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与全身和局部使用皮质类固醇相关的骨折风险。

Fracture risk associated with systemic and topical corticosteroids.

作者信息

Vestergaard P, Rejnmark L, Mosekilde L

机构信息

Department of Endocrinology and Metabolism C, Aarhus University Hospital, Aarhus, Denmark.

出版信息

J Intern Med. 2005 Apr;257(4):374-84. doi: 10.1111/j.1365-2796.2005.01467.x.

Abstract

OBJECTIVES

To study the fracture risk associated with the use of corticosteroids in any formulation and administration.

DESIGN

Case-control study.

SETTING

Community-based study in Denmark. Subjects. Cases were all subjects with any fracture sustained during the year 2000 (n = 124,655). For each case, three controls (n = 373,962) matched on age and gender were randomly drawn from the background population. Adjustments were made for concurrent diseases (lung diseases, rheumatic disorders), use of other drugs (inhaled bronchodilators), contacts to hospitals and general practitioners, and social variables.

RESULTS

An increased risk of any fracture, hip, spine, and forearm fractures was present with use of more than 2.5 mg of prednisolone or equivalent orally per day. For inhaled corticosteroids a limited increase in the risk of any fracture was present in users of more than 7.5 mg prednisolone equivalents per day (equivalent to 1875 mug of budesonide per day). However, no increase in the risk of hip, spine or forearm fractures was present in users of inhaled corticosteroids. For other topical corticosteroids (dermal, rectal, nasal, local application in the mouth, the eyes or the ears) no increase in fracture risk could be demonstrated even at high doses after adjustment for confounders.

CONCLUSIONS

Ingestion of more than 2.5 mg of oral prednisolone equivalents per day is associated with an increase in fracture risk. No increase is associated with inhaled corticosteroids except at daily dosages above 7.5 mg of prednisolone equivalents. No increase in fracture risk is associated with other forms of topical corticosteroids.

摘要

目的

研究使用任何剂型和给药方式的皮质类固醇与骨折风险之间的关联。

设计

病例对照研究。

地点

丹麦的社区研究。研究对象。病例为2000年期间发生任何骨折的所有受试者(n = 124,655)。对于每个病例,从背景人群中随机抽取三名年龄和性别匹配的对照(n = 373,962)。对并发疾病(肺部疾病、风湿性疾病)、其他药物的使用(吸入性支气管扩张剂)、与医院和全科医生的接触以及社会变量进行了调整。

结果

每天口服超过2.5毫克泼尼松龙或等效药物会增加任何骨折、髋部、脊柱和前臂骨折的风险。对于吸入性皮质类固醇,每天使用超过7.5毫克泼尼松龙等效物(相当于每天1875微克布地奈德)的使用者发生任何骨折的风险略有增加。然而,吸入性皮质类固醇使用者的髋部、脊柱或前臂骨折风险并未增加。对于其他局部用皮质类固醇(皮肤、直肠、鼻腔、口腔、眼睛或耳朵局部应用),即使在调整混杂因素后高剂量使用也未显示骨折风险增加。

结论

每天摄入超过2.5毫克口服泼尼松龙等效物与骨折风险增加相关。除了每天剂量超过7.5毫克泼尼松龙等效物外,吸入性皮质类固醇与骨折风险增加无关。其他形式的局部用皮质类固醇与骨折风险增加无关。

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