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Meta-Analysis
. 2022 May 5;17(1):74.
doi: 10.1007/s11657-022-01071-3.

Overview of the clinical efficacy and safety of eldecalcitol for the treatment of osteoporosis

Affiliations
Meta-Analysis

Overview of the clinical efficacy and safety of eldecalcitol for the treatment of osteoporosis

Lijia Cui et al. Arch Osteoporos. .

Abstract

Eldecalcitol (ELD) is a new oral analog of the active form of vitamin D with anti-resorptive properties. We conducted a meta-analysis to investigate the efficacy and safety of ELD in osteoporosis. Compared with alfacalcidol, ELD significantly lowered vertebral facture risk, increased bone mineral density, but also had a higher risk of hypercalciuria.

Purpose: This study aimed to investigate the efficacy and safety of eldecalcitol (ELD) in osteoporosis by examining fracture rates, bone mineral density (BMD), bone turnover markers, and adverse events as outcomes.

Methods: PubMed, EMBASE, and Cochrane Library were searched up to July 20, 2020, to identify eligible randomized controlled trials. The odds ratio (OR) or weighted mean difference (WMD) with 95% confidence interval was calculated by the random-effects model.

Results: ELD significantly increased lumbar BMD (WMD: 2.80; 95% CI: 1.60, 4.00; P < 0.001, 2 studies involved), total hip BMD (WMD: 2.11; 95% CI: 0.68, 3.55; P = 0.004, 2 studies involved), and femoral neck BMD (WMD: 1.78; 95% CI: 0.76, 2.79; P = 0.001, 1 study involved) compared with alfacalcidol. Moreover, ELD caused a significantly lower rate of vertebral fracture (OR: 0.52; 95% CI: 0.29-0.95; P = 0.034, 2 studies involved) than alfacalcidol, but did not lower the rate of non-vertebral facture (OR: 0.44; 95% CI: 0.06-3.05; P = 0.405, 2 studies involved) compared with alfacalcidol. ELD significantly reduced the percentage change in bone-specific alkaline phosphatase (WMD: - 15.40; 95% CI: - 20.30, - 10.60; P < 0.001, 1 study involved) and serum type I collagen C-telopeptide (WMD: - 38.50; 95% CI: - 50.00, - 27.10; P < 0.001, 1 study involved) as compared with alfacalcidol. ELD was also associated with higher risk of hypercalciuria compared with alfacalcidol (OR: 1.64; 95% CI: 1.22, 2.20; P = 0.001, 2 studies involved).

Conclusions: This systematic review indicated that ELD was superior than alfacalcidol for improving vertebral fracture risk and BMD. Further large-scale trials should be conducted to verify the long-term effects and safety of ELD in osteoporosis.

Prospero registration number: CRD42020147518.

Keywords: Bone mineral density; Eldecalcitol; Fracture; Osteoporosis; Systematic review.

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Conflict of interest statement

None.

Figures

Fig. 1
Fig. 1
Flow diagram of selection process of the studies
Fig. 2
Fig. 2
Risk-of-bias assessments for included trials
Fig. 3
Fig. 3
Random-effects meta-analysis of eldecalcitol compared with other active vitamin D on bone mineral density at various sites. BMD: bone mineral density; WMD: weighted mean difference; 95% CI: 95% confidence interval
Fig. 4
Fig. 4
Random-effects meta-analysis of eldecalcitol compared with other active vitamin D on fracture rates. OR: odds ratio; 95% CI: 95% confidence interval

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