Eldecalcitol is superior to alfacalcidol in maintaining bone mineral density in glucocorticoid-induced osteoporosis patients (e-GLORIA)

被引:25
作者
Matsumoto, Toshio [1 ]
Yamamoto, Kazuhiko [2 ]
Takeuchi, Tsutomu [3 ]
Tanaka, Yoshiya [4 ]
Tanaka, Sakae [5 ]
Nakano, Tetsuo [6 ]
Ito, Masako [7 ]
Tomomitsu, Tatsushi [8 ]
Hirakawa, Akihiro [9 ]
Soen, Satoshi [10 ]
机构
[1] Tokushima Univ, Fujii Mem Inst Med Sci, Tokushima 7708530, Japan
[2] RIKEN Ctr Integrat Med Sci, Lab Autoimmune Dis, Yokohama, Kanagawa, Japan
[3] Keio Univ, Sch Med, Div Rheumatol, Dept Internal Med, Tokyo, Japan
[4] Univ Occupat & Environm Hlth, Sch Med, Dept Internal Med 1, Kitakyushu, Fukuoka, Japan
[5] Univ Tokyo, Dept Orthopaed Surg, Grad Sch Med, Tokyo, Japan
[6] Tamana Cent Hosp, Tamana, Kumamoto, Japan
[7] Open Univ Japan, Nagasaki, Japan
[8] Kawasaki Med Sch, Dept Radiol, Kurashiki, Okayama, Japan
[9] Univ Tokyo, Dept Biostat & Bioinformat, Grad Sch Med, Tokyo, Japan
[10] Kindai Univ, Dept Orthopaed Surg & Rheumatol, Nara Hosp, Ikoma, Nara, Japan
关键词
Active vitamin D; Secondary osteoporosis; Fracture; Alfacalcidol; CORTICOSTEROID-INDUCED OSTEOPOROSIS; DOUBLE-BLIND; VERTEBRAL FRACTURE; VITAMIN-D; RISEDRONATE; ALENDRONATE; PREVENTION; RISK;
D O I
10.1007/s00774-020-01091-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Eldecalcitol increases bone mineral density (BMD) and reduces vertebral fracture in patients with primary osteoporosis. However, the effect of eldecalcitol on BMD and fracture in glucocorticoid-induced osteoporosis (GIO) patients is unknown. This study was undertaken to compare the effect of eldecalcitol on BMD and fracture with that of alfacalcidol in GIO patients. Materials and methods A randomized, open-label, parallel group study was conducted to identify the effectiveness and safety of monotherapy with 0.75 mu g eldecalcitol compared with 1.0 mu g alfacalcidol in GIO patients. Results Lumbar spine BMD increased with eldecalcitol, but decreased with alfacalcidol at 12 and 24 months (between group difference 1.29%, p < 0.01, and 1.10%, p < 0.05, respectively). Total hip and femoral neck BMD were maintained until 24 months by eldecalcitol, but decreased by alfacalcidol (between group difference 0.97%, p < 0.05 and 1.22%, p < 0.05, respectively). Both bone formation and resorption markers were more strongly suppressed by eldecalcitol than by alfacalcidol. Eldecalcitol showed better effect on BMD than alfacalcidol in patients with no prevalent fracture and BMD > 70% of the young adult mean, and with <= 3 months of previous glucocorticoid treatment. No significant difference in the incidence of vertebral fracture was found, and the incidence of adverse events was similar between the two groups. Conclusions Eldecalcitol was more effective than alfacalcidol in maintaining BMD in GIO patients. Because eldecalcitol was effective in patients with no or short-term previous glucocorticoid treatment, as well as those without prevalent fracture or low BMD, eldecalcitol can be a good candidate for primary prevention of GIO.
引用
收藏
页码:522 / 532
页数:11
相关论文
共 20 条
  • [1] Adachi JD, 2001, ARTHRITIS RHEUM-US, V44, P202, DOI 10.1002/1529-0131(200101)44:1<202::AID-ANR27>3.0.CO
  • [2] 2-W
  • [3] Glucocorticoid-induced osteoporosis
    Clowes, JA
    Peel, N
    Eastell, R
    [J]. CURRENT OPINION IN RHEUMATOLOGY, 2001, 13 (04) : 326 - 332
  • [4] Eldecalcitol increases bone mineral density in Chinese osteoporotic patients without vitamin D or calcium supplementation
    Jiang, Yan
    Tang, Hai
    Ma, Xinlong
    Cheng, Qun
    Lin, Hua
    Jin, Xiaolan
    Zhang, Zhenlin
    Yu, Wei
    He, Shuli
    Kobayashi, Tsuyoshi
    Uehara, Satomi
    Matsumoto, Toshio
    Xia, Weibo
    [J]. JOURNAL OF BONE AND MINERAL METABOLISM, 2019, 37 (06) : 1036 - 1047
  • [5] Kanis JA, 2007, HEALTH TECHNOL ASSES, V11, P1
  • [6] The science and therapy of glucocorticoid-induced bone loss
    Lane, NE
    Lukert, B
    [J]. ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1998, 27 (02) : 465 - +
  • [7] Which is the preferred site for bone mineral density monitoring as an indicator of treatment-related anti-fracture effect in routine clinical practice? A registry-based cohort study
    Leslie, W. D.
    Martineau, P.
    Bryanton, M.
    Lix, L. M.
    [J]. OSTEOPOROSIS INTERNATIONAL, 2019, 30 (07) : 1445 - 1453
  • [8] A new active vitamin D, ED-71, increases bone mass in osteoporotic patients under vitamin D supplementation: A randomized, double-blind, placebo-controlled clinical trial
    Matsumoto, T
    Miki, T
    Hagino, H
    Sugimoto, T
    Okamoto, S
    Hirota, T
    Tanigawara, Y
    Hayashi, Y
    Fukunaga, M
    Shiraki, M
    Nakamura, T
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (09) : 5031 - 5036
  • [9] A new active vitamin D3 analog, eldecalcitol, prevents the risk of osteoporotic fractures - A randomized, active comparator, double-blind study
    Matsumoto, Toshio
    Ito, Masako
    Hayashi, Yasufumi
    Hirota, Takako
    Tanigawara, Yusuke
    Sone, Teruki
    Fukunaga, Masao
    Shiraki, Masataka
    Nakamura, Toshitaka
    [J]. BONE, 2011, 49 (04) : 605 - 612
  • [10] Zoledronic acid and risedronate in the prevention and treatment of glucocorticoid-induced osteoporosis (HORIZON): a multicentre, double-blind, double-dummy, randomised controlled trial
    Reid, David M.
    Devogelaer, Jean-Pierre
    Saag, Kenneth
    Roux, Christian
    Lau, Chak-Sing
    Reginster, Jean-Yves
    Papanastasiou, Philemon
    Ferreira, Alberto
    Hartl, Florian
    Fashola, Taiwo
    Mesenbrink, Peter
    Sambrook, Philip N.
    [J]. LANCET, 2009, 373 (9671) : 1253 - 1263