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哮喘患者使用口服和吸入糖皮质激素与骨质疏松症及脆性骨折风险:两项基于人群的巢式病例对照研究。

Risk of osteoporosis and fragility fractures in asthma due to oral and inhaled corticosteroids: two population-based nested case-control studies.

机构信息

School of Medicine, Division of Respiratory Medicine, University of Nottingham, Nottingham, UK

School of Medicine, Division of Respiratory Medicine, University of Nottingham, Nottingham, UK.

出版信息

Thorax. 2021 Jan;76(1):21-28. doi: 10.1136/thoraxjnl-2020-215664. Epub 2020 Oct 21.

Abstract

BACKGROUND

Inhaled (ICS) and oral (OCS) corticosteroids are used widely in asthma; however, the risk of osteoporosis and fragility fracture (FF) due to corticosteroids in asthma is not well-established.

METHODS

We conducted two nested case-control studies using linked data from the Clinical Practice Research Datalink (CPRD) and Hospital Episode Statistics (HES) databases. Using an asthma cohort, we separately identified patients with osteoporosis or FF and gender-, age- and practice-matched controls. Conditional logistic regression was used to determine the association between ICS and OCS exposure, and the risk of osteoporosis or FF. The prevalence of patients receiving at least one bisphosphonate was also calculated.

RESULTS

There was a dose-response relationship between both cumulative dose and number of OCS/ICS prescriptions within the previous year, and risk of osteoporosis or FF. After adjusting for confounders, people receiving more OCS prescriptions (≥9 vs 0) had a 4.50 (95% CI 3.21 to 6.11) and 2.16 (95% CI 1.56 to 3.32) increased risk of osteoporosis and FF, respectively. For ICS (≥11 vs 0) the ORs were 1.60 (95% CI 1.22 to 2.10) and 1.31 (95% CI 1.02 to 1.68). The cumulative dose had a similar impact, with those receiving more OCS or ICS being at greater risk. The prevalence of patients taking ≥9 OCS and at least one bisphosphonate prescription was just 50.6% and 48.4% for osteoporosis and FF, respectively.

CONCLUSIONS

The findings suggest that exposure to OCS or ICS is an independent risk factors for bone health in patients with asthma. Steroid administration at the lowest possible level to maintain asthma control is recommended.

摘要

背景

吸入性(ICS)和口服(OCS)皮质类固醇在哮喘中广泛应用;然而,哮喘患者因皮质类固醇导致骨质疏松症和脆性骨折(FF)的风险尚未得到充分证实。

方法

我们使用来自临床实践研究数据链(CPRD)和医院入院统计数据(HES)数据库的链接数据进行了两项嵌套病例对照研究。使用哮喘队列,我们分别确定了骨质疏松症或 FF 患者以及性别、年龄和实践匹配的对照患者。使用条件逻辑回归确定 ICS 和 OCS 暴露与骨质疏松症或 FF 风险之间的关联。还计算了至少接受一种双膦酸盐治疗的患者的患病率。

结果

在过去一年中,累积剂量和 OCS/ICS 处方数量均与骨质疏松症或 FF 的风险呈剂量反应关系。在校正混杂因素后,接受更多 OCS 处方(≥9 与 0)的患者发生骨质疏松症和 FF 的风险分别增加了 4.50(95%CI 3.21 至 6.11)和 2.16(95%CI 1.56 至 3.32)。对于 ICS(≥11 与 0),OR 分别为 1.60(95%CI 1.22 至 2.10)和 1.31(95%CI 1.02 至 1.68)。累积剂量也有类似的影响,接受更多 OCS 或 ICS 的患者风险更高。接受≥9 OCS 和至少一种双膦酸盐处方的患者分别只有 50.6%和 48.4%的骨质疏松症和 FF 患者。

结论

研究结果表明,OCS 或 ICS 暴露是哮喘患者骨健康的独立危险因素。建议以尽可能低的水平给予类固醇以维持哮喘控制。

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