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A new active vitamin D3 analog, eldecalcitol, prevents the risk of osteoporotic fractures--a randomized, active comparator, double-blind study
Authors:Matsumoto Toshio  Ito Masako  Hayashi Yasufumi  Hirota Takako  Tanigawara Yusuke  Sone Teruki  Fukunaga Masao  Shiraki Masataka  Nakamura Toshitaka
Affiliation:aUniversity of Tokushima Graduate School of Medical Sciences, Tokushima 770-8503, Japan;bNagasaki University, Nagasaki 852-8501, Japan;cTokyo Metropolitan Rehabilitation Hospital, Tokyo 131-0034, Japan;dKyoto Koka Women's University, Kyoto 615-0882, Japan;eKeio University, Tokyo 160-8582, Japan;fKawasaki Medical School, Okayama 701-0192, Japan;gResearch Institute and Practice for Involutional Diseases, Nagano 399-8101, Japan;hUniversity of Occupational and Environmental Health, Fukuoka 807-8555, Japan
Abstract:

Background

Eldecalcitol is an analog of 1,25-dihydroxyvitamin D3 that improves bone mineral density; however, the effect of eldecalcitol on the risk of fractures is unclear. The objective of this study is to examine whether eldecalcitol is superior to alfacalcidol in preventing osteoporotic fractures. This trial is registered with ClinicalTrials.gov, number NCT00144456.

Methods and results

This 3 year randomized, double-blind, active comparator, superiority trial tested the efficacy of daily oral 0.75 μg eldecalcitol versus 1.0 μg alfacalcidol for prevention of osteoporotic fractures. 1054 osteoporotic patients 46 to 92 years old were randomly assigned 1:1 to receive eldecalcitol (n = 528) or alfacalcidol (n = 526). Patients were stratified by study site and serum 25-hydroxyvitamin D level. Patients with low serum 25-hydroxyvitamin D levels (< 50 nmol/L) were supplemented with 400 IU/day vitamin D3. Primary end point was incident vertebral fractures. Secondary end points included any non-vertebral fractures and change in bone mineral density and bone turnover markers. Compared with the alfacalcidol group, the incidence of vertebral fractures was lower in eldecalcitol group after 36 months of treatment (13.4 vs. 17.5%; hazard ratio, 0.74; predefined 90% confidence interval [CI], 0.56–0.97). Eldecalcitol reduced turnover markers and increased bone mineral density more strongly than alfacalcidol. Eldecalcitol reduced the incidence of three major non-vertebral fractures, which was due to a marked reduction in wrist fractures by a post-hoc analysis (1.1 vs. 3.6%; hazard ratio, 0.29; 95% CI, 0.11–0.77). Among the adverse events, the incidence of increase in serum and urinary calcium was higher in the eldecalcitol group, without any difference in glomerular filtration rate between the two groups.

Conclusions

Eldecalcitol is more efficacious than alfacalcidol in preventing vertebral and wrist fractures in osteoporotic patients with vitamin D sufficiency, with a safety profile similar to alfacalcidol.
Keywords:Osteoporosis   Vertebral fracture   Wrist fracture   Bone mineral density   Active vitamin D
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