Calcitriol and alendronate combination treatment in menopausal women with low bone mass.

N Malavolta, M Zanardi, M Veronesi, C Ripamonti, S Gnudi
{"title":"Calcitriol and alendronate combination treatment in menopausal women with low bone mass.","authors":"N Malavolta,&nbsp;M Zanardi,&nbsp;M Veronesi,&nbsp;C Ripamonti,&nbsp;S Gnudi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Serum calcitriol levels decrease with advancing age in relation to reduced dietary intake or poor intestinal absorption of vitamin D. These decreased levels affect the development of senile osteopenia, which can be effectively prevented by the administration of alendronate and calcium. To evaluate the effect of a combined treatment with alendronate and calcitriol on bone mineral density (BMD), we followed 152 osteopenic postmenopausal women, aged 55-75 years, for 9 months. They were divided into three groups. The first group was treated every other day with 0.25 microgram of synthetic 1,25-dihydroxyvitamin D3 plus 10 mg alendronate. The second group received the same dose of alendronate plus calcium (500 mg/day). The third group received only calcium (500 mg/day). BMD measurements were made at the level of the lumbar spine and the femoral neck. At the beginning and at the end of the period of treatment the same biochemical analyses of bone metabolism were made. There were no significant differences in the baseline values of the three groups in the biological parameters. Alendronate plus calcium treatment led to a significant reduction in total alkaline phosphatase and hydroxy prolinuria as well as to a significant increase in lumbar and femoral bone density. The same changes were observed in the group treated with alendronate plus calcitriol except that femoral BMD did not significantly improve. These results show that continuous treatment for 9 months with calcitriol or calcium in combination with alendronate significantly increases both vertebral and femoral neck density (from 3.8% to 4.5% and from 0.61% to 2.36% respectively) in osteopenic postmenopausal women. The effects of both combinations on bone mass are clearly greater than those achieved by calcium monotherapy.</p>","PeriodicalId":14404,"journal":{"name":"International journal of tissue reactions","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1999-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of tissue reactions","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Serum calcitriol levels decrease with advancing age in relation to reduced dietary intake or poor intestinal absorption of vitamin D. These decreased levels affect the development of senile osteopenia, which can be effectively prevented by the administration of alendronate and calcium. To evaluate the effect of a combined treatment with alendronate and calcitriol on bone mineral density (BMD), we followed 152 osteopenic postmenopausal women, aged 55-75 years, for 9 months. They were divided into three groups. The first group was treated every other day with 0.25 microgram of synthetic 1,25-dihydroxyvitamin D3 plus 10 mg alendronate. The second group received the same dose of alendronate plus calcium (500 mg/day). The third group received only calcium (500 mg/day). BMD measurements were made at the level of the lumbar spine and the femoral neck. At the beginning and at the end of the period of treatment the same biochemical analyses of bone metabolism were made. There were no significant differences in the baseline values of the three groups in the biological parameters. Alendronate plus calcium treatment led to a significant reduction in total alkaline phosphatase and hydroxy prolinuria as well as to a significant increase in lumbar and femoral bone density. The same changes were observed in the group treated with alendronate plus calcitriol except that femoral BMD did not significantly improve. These results show that continuous treatment for 9 months with calcitriol or calcium in combination with alendronate significantly increases both vertebral and femoral neck density (from 3.8% to 4.5% and from 0.61% to 2.36% respectively) in osteopenic postmenopausal women. The effects of both combinations on bone mass are clearly greater than those achieved by calcium monotherapy.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
骨化三醇与阿仑膦酸钠联合治疗绝经期低骨量妇女。
血清骨化三醇水平随着年龄的增长而下降,这与饮食摄入减少或肠道对维生素d的吸收不良有关。这些水平的下降影响老年性骨质减少的发展,这可以通过服用阿仑膦酸钠和钙有效地预防。为了评估阿仑膦酸钠和骨化三醇联合治疗对骨密度(BMD)的影响,我们对152名55-75岁的绝经后骨质减少妇女进行了为期9个月的随访。他们被分成三组。第一组每隔一天给予0.25微克合成1,25-二羟基维生素D3加10毫克阿仑膦酸钠治疗。第二组给予相同剂量的阿仑膦酸钠加钙(500 mg/天)。第三组只服用钙(500毫克/天)。在腰椎和股骨颈水平处测量骨密度。在治疗初期和结束时进行相同的骨代谢生化分析。三组的生物学参数基线值差异无统计学意义。阿仑膦酸钠加钙治疗导致总碱性磷酸酶和羟基脯氨酸尿显著减少,腰椎和股骨骨密度显著增加。在阿仑膦酸钠加骨化三醇组观察到相同的变化,除了股骨骨密度没有明显改善。这些结果表明,骨化三醇或钙联合阿仑膦酸钠连续治疗9个月可显著增加绝经后骨质减少妇女的椎体和股骨颈密度(分别从3.8%增加到4.5%和从0.61%增加到2.36%)。这两种组合对骨量的影响明显大于钙单药治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Tyrosinase induction and inactivation in normal cultured human melanocytes by endothelin-1. Distribution of aquaporin-9 in the rat: an immunohistochemical study. Otsuka Long-Evans Tokushima fatty (OLETF) rat is not a suitable animal model for the study of angiopathic diabetic retinopathy. Atheroprotective properties of nifedipine. The effects of rofecoxib on 24-h ambulatory blood pressure and heart rate monitoring in patients with hypertension and osteoarthritis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1