Publication
Association of Serum Vitamin D with the Risk of Incident Dementia and Subclinical Indices of Brain Aging: The Framingham Heart Study
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- Persistent URL
- Last modified
- 02/25/2025
- Type of Material
- Authors
- Language
- English
- Date
- 2016-01-01
- Publisher
- IOS Press
- Publication Version
- Copyright Statement
- © 2016 IOS Press and the authors.
- Final Published Version (URL)
- Title of Journal or Parent Work
- ISSN
- 1387-2877
- Volume
- 51
- Issue
- 2
- Start Page
- 451
- End Page
- 461
- Grant/Funding Information
- Dr Pase is funded by an Australian National Health and Medical Research Council (NHMRC) Early Career Fellowship (APP1089698).
- This work was supported by the Framingham Heart Study’s National Heart, Lung, and Blood Institute contract (N01-HC-25195) and by grants from the National Institute of Neurological Disorders and Stroke (R01 NS17950) and from the National Institute on Aging (R01 AG016495, AG008122, AG033193, AG031287).
- Supplemental Material (URL)
- Abstract
- Background: Identifying nutrition- and lifestyle-based risk factors for cognitive impairment and dementia may aid future primary prevention efforts. Objective: We aimed to examine the association of serum vitamin D levels with incident all-cause dementia, clinically characterized Alzheimer's disease (AD), MRI markers of brain aging, and neuropsychological function. Methods: Framingham Heart Study participants had baseline serum 25-hydroxyvitamin D (25(OH)D) concentrations measured between 1986 and 2001. Vitamin D status was considered both as a continuous variable and dichotomized as deficient (<10ng/mL), or at the cohort-specific 20th and 80th percentiles. Vitamin D was related to the 9-year risk of incident dementia (n=1663), multiple neuropsychological tests (n=1291) and MRI markers of brain volume, white matter hyperintensities and silent cerebral infarcts (n=1139). Results: In adjusted models, participants with vitamin D deficiency (n=104, 8% of the cognitive sample) displayed poorer performance on Trail Making B-A (β=-0.03 to -0.05±0.02) and the Hooper Visual Organization Test (β=-0.09 to -0.12±0.05), indicating poorer executive function, processing speed, and visuo-perceptual skills. These associations remained when vitamin D was examined as a continuous variable or dichotomized at the cohort specific 20th percentile. Vitamin D deficiency was also associated with lower hippocampal volumes (β=-0.01±0.01) but not total brain volume, white matter hyperintensities, or silent brain infarcts. No association was found between vitamin D deficiency and incident all-cause dementia or clinically characterized AD. Conclusions: In this large community-based sample, low 25(OH)D concentrations were associated with smaller hippocampal volume and poorer neuropsychological function.
- Author Notes
- Keywords
- D-RECEPTOR
- HORMONE
- nutritional status
- AMYLOID-BETA
- vitamin D
- Neurosciences & Neurology
- risk factors
- METAANALYSIS
- VASCULAR DEMENTIA
- Life Sciences & Biomedicine
- lifestyle
- dementia
- Alzheimer's disease
- magnetic resonance imaging
- Neurosciences
- brain
- diet
- Science & Technology
- neuropsychology
- NEUROPSYCHOLOGICAL FUNCTION
- COGNITIVE PERFORMANCE
- Research Categories
- Gerontology
- Biology, Neuroscience
- Health Sciences, General
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