Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/26984
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dc.contributor.authorArenare, G-
dc.contributor.authorManca, R-
dc.contributor.authorCaffarra, P-
dc.contributor.authorVenneri, A-
dc.contributor.otherAlzheimer’s Disease Neuroimaging Initiative-
dc.date.accessioned2023-08-17T16:20:44Z-
dc.date.available2023-08-17T16:20:44Z-
dc.date.issued2023-08-12-
dc.identifierORCiD: Riccardo Manca https://orcid.org/0000-0003-1715-6442-
dc.identifierORCiD: Annalena Venneri https://orcid.org/0000-0002-9488-2301-
dc.identifier1195-
dc.identifier.citationArenare, G. et al. on behalf of the Alzheimer’s Disease Neuroimaging Initiative (2023) 'Associations between Neuropsychiatric Symptoms and Alzheimer’s Disease Biomarkers in People with Mild Cognitive Impairment', Brain Sciences, 13 (8), 1195, pp. 1 - 11. doi: 10.3390/brainsci13081195.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/26984-
dc.descriptionData Availability Statement: All ADNI data are made publicly available upon request.en_US
dc.description.abstractBackground: Neuropsychiatric symptoms (NPS) are associated with faster decline in mild cognitive impairment (MCI). This study aimed to investigate the association between NPS severity and Alzheimer’s disease (AD) biomarkers, i.e., amyloid-β (Aβ), phosphorylated tau protein (p-tau) and hippocampal volume ratio (HR), to characterise in more detail MCI patients with a poor prognosis. Methods: A total of 506 individuals with MCI and 99 cognitively unimpaired older adults were selected from the ADNI dataset. The patients were divided into three different groups based on their NPI-Q total scores: no NPS (n = 198), mild NPS (n = 160) and severe NPS (n = 148). Regression models were used to assess the association between the severity of NPS and each biomarker level and positivity status. Results: Cerebrospinal fluid Aβ levels were positively associated with older age and lower MMSE scores, while higher p-tau levels were associated with female sex and lower MMSE scores. Only patients with severe NPS had a lower HR (β = −0.18, p = 0.050), i.e., more pronounced medio-temporal atrophy, than those without NPS. Discussion: Only HR was associated with the presence of NPS, partially in line with previous evidence showing that severe NPS may be explained primarily by greater grey matter loss. Future longitudinal studies will be needed to ascertain the relevance of this finding.en_US
dc.description.sponsorshipThe data collection and sharing for this project were funded by the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense, award number W81XWH-12-2-0012). The ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd. and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosi-ty; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support the ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org (accessed on 10 July 2023)). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California. R.M. acknowledges the support received through a research fellowship from the Alzheimer’s Association.en_US
dc.format.extent1 - 11-
dc.format.mediumElectronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherMDPIen_US
dc.rightsCopyright © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectneuropsychiatric symptomsen_US
dc.subjectmild cognitive impairmenten_US
dc.subjectbiomarkersen_US
dc.subjectamyloiden_US
dc.subjecttauen_US
dc.subjectneurodegenerationen_US
dc.titleAssociations between Neuropsychiatric Symptoms and Alzheimer’s Disease Biomarkers in People with Mild Cognitive Impairmenten_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.3390/brainsci13081195-
dc.relation.isPartOfBrain Sciences-
pubs.issue8-
pubs.publication-statusPublished online-
pubs.volume13-
dc.identifier.eissn2076-3425-
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/legalcode.en-
dc.rights.holderThe authors-
Appears in Collections:Dept of Life Sciences Research Papers

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