Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/26984
Title: Associations between Neuropsychiatric Symptoms and Alzheimer’s Disease Biomarkers in People with Mild Cognitive Impairment
Authors: Arenare, G
Manca, R
Caffarra, P
Venneri, A
Keywords: neuropsychiatric symptoms;mild cognitive impairment;biomarkers;amyloid;tau;neurodegeneration
Issue Date: 12-Aug-2023
Publisher: MDPI
Citation: Arenare, 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.
Abstract: Background: 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.
Description: Data Availability Statement: All ADNI data are made publicly available upon request.
URI: https://bura.brunel.ac.uk/handle/2438/26984
DOI: https://doi.org/10.3390/brainsci13081195
Other Identifiers: ORCiD: Riccardo Manca https://orcid.org/0000-0003-1715-6442
ORCiD: Annalena Venneri https://orcid.org/0000-0002-9488-2301
1195
Appears in Collections:Dept of Life Sciences Research Papers

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