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接受长期吸入性类固醇治疗哮喘患者的骨矿物质密度与骨折风险

Bone mineral density and the risk of fracture in patients receiving long-term inhaled steroid therapy for asthma.

作者信息

Toogood J H, Baskerville J C, Markov A E, Hodsman A B, Fraher L J, Jennings B, Haddad R G, Drost D

机构信息

Department of Medicine, Victoria Hospital, London, Ontario, Canada.

出版信息

J Allergy Clin Immunol. 1995 Aug;96(2):157-66. doi: 10.1016/s0091-6749(95)70003-x.

Abstract

To determine whether high-dose or prolonged inhaled steroid therapy for asthma increases a patient's risk of osteoporosis and fracture, we measured bone density in 26 men and 43 women (41 postmenopausal, all of whom had received supplemental estrogen therapy) after treatment with an inhaled steroid for 10.1 +/- 5.5 years and oral prednisone for 10.7 +/- 9.7 years (mean +/- SD). Most had stopped receiving prednisone since commencing the inhaled steroid therapy. We found that bone densities (adjusted for age and sex to yield a z score) were lower in association with higher daily doses of inhaled steroid (p = 0.013 ANCOVA) and with the duration of past prednisone therapy (p = 0.032). Larger cumulative inhaled steroid doses were associated with higher bone densities (p = 0.002) and a reduction in the numbers of patients at risk of fracture. Bone density also increased with the amount of supplemental estrogen therapy (p = 0.058) and, at equivalent levels of inhaled and oral steroid use, women showed higher bone density z scores than did men. Women with a lifetime dose of inhaled steroid greater than 3 gm had normal bone density regardless of the amount of past or current prednisone use or the current dose of inhaled steroid. These data indicate that the daily dose, but not the duration, of inhaled steroid therapy may adversely affect bone density, and that estrogen therapy may offset this bone-depleting effect in postmenopausal women.

摘要

为了确定高剂量或长期吸入性类固醇治疗哮喘是否会增加患者患骨质疏松症和骨折的风险,我们对26名男性和43名女性(41名绝经后女性,她们均接受了雌激素补充治疗)进行了骨密度测量。这些患者接受吸入性类固醇治疗10.1±5.5年,口服泼尼松治疗10.7±9.7年(均值±标准差)。自开始吸入性类固醇治疗后,大多数患者已停止服用泼尼松。我们发现,经年龄和性别校正以得出z值后,骨密度与较高的每日吸入性类固醇剂量相关(协方差分析,p = 0.013),也与过去泼尼松治疗的持续时间相关(p = 0.032)。更大的吸入性类固醇累积剂量与更高的骨密度相关(p = 0.002),且骨折风险患者数量减少。骨密度也随着雌激素补充治疗量的增加而升高(p = 0.058),并且在吸入性和口服类固醇使用量相当的情况下,女性的骨密度z值高于男性。吸入性类固醇终生剂量大于3克的女性,无论过去或目前泼尼松的使用量或目前吸入性类固醇的剂量如何,其骨密度均正常。这些数据表明,吸入性类固醇治疗的每日剂量而非治疗持续时间可能会对骨密度产生不利影响,并且雌激素治疗可能会抵消绝经后女性的这种骨质流失效应。

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