Suppr超能文献

继发性骨质疏松症:潜在疾病与糖皮质激素诱导的骨质疏松症风险

Secondary osteoporosis: underlying disease and the risk for glucocorticoid-induced osteoporosis.

作者信息

Boling Eugene P

机构信息

Department of Medicine, Loma Linda University, Rancho Cucamonga, California, USA.

出版信息

Clin Ther. 2004 Jan;26(1):1-14. doi: 10.1016/s0149-2918(04)90001-x.

Abstract

BACKGROUND

Chronic diseases of many organ systems require long-term (>or=1 year) treatment with glucocorticoids. Owing to the catabolic activity of glucocorticoid therapy, osteoporosis is a potential complication.

OBJECTIVES

This review discusses glucocorticoid-induced bone loss and the factors, including underlying disease, that increase the risk for osteoporosis. Therapeutic options for the prevention and treatment of glucocorticoid-induced osteoporosis (GIO) also are reviewed.

METHODS

A review of the English-language literature was conducted using the MEDLINE database and proceedings from scientific meetings. Search terms including glucocorticoid-induced osteoporosis, bone loss, and fracture were used to refine the search, and preference was given to studies published after 1990.

RESULTS

Long-term glucocorticoid treatment causes bone loss that is most precipitous in the first 6 months. Patients treated with glucocorticoids have additional risk factors for bone loss and osteoporosis that are associated with their primary disease. Chronic diseases can cause changes in bone metabolism, leading to bone loss in addition to that induced by glucocorticoids alone. Bone loss can be minimized through proper nutrition, weight-bearing exercise, calcium and vitamin D supplementation, and, where indicated, bisphosphonate treatment. The American College of Rheumatology Ad Hoc Committee on Glucocorticoid-Induced Osteoporosis guidelines recommend bisphosphonates for minimizing bone loss and fracture risk in patients at risk for GIO. Risedronate is indicated for the prevention and treatment of GIO, and alendronate is indicated for its treatment. Both risedronate and alendronate increase bone mineral density in patients at risk for GIO. Risedronate significantly reduces the incidence of vertebral fractures after 1 year of treatment (P<0.05). The effectiveness and tolerability of the bisphosphonates have not been established in pregnant women or pediatric patients.

CONCLUSIONS

Men and women initiating long-term glucocorticoid treatment and those with GIO should be concomitantly treated with effective osteoporosis therapy to reduce fracture risk and counseled on preventive lifestyle changes.

摘要

背景

许多器官系统的慢性疾病需要长期(≥1年)使用糖皮质激素治疗。由于糖皮质激素治疗具有分解代谢活性,骨质疏松症是一种潜在的并发症。

目的

本综述讨论糖皮质激素诱导的骨质流失以及增加骨质疏松症风险的因素,包括基础疾病。还综述了预防和治疗糖皮质激素诱导的骨质疏松症(GIO)的治疗选择。

方法

使用MEDLINE数据库和科学会议记录对英文文献进行综述。使用包括糖皮质激素诱导的骨质疏松症、骨质流失和骨折等检索词来细化搜索,并优先选择1990年后发表的研究。

结果

长期糖皮质激素治疗会导致骨质流失,在前6个月最为急剧。接受糖皮质激素治疗的患者有与原发性疾病相关的额外骨质流失和骨质疏松症风险因素。慢性疾病可导致骨代谢变化,除了单独由糖皮质激素引起的骨质流失外,还会导致骨质流失。通过适当的营养、负重锻炼、补充钙和维生素D,以及在必要时进行双膦酸盐治疗,可以将骨质流失降至最低。美国风湿病学会糖皮质激素诱导的骨质疏松症特设委员会指南建议使用双膦酸盐来降低GIO风险患者的骨质流失和骨折风险。利塞膦酸钠适用于预防和治疗GIO,阿仑膦酸钠适用于其治疗。利塞膦酸钠和阿仑膦酸钠均可增加GIO风险患者的骨密度。利塞膦酸钠在治疗1年后显著降低椎体骨折的发生率(P<0.05)。双膦酸盐在孕妇或儿科患者中的有效性和耐受性尚未确立。

结论

开始长期糖皮质激素治疗的男性和女性以及患有GIO的患者应同时接受有效的骨质疏松症治疗以降低骨折风险,并接受预防性生活方式改变的咨询。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验