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Longevity of daily oral vitamin D3 supplementation: Differences in 25OHD and 24,25(OH)2D observed 2 years after cessation of a 1-year randomised controlled trial (VICtORy RECALL)

dc.contributor.authorMacdonald, H.M.en
dc.contributor.authorGryka-MacPhail, Annaen
dc.contributor.authorTang, J. C. Y.en
dc.contributor.authorAucott, L. S.en
dc.contributor.authorFraser, W. D.en
dc.contributor.authorWood, A. D.en
dc.date.accessioned2022-03-30T13:17:00Z
dc.date.available2022-03-30T13:17:00Z
dc.date.issued2017-09-15
dc.descriptionItem not available in this repository.en
dc.description.abstractSummary To determine how long vitamin D lasts after supplementation ceases, the marker of status was measured 2 and 3 years after a 1-year trial. Compared to placebo, the proportion of vitamin D-deficient women was still lower, if they had taken daily vitamin D3, after 2 years, indicating its longevity. Introduction The purpose of this study was to determine longevity of vitamin D status following cessation of vitamin D3 supplementation, 2 and 3 years after a 1-year randomised, double-blind placebo controlled trial and to investigate possible predictive factors. Methods Caucasian non-smoking postmenopausal women randomised to ViCtORY (2009–2010), who had not taken vitamin D supplements since the trial ended, were invited to attend follow-up visits. Total 25-hydroxyvitamin D (25OHD) and 24,25-dihydroxyvitamin D (24,25OH2D) were measured by dual tandem mass spectrometry of serum samples following removal of protein and de-lipidation; the original randomised controlled trial (RCT) samples were re-analysed simultaneously. Vitamin D-binding protein (VDBP) was measured by monoclonal immunoassay. Results In March 2012 and March 2013, 159 women (mean (SD) age 67.6 (2.1) years) re-attended, equally distributed between the original treatment groups: daily vitamin D3 (400 IU, 1000 IU) and placebo. One month after the RCT ended (March 2010), the proportion of women in placebo, 400 IU and 1000 IU vitamin D3 groups, respectively, with 25OHD < 25 nmol/L was 15, 0 and 0 (chi-square p < 0.001, n = 46, 44, 54). After 2 years (March 2012), it was 22, 4 and 4% (p = 0.002, n = 50, 48, 57); after 3 years, it was 23, 13 and 15% (p = 0.429, n = 48, 45, 52). The respective proportions of women with 24,25OH2D < 2.2 nmol/L were 50, 2 and 2% (1 month, p < 0.001, n = 46, 44, 54); 42, 33 and 12% (2 years, p = 0.002, n = 50, 48, 57); and 45, 27 and 29% (3 years, p = 0.138, n = 47, 45, 51). VDBP was a predictor of circulating 25OHD longevity (beta for VDBP in μg/mL 0.736; 95% CI 0.216–1.255, p = 0.006) but not 24,25OH2D. Conclusion Four hundred international units or 1000 IU of daily vitamin D3 showed benefits over placebo 2 years after supplementation ceased in keeping 25OHD > 25 nmol/L.en
dc.description.ispublishedpub
dc.description.sponsorshipThis work was funded partly by the UK Food Standards Agency and the Department of Health.en
dc.description.statuspub
dc.description.urihttps://doi.org/10.1007/s00198-017-4201-2en
dc.description.volume28en
dc.format.extent3361-3372en
dc.identifier.citationMacdonald, H.M., Gryka-MacPhail, A., Tang, J.C.Y., Aucott, L.S., Fraser, W.D. and Wood, A.D. (2017) ‘Longevity of daily oral vitamin D3 supplementation: Differences in 25OHD and 24,25(OH)2D observed 2 years after cessation of a 1-year randomised controlled trial (VICtORy RECALL)’, Osteoporosis International, 28, pp. 3361-3372.en
dc.identifier.issn1433-2965en
dc.identifier.issn0937-941X
dc.identifier.urihttps://doi.org/10.1007/s00198-017-4201-2
dc.identifier.urihttps://eresearch.qmu.ac.uk/handle/20.500.12289/11970
dc.language.isoenen
dc.publisherInternational Osteoporosis Foundationen
dc.relation.ispartofOsteoporosis Internationalen
dc.subject24,25-Dihydroxyvitamin Den
dc.subject25-Hydroxyvitamin Den
dc.subjectDaily Vitamin Den
dc.subjectLongevityen
dc.subjectPostmenopausal Womenen
dc.subjectRCTen
dc.titleLongevity of daily oral vitamin D3 supplementation: Differences in 25OHD and 24,25(OH)2D observed 2 years after cessation of a 1-year randomised controlled trial (VICtORy RECALL)en
dc.typeArticleen
dcterms.accessRightsnone
dcterms.dateAccepted2017-08-17
qmu.authorGryka-MacPhail, Annaen
refterms.accessExceptionNAen
refterms.depositExceptionNAen
refterms.panelUnspecifieden
refterms.technicalExceptionNAen
refterms.versionNAen
rioxxterms.publicationdate2017-09-15
rioxxterms.typeJournal Article/Reviewen

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