金天格胶囊在预防绝经后女性骨质疏松性骨折中的作用

目的观察金天格胶囊在治疗绝经后女性骨质疏松的疗效,判断其预防骨折发生的概率。方法选取绝经后骨质疏松女性238名,随机分为4组,第1组:金天格59例,第2组:钙尔奇D+金天格58例,第3组:钙尔奇D+金天格+阿仑膦酸钠63例,第4组:钙尔奇D+阿仑膦酸钠58例;服药剂量:金天格1.2mg,tid;钙尔奇D 600mg qd;福善美70mg qw。分别在服药前、服药后3、6个月检测骨密度(bone mineral densities,BMD)、血清1型原胶原N-端前肽(PINP)和1型胶原交联C-末端肽(CTX)。结果各组骨密度无明显变化(P〉0.05);服药3个月,4组的PINP分别下降了18....

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Published in中国骨质疏松杂志 Vol. 21; no. 12; pp. 1498 - 1500
Main Author 甘强 谭祖建 周明全 胡维
Format Journal Article
LanguageChinese
Published 重庆市中山医院骨科中心,重庆,400013 2015
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ISSN1006-7108
DOI10.3969/j.issn.1006-7108.2015.12.018

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Summary:目的观察金天格胶囊在治疗绝经后女性骨质疏松的疗效,判断其预防骨折发生的概率。方法选取绝经后骨质疏松女性238名,随机分为4组,第1组:金天格59例,第2组:钙尔奇D+金天格58例,第3组:钙尔奇D+金天格+阿仑膦酸钠63例,第4组:钙尔奇D+阿仑膦酸钠58例;服药剂量:金天格1.2mg,tid;钙尔奇D 600mg qd;福善美70mg qw。分别在服药前、服药后3、6个月检测骨密度(bone mineral densities,BMD)、血清1型原胶原N-端前肽(PINP)和1型胶原交联C-末端肽(CTX)。结果各组骨密度无明显变化(P〉0.05);服药3个月,4组的PINP分别下降了18.2%、22.3%、62.3%、55.8%,CTX分别下降了24.3%、29.7%、68.7%、57.8%;服药6个月,4组的PINP分别下降了19.4%、23.6%、63.5%、62%,CTX分别下降了28.1%、28.3%、69.9%、64.5%。结论金天格胶囊可以明显降低骨转化指标,能有效辅助治疗骨质疏松和预防骨折的发生。
Bibliography:Osteoporosis; Jintiange capsule; Bone turnover markers; Bone mineral density
Objective To observetheefficacy of Jintiangecapsuleon thetreatment of osteoporosis and to judgetheprobability of osteoporotic fractureprevention in postmenopausal women. Methods Two hundred and thirty-eight postmenopausal women with osteoporosis wereselected and randomly divided into 4 groups,Group one( Jintiangecapsulegroup,n = 59),Group two( calcium and Jintiangecapsulegroup,n = 58),Group three( calcium and Jintiangecapsuleand bisphosphonategroup,n = 63),and Group four( calcium and bisphosphonategroup,n = 58). Thedosageof thedrugs was 1. 2mg of Jintiangecapsule,tid,600 mg of calcium,qd,and 70 mg of bisphosphonates,qw. Bonemineral densities( BMD),serum procollagen typeI amino-terminal propeptide( PINP),and serum C-terminal cross-linked telopeptides of typeI collagen( CTX) weredetected beforeand after 3months and 6 months of thetreatment,respectively. Results BMD was not obviously changed in each group( P〉0. 05). After 3months of trea
ISSN:1006-7108
DOI:10.3969/j.issn.1006-7108.2015.12.018