Safety of High-Dose Vitamin D Supplementation: Secondary Analysis of a Randomized Controlled Trial

被引:48
作者
Billington, Emma O. [1 ]
Burt, Lauren A. [1 ]
Rose, Marianne S. [2 ]
Davison, Erin M. [1 ]
Gaudet, Sharon [1 ]
Kan, Michelle [1 ]
Boyd, Steven K. [1 ]
Hanley, David A. [1 ]
机构
[1] Univ Calgary, Cumming Sch Med, McCaig Inst Bone & Joint Hlth, Calgary, AB, Canada
[2] Alberta Hlth Serv, Res Facilitat, Calgary, AB, Canada
关键词
Vitamin D; cholecalciferol; dietary supplements; hypercalcemia; hypercalciuria; adverse drug events; DOUBLE-BLIND; OLDER WOMEN; RISK; CALCIUM; FALLS; OSTEOPOROSIS; PREVENTION; MANAGEMENT; FRACTURES; SOCIETY;
D O I
10.1210/clinem/dgz212
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: More than 3% of adults report vitamin D intakes of 4000 IU/day or more, but the safety of this practice is unknown. Objective: The objective of this work is to establish whether vitamin D doses up to 10 000 IU/day are safe and well tolerated. Design: The Calgary Vitamin D Study was a 3-year, double-blind, randomized controlled trial. Setting: A single-center study was conducted at the University of Calgary, Canada. Participants: Participants included healthy adults (n = 373) ages 55 to 70 years with serum 25-hydroxyvitamin D 30 to 125 nmol/L. Interventions: Participants were randomly assigned 1:1:1 to vitamin D 3 400, 40 000, or 10 000 IU/day. Calcium supplementation was initiated if dietary calcium intake was less than 1200 mg/day. Main Outcome Measures: In these prespecified secondary analyses, changes in serum 25-hydroxyvitamin D, calcium, creatinine, 24-hour urine calcium excretion, and incidence of adverse events were assessed. Between-group differences in adverse events were examined using incident rate differences and logistic regression. Results: Of 373 participants (400: 124, 4000: 125, 10 000: 124), 49% were male, mean (SD) age was 64 (4) years, and 25-hydroxyvitamin D 78.0 (19.5) nmol/L. Serum calcium, creatinine, and 24-hour urine calcium excretion did not differ between treatments. Mild hypercalcemia (2.56-2.64 mmol/L) occurred in 15 (4%) participants (400: 0%, 4000: 3%, 10 000: 9%, P =.002); all cases resolved on repeat testing. Hypercalciuria occurred in 87 (23%) participants (400: 17%, 4000: 22%, 10 000: 31%, P =.01). Clinical adverse events were experienced by 365 (97.9%) participants and were balanced across treatment arms. Conclusions: The safety profile of vitamin D supplementation is similar for doses of 400, 4000, and 10 000 IU/day. Hypercalciuria was common and occurred more frequently with higher doses. Hypercalcemia occurred more frequently with higher doses but was rare, mild, and transient.
引用
收藏
页码:1261 / 1273
页数:13
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