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Interactive Associations of Neuropsychiatry Inventory-Questionnaire Assessed Sleep Disturbance and Vascular Risk on Alzheimer's Disease Stage Progression in Clinically Normal Older Adults.

Authors :
Bubu OM
Williams ET
Umasabor-Bubu OQ
Kaur SS
Turner AD
Blanc J
Cejudo JR
Mullins AE
Parekh A
Kam K
Osakwe ZT
Nguyen AW
Trammell AR
Mbah AK
de Leon M
Rapoport DM
Ayappa I
Ogedegbe G
Jean-Louis G
Masurkar AV
Varga AW
Osorio RS
Source :
Frontiers in aging neuroscience [Front Aging Neurosci] 2021 Dec 10; Vol. 13, pp. 763264. Date of Electronic Publication: 2021 Dec 10 (Print Publication: 2021).
Publication Year :
2021

Abstract

Background: To determine whether sleep disturbance (SD) and vascular-risk interact to promote Alzheimer's disease (AD) stage-progression in normal, community-dwelling older adults and evaluate their combined risk beyond that of established AD biomarkers. Methods: Longitudinal data from the National Alzheimer's Coordinating Center Uniform-Dataset. SD data (i.e., SD+ vs. SD-), as characterized by the Neuropsychiatric Inventory-Questionnaire, were derived from 10,600 participants at baseline, with at-least one follow-up visit. A subset ( n = 361) had baseline cerebrospinal fluid (CSF) biomarkers and MRI data. The Framingham heart study general cardiovascular disease (FHS-CVD) risk-score was used to quantify vascular risk. Amnestic mild cognitive impairment (aMCI) diagnosis during follow-up characterized AD stage-progression. Logistic mixed-effects models with random intercept and slope examined the interaction of SD and vascular risk on prospective aMCI diagnosis. Results: Of the 10,600 participants, 1,017 (9.6%) reported SD and 6,572 (62%) were female. The overall mean (SD) age was 70.5 (6.5), and follow-up time was 5.1 (2.7) years. SD and the FHS-CVD risk-score were each associated with incident aMCI (aOR: 1.42 and aOR: 2.11, p < 0.01 for both). The interaction of SD and FHS-CVD risk-score with time was significant (aOR: 2.87, p < 0.01), suggesting a synergistic effect. SD and FHS-CVD risk-score estimates remained significantly associated with incident aMCI even after adjusting for CSF (Aβ, T-tau, P-tau) and hippocampal volume ( n = 361) (aOR: 2.55, p < 0.01), and approximated risk-estimates of each biomarker in the sample where data was available. Conclusions: Clinical measures of sleep and vascular risk may complement current AD biomarkers in assessing risk of cognitive decline in older adults.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Bubu, Williams, Umasabor-Bubu, Kaur, Turner, Blanc, Cejudo, Mullins, Parekh, Kam, Osakwe, Nguyen, Trammell, Mbah, de Leon, Rapoport, Ayappa, Ogedegbe, Jean-Louis, Masurkar, Varga and Osorio.)

Details

Language :
English
ISSN :
1663-4365
Volume :
13
Database :
MEDLINE
Journal :
Frontiers in aging neuroscience
Publication Type :
Academic Journal
Accession number :
34955813
Full Text :
https://doi.org/10.3389/fnagi.2021.763264