenten_GB
dc.subjectpolygenic scoreen_GB
dc.subjectAlzheimer’s diseaseen_GB
dc.subjectneuropsychiatric symptomsen_GB
dc.subjectcognitionen_GB
dc.titleGenetic risk for Alzheimer’s disease, cognition and mild behavioral impairment in healthy older adultsen_GB
dc.typeArticleen_GB
dc.date.available2021-01-26T14:56:46Z
dc.identifier.issn2352-8729
dc.descriptionThis is the final version. Available on open access from Wiley via the DOI in this recorden_GB
dc.identifier.journalAlzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoringen_GB
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dcterms.dateAccepted2021-01-26
exeter.funder::Medical Research Council (MRC)en_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2021-01-26
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2021-01-26T14:16:56Z
refterms.versionFCDAM
refterms.dateFOA2021-03-23T14:11:41Z
refterms.panelAen_GB


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© 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association.

This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
Except where otherwise noted, this item's licence is described as © 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.