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Randomized Controlled Trial
. 2008 Jun;87(6):1945-51.
doi: 10.1093/ajcn/87.6.1945.

Effect of calcium supplementation on fracture risk: a double-blind randomized controlled trial

Heike A Bischoff-Ferrari  1 , Judy R Rees, Maria V Grau, Elizabeth Barry, Jiang Gui, John A Baron
Affiliations
Randomized Controlled Trial

Effect of calcium supplementation on fracture risk: a double-blind randomized controlled trial

Heike A Bischoff-Ferrari et al. Am J Clin Nutr. 2008 Jun.

Abstract

Background: The effect of supplementation with calcium alone on risk fractures in a healthy population is not clear.

Objective: The objective was to determine whether 4 y of calcium supplementation would reduce the fracture risk during treatment and subsequent follow-up in a randomized placebo-controlled trial.

Design: The participants were aged <80 y at study entry (mean age: 61 y), were generally healthy, and had a recent diagnosis of colorectal adenoma. A total of 930 participants (72% men; mean age: 61 y) were randomly assigned to receive 4 y of treatment with 3 g CaCO(3) (1200 mg elemental Ca) daily or placebo and were followed for a mean of 10.8 y. The primary outcomes of this analysis were all fractures and minimal trauma fractures (caused by a fall from standing height or lower while sitting, standing, or walking).

Results: There were 46 fractures (15 from minimal trauma) in 464 participants in the calcium group and 54 (29 from minimal trauma) in 466 participants in the placebo group. The overall risk of fracture differed significantly between groups during the treatment phase [hazard ratio (HR): 0.28; 95% CI: 0.09, 0.85], but not during the subsequent posttreatment follow-up (HR: 1.10; 95% CI: 0.71, 1.69). Minimal trauma fractures were also less frequent in the calcium group during treatment (HR: 0; 95% CI: 0, 0.50).

Conclusion: Calcium supplementation reduced the risk of all fractures and of minimal trauma fractures among healthy individuals. The benefit appeared to dissipate after treatment was stopped. This trial was registered at clinicaltrials.gov as NCT00153816.

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Conflict of interest statement

The authors’ responsibilities were as follows—HAB-F: had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis; HAB-F, JRR, and JAB: study concept and design; JAB: administrative, technical, and material support; HAB-F and JAB: obtained funding; HAB-F, JRR, MVG, and JAB: acquisition of data; and HAB-F, JRR, and MVG: conducted the statistical analysis. All authors drafted the manuscript, critically revised the manuscript for important intellectual content, and analyzed and interpreted the data. No sponsors participated in the design and conduct of the study; in the collection, analysis, and interpretation of the data; or in the preparation, review, or approval of the manuscript. No conflicts of interest were declared.

Figures

FIGURE 1
FIGURE 1
Numbers of subjects studied and dropouts during the intervention and observational phases of the trial, by treatment allocation.
FIGURE 2
FIGURE 2
Use of calcium supplements in the observational follow-up after the treatment phase. Of 821 individuals followed after the treatment phase, 48% reported using calcium supplements regularly for ≥1 y, and 26% did so for at least half of the follow-up years for which questionnaire data were available. Personal use of calcium supplements during the observational phase was similar between the randomized groups (Students t test: P = 0.68).
FIGURE 3
FIGURE 3
Cumulative incidence of minimal trauma fractures, by treatment group. The unadjusted hazard ratio for the comparison of calcium with placebo was 0.52 (95% CI: 0.28, 0.97; P = 0.04) across the total follow-up, including both the intervention and the observational phases of the study. The odds ratio during the treatment phase was 0.00 (95% CI: 0.00, 0.50); during the posttreatment phase, the unadjusted hazard ratio was 0.78 (95% CI: 0.40, 1.52).
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