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Associations between multidomain modifiable dementia risk factors with AD biomarkers and cognition in middle-aged and older adults.
- Source :
-
Neurobiology of Aging . Jun2024, Vol. 138, p63-71. 9p. - Publication Year :
- 2024
-
Abstract
- This study aimed to determine associations between modifiable dementia risk factors (MDRF), across domains mood symptomatology, lifestyle behaviors, cardiovascular conditions, cognitive/social engagement, sleep disorders/symptomatology, with cognition, beta-amyloid (Aβ) and tau, and brain volume. Middle-aged/older adults (n=82) enrolled in a sub-study of the Healthy Brain Project completed self-report questionnaires and a neuropsychological battery. Cerebrospinal fluid levels of Aβ 1–42, total tau (t-tau), and phosphorylated tau (p-tau 181) (Roche Elecsys), and MRI markers of hippocampal volume and total brain volume were obtained. Participants were classified as no/single domain risk (≤1 domains) or multidomain risk (≥2 domains). Compared to the no/single domain risk group, the multidomain risk group performed worse on the Preclinical Alzheimer's Cognitive Composite (d=0.63, p=.005), and Executive Function (d=0.50, p=.016), and had increased p-tau 181 (d=0.47, p=.042) and t-tau (d=0.54, p=.021). In middle-aged/older adults, multidomain MDRFs were related to increases in tau and worse cognition, but not Aβ or brain volume. Findings suggest that increases in AD biomarkers are apparent in midlife, particularly for individuals with greater burden, or variety of MDRFs. • Modifiable dementia risk factors (MDRF) were classified into five risk domains. • Multidomain MDRFs were associated with increased tau and worse cognition. • MDRF-related increases in Alzheimer's disease (AD) biomarkers occur in midlife. • Multidomain MDRF and cognition association is not fully explained by AD biomarkers. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 01974580
- Volume :
- 138
- Database :
- Academic Search Index
- Journal :
- Neurobiology of Aging
- Publication Type :
- Academic Journal
- Accession number :
- 176471156
- Full Text :
- https://doi.org/10.1016/j.neurobiolaging.2024.02.015