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骨化三醇对肾性骨病的早期治疗:一项前瞻性双盲研究。

Early therapy of renal bone disease with calcitriol: a prospective double-blind study.

作者信息

Baker L R, Abrams S M, Roe C J, Faugere M C, Fanti P, Subayti Y, Malluche H H

机构信息

Department of Nephrology, St. Bartholomew's Hospital, London, United Kingdom.

出版信息

Kidney Int Suppl. 1989 Nov;27:S140-2.

PMID:2699994
Abstract

The value of calcitriol administration in the management and prevention of renal bone disease was studied in a prospective double-blind manner in 16 patients with chronic renal impairment (creatinine clearance 20 to 59 ml per min). They were given either calcitriol at a dose of 0.25 to 0.5 micrograms daily (eight patients), or placebo. Transiliac crest bone biopsies were performed before entrance into the study and after 12 months of experimental observation. None of the patients were symptomatic or had biochemical or radiological evidence of bone disease. Of the thirteen patients who completed the study, initial serum 1,25(OH)2D levels were low in seven patients and parathyroid hormone levels were elevated in seven patients. Bone histology was abnormal in all patients. Calcitriol treatment was associated with a significant fall in serum phosphorus concentrations and alkaline phosphatase levels as well as with histological evidence of an amelioration of hyperparathyroid changes. In contrast to previous reports, no deterioration of renal function attributable to the treatment occurred, perhaps because a modest dose of calcitriol was employed combined with meticulous monitoring. Further investigation is required to determine whether alternative therapeutic strategies (smaller doses or intermittent therapy) may avoid the potential for suppressing bone turnover to abnormally low levels in the long term.

摘要

以前瞻性双盲方式对16例慢性肾功能损害患者(肌酐清除率为每分钟20至59毫升)进行了研究,以探讨骨化三醇在肾性骨病管理和预防中的价值。他们被给予每日剂量为0.25至0.5微克的骨化三醇(8例患者)或安慰剂。在进入研究前及实验观察12个月后进行了髂嵴骨活检。所有患者均无症状,也没有骨病的生化或放射学证据。在完成研究的13例患者中,7例患者初始血清1,25(OH)₂D水平较低,7例患者甲状旁腺激素水平升高。所有患者的骨组织学均异常。骨化三醇治疗与血清磷浓度和碱性磷酸酶水平显著下降以及甲状旁腺功能亢进改变改善的组织学证据相关。与先前的报告不同,未出现因治疗导致的肾功能恶化,这可能是因为使用了适度剂量的骨化三醇并进行了细致监测。需要进一步研究以确定替代治疗策略(较小剂量或间歇治疗)是否可避免长期将骨转换抑制到异常低水平的可能性。

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引用本文的文献

1
Calcitriol Suppression of Parathyroid Hormone Fails to Improve Skeletal Properties in an Animal Model of Chronic Kidney Disease.在慢性肾脏病动物模型中,骨化三醇抑制甲状旁腺激素未能改善骨骼特性。
Am J Nephrol. 2016;43(1):20-31. doi: 10.1159/000444423. Epub 2016 Feb 17.
2
Adynamic bone disease-bone and beyond.动力缺失性骨病——骨骼及其他方面
NDT Plus. 2008 Jun;1(3):135-47. doi: 10.1093/ndtplus/sfn040.
3
Renale osteodystrophie.肾性骨营养不良
Wien Med Wochenschr. 2013 Sep;163(17-18):403-8. doi: 10.1007/s10354-013-0195-3. Epub 2013 May 9.
4
Minimizing bone abnormalities in children with renal failure.将肾衰竭患儿的骨骼异常降至最低。
Paediatr Drugs. 2006;8(4):205-22. doi: 10.2165/00148581-200608040-00001.
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Vitamin D3 analogs and salmon calcitonin partially reverse the development of renal osteodystrophy in rats.维生素D3类似物和鲑鱼降钙素可部分逆转大鼠肾性骨营养不良的发展。
Calcif Tissue Int. 1995 Nov;57(5):385-91. doi: 10.1007/BF00302075.