Graeme S. MacLennan
Long-term follow-up for mortality and cancer in a randomized placebo-controlled trial of vitamin D3 and/or calcium (RECORD Trial)
MacLennan, Graeme S.; McDonald, Alison M.; Grant, Adrian M.; Khaw, K. T.; Eastell, R.; Marsh, D.; McDonald, GM; Pant, Puspa Raj; Grant, Adrian; Avenell, Alison; Jenkinson, David J.; McPherson, Gladys C.; Campbell, Marion K.; Anderson, Frazer H.; Cooper, Cyrus; Francis, Roger M.; Gillespie, William J.; Robinson, C. Michael; Torgerson, David J.; Wallace, W. Angus
Authors
Alison M. McDonald
Adrian M. Grant
K. T. Khaw
R. Eastell
D. Marsh
GM McDonald
Dr Puspa Pant Puspa.Pant@uwe.ac.uk
Research Fellow (SAFETRIP Nepal)
Adrian Grant
Alison Avenell
David J. Jenkinson
Gladys C. McPherson
Marion K. Campbell
Frazer H. Anderson
Cyrus Cooper
Roger M. Francis
William J. Gillespie
C. Michael Robinson
David J. Torgerson
W. Angus Wallace
Abstract
Context: Vitamin D or calcium supplementation may have effects on vascular disease and cancer. Objective: Our objective was to investigate whether vitamin D or calcium supplementation affects mortality, vascular disease, and cancer in older people. Design and Setting: The study included long-term follow-up of participants in a two by two factorial, randomized controlled trial from 21 orthopedic centers in the United Kingdom. Participants: Participants were 5292 people (85% women) aged at least 70 yr with previous low-trauma fracture. Interventions: Participants were randomly allocated to daily vitamin D 3 (800 IU), calcium (1000 mg), both, or placebo for 24-62 months, with a follow-up of 3 yr after intervention. Main Outcome Measures: All-cause mortality, vascular disease mortality, cancer mortality, and cancer incidence were evaluated. Results: In intention-to-treat analyses, mortality [hazard ratio (HR) = 0.93; 95% confidence interval (CI) = 0.85-1.02], vascular disease mortality (HR = 0.91; 95% CI = 0.79-1.05), cancer mortality (HR = 0.85; 95% CI = 0.68-1.06), and cancer incidence (HR = 1.07; 95% CI = 0.92-1.25) did not differ significantly between participants allocated vitamin D and those not. All-cause mortality (HR = 1.03; 95% CI = 0.94-1.13), vascular disease mortality (HR = 1.07; 95% CI = 0.92-1.24), cancer mortality (HR = 1.13; 95% CI = 0.91-1.40), and cancer incidence (HR = 1.06; 95% CI = 0.91-1.23) also did not differ significantly between participants allocated calcium and those not. In a post hoc statistical analysis adjusting for compliance, thus with fewer participants, trends for reduced mortality with vitamin D and increased mortality with calcium were accentuated, although all results remain nonsignificant. Conclusions: Daily vitamin D or calcium supplementation did not affect mortality, vascular disease, cancer mortality, or cancer incidence. Copyright © 2012 by The Endocrine Society.
Journal Article Type | Article |
---|---|
Publication Date | Feb 1, 2012 |
Journal | Journal of Clinical Endocrinology and Metabolism |
Print ISSN | 0021-972X |
Electronic ISSN | 1945-7197 |
Publisher | Oxford University Press (OUP) |
Peer Reviewed | Peer Reviewed |
Volume | 97 |
Issue | 2 |
Pages | 614-622 |
DOI | https://doi.org/10.1210/jc.2011-1309 |
Keywords | cancer, randomized controlled trial, RCT, vitamin D3, calcium |
Public URL | https://uwe-repository.worktribe.com/output/957478 |
Publisher URL | http://dx.doi.org/10.1210/jc.2011-1309 |
Additional Information | Corporate Creators : RECORD Trial Group |
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