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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Last modified
  • 02/25/2025
Type of Material
Authors
    Ioannis Karakis, Emory UniversityMatthew P. Pase, Boston UniversityAlexa Beiser, Boston UniversitySarah L. Booth, Tufts UniversityPaul F. Jacques, Tufts UniversityGail Rogers, Tufts UniversityCharles DeCarli, University of California, DavisRamachandran S. Vasan, Framingham Heart StudyThomas J. Wang, Vanderbilt UniversityJayandra J. Himali, Boston UniversityCedric Annweiler, University of AngersSudha Seshadri, Boston University
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
  • Correspondence to: Dr. Sudha Seshadri and Dr. Matthew P. Pase, Department of Neurology, Boston University School of Medicine, B602, 72 East Concord Street, Boston, MA 02118, USA. Tel.: + 1 617 414 1337; Fax: + 1 617 638 8086; suseshad@bu.edu (Dr. S. Seshadri); Tel.:+ 1 617 638 8064; Fax: + 1 617 638 8086; matthewpase@gmail.com (Dr. M.P. Pase).
Keywords
Research Categories
  • Gerontology
  • Biology, Neuroscience
  • Health Sciences, General

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