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应用阿仑膦酸钠预防免疫性疾病糖皮质激素性骨质疏松症 被引量:3

Alendronate prevents steroid-induced osteoporosis in patients with rheumatic diseases
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摘要 目的观察阿仑膦酸钠预防糖皮质激素性骨质疏松症的骨密度以及骨代谢指标的变化。方法选择140例患有风湿性疾病需长期应用糖皮质激素的非骨质疏松病人,包括系统性红斑狼疮、多发性肌炎、皮肌炎、干燥综合征等。将上述病人随机分为:阿仑膦酸钠组74例(阿仑膦酸钠10mg,1次/d,加上钙尔奇D0.6g,1次/d),单纯钙剂组66例(钙尔奇0.6g,1次/d),疗程24周。分别测定用药前,用药24周后的骨密度、血钙、血磷、血清碱性磷酸酶(AKP)、血清骨钙素(BGP)、尿I型胶原交联氨基末端肽(NTX)的水平。结果阿仑膦酸钠治疗组骨密度较治疗前有不同程度的增加,其中腰椎、股骨颈、大转子、WARD′S区的骨密度分别增加6.1%,6.3%,3.3%,2.2%,BGP较治疗前上升,但差异无统计学意义,尿NTX较治疗前下降(P〈0.05),而对照组的腰椎骨密度下降了8.7%,股骨颈下降9.1%(P〈0.01),大转子下降7.7%、WARD′S区下降6.4%(P〈0.05),血钙、磷、BGP、尿NTX变化差异无统计学意义。结论阿仑膦酸钠可以提高骨密度,具有预防糖皮质激素性骨质疏松的作用;单用钙剂并不能阻止激素诱导的骨质疏松的发生。 Objective To investigate the effects of alendronate (Alen) on the prevention of systemic glucocorticoid-induced osteoporosis in patients with rheumatic diseases. Methods 140 patients suffering from rheumatic diseases, including systemic lupus erythematosus, polymyositis, dermatomyositis, and Sjogren′s syndrome, with normal bone mineral density (BMD) and treated with oral glucocorticoids were randomly divided into 2 groups : Alen + calcium group ( n = 74 ) receiving Alen 10 mg once a day and caltrate D 600 0. 6 g once a day for 24 weeks and control group ( n = 66) receiving caltrate D 600 0. 6 g once a day for 24 weeks. The BMD and biomarkers of bone turnover were measured at baseline and 24 weeks after initiating glucocorticoid therapy. Results After 24 weeks, the BMD values at lumbar spine, femoral neck, major trochanter, and Ward′ s triangle increased by 6. 1%, 6. 3% , 3.3% , and 2.2% respectively compared with those at baseline (all P 〈0.05) , however, those of the control group decreased by 8. 7% , 9. 1% , 7.7% , and 6. 4% respectively ( P 〈 0.01, P 〈 0.05 ) , and the BMD levels at lumbar spine and femoral neck 24 weeks later of the Alen + calcium group were both higher than those of the control group (P 〈0.01,P 〈0.05). 24 weeks later the level of urine cross linked N-telopeptides of type Ⅰ collagen (NTX) of the Alen + calcium group decreased ( P 〈 0. 05 ), and the blood osteocalcin (BGP) of the Alen + calcium group increased, however, not significantly ( P 〉 0. 05 ). There were no significant differences in serum AKP and BGP and urine NTX 24 weeks later between these 2 groups. Conclusion Improving BMD, alendronate plays an important role in the prevention of glucocorticoid-induced osteoporosis. However, calcium treatment alone fails to prevent the loss of bone.
出处 《中华医学杂志》 CAS CSCD 北大核心 2008年第27期1888-1891,共4页 National Medical Journal of China
关键词 阿仑膦酸钠 骨密度 糖皮质激素 骨质疏松症 Alendronate Bone mineral density Glucocorticoid Osteoporosis
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参考文献12

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同被引文献35

  • 1陈小晖,祝宇鹏,杨胜宏,程祥荣,程勇,张俊.套筒冠义齿用于牙周病修复治疗后的根周骨质变化[J].口腔医学研究,2004,20(5):532-534. 被引量:11
  • 2马绪臣,王松灵,王虎等.口腔颌面医学影像诊断学[M].北京:人民卫生出版社,2004.151.
  • 3American College of Rheumatology Ad Hoc Committee on Glucocorticoid-Induced Osteoporosis.Recommendations for the prevention and treatment of glucocorticoid-induced osteoporosis:2001update.Arthritis Rheum,2001,44:1496-1503.
  • 4廖二元.骨质疏松症.见:陆再英,钟南山,主编.内科学.第7版.北京:人民卫生出版社,2008,835-840.
  • 5季秉琦.口腔粘膜学.第2版.北京:人民卫生出版社,2005,61-62.
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  • 7Bone HG,Hosking D,Devogelaer JP,et al.Ten years' experience with alendronate for osteoporosis in postmenopaussl women.N Engl J Med,2004,350:1189-1199.
  • 8de Groen PC,Lubbe DF,Hirsch LJ,et al.Esophagitis associated with the use of alendronate.N Engl J Med,1996,335:1016-1021.
  • 9Donahue JG,Chant KA,Andrade SE,et al.Gastric and duodenal safety of daily alendronate.Arch Intern Med,2002,162:936-942.
  • 10G6mez V,Xiao SY.Alendronate-induced esophagitis in an elderly woman.Int J Clin Exp Pathol,2009,2:200-203.

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