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骨化三醇治疗在防治骨质流失和骨折中的疗效:定性评价。

The efficacy of calcitriol therapy in the management of bone loss and fractures: a qualitative review.

机构信息

Department of Radiation Oncology, University of Rochester, Rochester, NY, USA.

出版信息

Osteoporos Int. 2010 Jul;21(7):1133-49. doi: 10.1007/s00198-009-1136-2. Epub 2009 Dec 4.

Abstract

UNLABELLED

Osteoporosis, a skeletal disorder characterized by a reduction in bone strength, increases fracture risk. Primary osteoporosis is usually a result of reduced bone mineral density as a consequence of natural aging. Secondary osteoporosis is usually a result of a disease, such as cystic fibrosis, or medical treatment, such as corticosteroids or cancer treatment.

INTRODUCTION

Currently, ten million Americans are osteoporotic and an additional 34 million have the precursor condition, osteopenia. Osteoporosis leads to 1.5 million fractures and 500,000 hospitalizations annually. Osteoporosis-related fractures increase mortality and reduce quality of life. Calcitriol, the active form of vitamin D, regulates intestinal calcium absorption, among other actions. During the past four decades, many clinical trials investigating the effect of calcitriol on bone loss have been performed.

METHODS

We conducted a systematic qualitative review of clinical trials that assessed calcitriol for the treatment of osteoporosis and bone loss. In these clinical trials, calcitriol was used as a monotherapy and in combination with other therapeutic bone agents.

RESULTS AND CONCLUSION

Studies using calcitriol monotherapy, although not conclusive, found that calcitriol slowed the rate of bone loss in a variety of populations. Calcitriol in combination with other therapeutic bone agents was shown to have additional bone-preserving effects when compared to the use of therapeutic bone agents alone. A common side-effect of calcitriol therapy was hypercalcemia and hypercalciuria, but the degree of hypercalcemia was mild. Recent research found that intermittent dosing can reduce hypercalcemia rates. Calcitriol, alone or in combination with other agents, should be considered for the therapy of osteoporosis.

摘要

目的

骨质疏松症是一种以骨强度降低为特征的骨骼疾病,会增加骨折风险。原发性骨质疏松症通常是由于自然衰老导致骨密度降低所致。继发性骨质疏松症通常是由于疾病(如囊性纤维化)或医学治疗(如皮质类固醇或癌症治疗)引起的。

简介

目前,有 1000 万美国人患有骨质疏松症,另有 3400 万人患有骨质疏松前期疾病——骨量减少症。骨质疏松症每年导致 150 万例骨折和 50 万例住院治疗。骨质疏松症相关骨折会增加死亡率并降低生活质量。骨化三醇是维生素 D 的活性形式,除了其他作用外,还可以调节肠道钙吸收。在过去的四十年中,已经进行了许多临床试验,以研究骨化三醇对骨丢失的影响。

方法

我们对评估骨化三醇治疗骨质疏松症和骨丢失的临床试验进行了系统的定性综述。在这些临床试验中,骨化三醇作为单一疗法和与其他治疗性骨制剂联合使用。

结果和结论

虽然使用骨化三醇单一疗法的研究尚无定论,但发现骨化三醇可减缓各种人群的骨丢失速度。与单独使用治疗性骨制剂相比,骨化三醇与其他治疗性骨制剂联合使用具有额外的骨保护作用。骨化三醇治疗的常见副作用是高钙血症和高钙尿症,但高钙血症的程度较轻。最近的研究发现,间歇性给药可以降低高钙血症的发生率。骨化三醇单独或与其他药物联合使用,应考虑用于骨质疏松症的治疗。

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