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Vitamin D Synthesis Following a Single Bout of Sun Exposure in Older and Younger Men and Women

Older adults are frequently cited as an at-risk population for vitamin D deficiency that may in part be due to decreased cutaneous synthesis, a potentially important source of cholecalciferol (vitamin D(3)). Previous studies found that cutaneous D(3) production declines with age; however, most studi...

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Detalles Bibliográficos
Autores principales: Chalcraft, Jenna R., Cardinal, Linda M., Wechsler, Perry J., Hollis, Bruce W., Gerow, Kenneth G., Alexander, Brenda M., Keith, Jill F., Larson-Meyer, D. Enette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468901/
https://www.ncbi.nlm.nih.gov/pubmed/32727044
http://dx.doi.org/10.3390/nu12082237
Descripción
Sumario:Older adults are frequently cited as an at-risk population for vitamin D deficiency that may in part be due to decreased cutaneous synthesis, a potentially important source of cholecalciferol (vitamin D(3)). Previous studies found that cutaneous D(3) production declines with age; however, most studies have been conducted ex vivo or in the photobiology lab. The purpose of this study was to characterize the response of vitamin D metabolites following a 30-min bout of sun exposure (15-min each to the dorsal and ventral sides) at close to solar noon in younger and older adults. Methods: 30 healthy individuals with skin type II/III were recruited; a younger cohort, aged 20–37 (n = 18) and an older cohort (n = 12), age 51–69 years. Exposure was at outer limits of sensible sun exposure designed to enhance vitamin D synthesis without increasing risk of photo ageing and non-melanoma skin cancer. Serum D(3) concentration was measured at baseline, 24, 48 and 72 h post-exposure. Serum 25(OH)D was measured at baseline and 72 h post-exposure plus 168 h post-exposure in the older cohort. Results: D(3) increased in response to sun exposure (time effect; p = 0.002) with a trend for a difference in D(3) between cohorts (time*group; p = 0.09). By regression modeling of continuous data, age accounted for 20% of the variation in D(3) production. D(3) production decreased by 13% per decade. Despite changes in D(3), however, serum 25(OH)D did not change from baseline to 72 or 168 h post exposure (p > 0.10). Conclusions: Serum D(3) concentration increased significantly in response to outdoor sun exposure in younger and older adults. While ageing may dampen cutaneous synthesis, sunlight exposure is still a significant source of vitamin D(3).