Effects of risedronate alone or combined with vitamin K2 on serum undercarboxylated osteocalcin and osteocalcin levels in postmenopausal osteoporosis
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  • 作者:Yuji Kasukawa (1)
    Naohisa Miyakoshi (1)
    Toshihito Ebina (2)
    Toshiaki Aizawa (2)
    Michio Hongo (1)
    Koji Nozaka (1)
    Yoshinori Ishikawa (1)
    Hidetomo Saito (1)
    Shuichi Chida (1)
    Yoichi Shimada (1)
  • 关键词:Risedronate ; Vitamin K2 ; Undercarboxylated osteocalcin (ucOC) ; Osteocalcin ; Vertebral fracture
  • 刊名:Journal of Bone and Mineral Metabolism
  • 出版年:2014
  • 出版时间:May 2014
  • 年:2014
  • 卷:32
  • 期:3
  • 页码:290-297
  • 全文大小:
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  • 作者单位:Yuji Kasukawa (1)
    Naohisa Miyakoshi (1)
    Toshihito Ebina (2)
    Toshiaki Aizawa (2)
    Michio Hongo (1)
    Koji Nozaka (1)
    Yoshinori Ishikawa (1)
    Hidetomo Saito (1)
    Shuichi Chida (1)
    Yoichi Shimada (1)

    1. Department of Orthopedic Surgery, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita, 010-8543, Japan
    2. Department of Orthopedic Surgery, Kakunodate General Hospital, Senboku, 010-0394, Japan
  • ISSN:1435-5604
文摘
Risedronate decreases osteoporotic fracture incidence; however, its effects remain unclear in elderly osteoporotic patients. Vitamin K mediates carboxylation of osteocalcin (OC), and high undercarboxylated osteocalcin (ucOC) levels indicate vitamin K deficiency and increased osteoporotic fracture risk. We aimed to evaluate the effects of risedronate alone or combined with vitamin K2 on serum ucOC, OC, and incidence of vertebral fractures in elderly osteoporotic patients. A total of 101 women with postmenopausal osteoporosis aged >60?years were randomly stratified into two groups—R group (n?=?51), treated with risedronate alone; and R?+?K group (n?=?50), treated with risedronate and vitamin K2. Serum ucOC, OC and incidence of vertebral fractures were evaluated before treatment and at 6 and 12?months post-treatment. Decreased ucOC rates at 6 and 12?months were not significant between groups. However, at 6 and 12?months, decreased OC rates in the R group (p?<?0.01 and 0.05, respectively) were significantly higher than in the R?+?K group, and ucOC/OC change rates in the R group (p?<?0.05 and 0.001, respectively) were significantly lower than in the R?+?K group. Vertebral fracture incidence was not significantly different between the groups at 6 and 12?months. ucOC levels in patients with incident vertebral fractures were significantly higher than in patients without incident vertebral fractures in the R group at 6?months (p?<?0.05). Although no significant difference was observed for ucOC decrease rate and incidence of vertebral fractures between treatments, ucOC levels in patients with incident vertebral fractures were significantly greater than in patients without when using risedronate alone.

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