Abstract:
:We investigated whether (1) serum levels of 25-hydroxyvitamin D [25(OH)D] and single nucleotide polymorphisms (SNPs) in the group-specific component (GC) gene-regulating serum 25(OH)D levels are associated with cognition in older individuals; and (2) whether causal relationships exist between 25(OH)D and cognition during aging. Data from 1207 participants in the Baltimore Longitudinal Study of Aging were analyzed (mean follow-up, 10.4 years) to test associations between serum 25(OH)D and cognition. Two GC SNPs were used to derive a composite genetic risk score associated with lower 25(OH)D concentrations. Lower serum 25(OH)D and higher GC composite scores were associated with lower executive function at baseline. Mendelian randomization analyses suggested a causal relationship between lower serum 25(OH)D and poorer executive function and psychomotor speed. The SNP score was also associated with lower performance on measures of visuospatial abilities at baseline but with attenuated declines over time in visuospatial abilities and executive function. Widespread associations between vitamin-D regulatory SNPs and cognition suggest a mechanistic basis for the relationship between serum 25(OH)D levels and cognition during aging.
journal_name
Neurobiol Agingjournal_title
Neurobiology of agingauthors
Kueider AM,Tanaka T,An Y,Kitner-Triolo MH,Palchamy E,Ferrucci L,Thambisetty Mdoi
10.1016/j.neurobiolaging.2015.11.002subject
Has Abstractpub_date
2016-03-01 00:00:00pages
38-45eissn
0197-4580issn
1558-1497pii
S0197-4580(15)00554-0journal_volume
39pub_type
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