Randomized controlled trials of vitamin D and cancer incidence: A modeling study.

Although geographic ecological studies and observational studies find that ultraviolet B exposure and 25-hydroxyvitamin D [25(OH)D] concentrations are inversely correlated with 15-20 types of cancer, few randomized controlled trials (RCTs) of vitamin D support those findings. The poor design of some...

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Main Authors: William B Grant, Barbara J Boucher
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5411066?pdf=render
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spelling doaj-c7184d68956a4adeb6082a4e6fb15a272020-11-24T21:50:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01125e017644810.1371/journal.pone.0176448Randomized controlled trials of vitamin D and cancer incidence: A modeling study.William B GrantBarbara J BoucherAlthough geographic ecological studies and observational studies find that ultraviolet B exposure and 25-hydroxyvitamin D [25(OH)D] concentrations are inversely correlated with 15-20 types of cancer, few randomized controlled trials (RCTs) of vitamin D support those findings. The poor design of some RCTs may account for that lack of support. Most vitamin D RCTs to date have considered the vitamin D dose, rather than initial, final, or changes in, serum 25(OH)D concentrations. Here a model is developed for use in designing and analyzing vitamin D RCTs with application to cancer incidence. The input variables of the model are vitamin D dose, baseline and achieved 25(OH)D concentrations, known rates of cancer for the population, and numbers of participants for the treatment and placebo arms is estimated-vitamin D dosage and numbers of participants are varied to achieve desired hazard ratio significance, using information from two vitamin D RCTs on cancer incidence conducted in Nebraska with good agreement between the model estimates and reported hazard ratios. Further improvements to the conduct of vitamin D RCTs would be to start the trial with a moderate bolus dose to achieve the desired 25(OH)D concentrations, and bloodspot 25(OH)D assay use in summer and winter annually to monitor seasonal and long-term changes in 25(OH)D concentration and compliance, and to allow dosage adjustment for achievement of desired vitamin D status.http://europepmc.org/articles/PMC5411066?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author William B Grant
Barbara J Boucher
spellingShingle William B Grant
Barbara J Boucher
Randomized controlled trials of vitamin D and cancer incidence: A modeling study.
PLoS ONE
author_facet William B Grant
Barbara J Boucher
author_sort William B Grant
title Randomized controlled trials of vitamin D and cancer incidence: A modeling study.
title_short Randomized controlled trials of vitamin D and cancer incidence: A modeling study.
title_full Randomized controlled trials of vitamin D and cancer incidence: A modeling study.
title_fullStr Randomized controlled trials of vitamin D and cancer incidence: A modeling study.
title_full_unstemmed Randomized controlled trials of vitamin D and cancer incidence: A modeling study.
title_sort randomized controlled trials of vitamin d and cancer incidence: a modeling study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Although geographic ecological studies and observational studies find that ultraviolet B exposure and 25-hydroxyvitamin D [25(OH)D] concentrations are inversely correlated with 15-20 types of cancer, few randomized controlled trials (RCTs) of vitamin D support those findings. The poor design of some RCTs may account for that lack of support. Most vitamin D RCTs to date have considered the vitamin D dose, rather than initial, final, or changes in, serum 25(OH)D concentrations. Here a model is developed for use in designing and analyzing vitamin D RCTs with application to cancer incidence. The input variables of the model are vitamin D dose, baseline and achieved 25(OH)D concentrations, known rates of cancer for the population, and numbers of participants for the treatment and placebo arms is estimated-vitamin D dosage and numbers of participants are varied to achieve desired hazard ratio significance, using information from two vitamin D RCTs on cancer incidence conducted in Nebraska with good agreement between the model estimates and reported hazard ratios. Further improvements to the conduct of vitamin D RCTs would be to start the trial with a moderate bolus dose to achieve the desired 25(OH)D concentrations, and bloodspot 25(OH)D assay use in summer and winter annually to monitor seasonal and long-term changes in 25(OH)D concentration and compliance, and to allow dosage adjustment for achievement of desired vitamin D status.
url http://europepmc.org/articles/PMC5411066?pdf=render
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