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口服和吸入糖皮质激素对哮喘患者肾上腺功能不全的影响。

The Contribution of Oral and Inhaled Glucocorticoids to Adrenal Insufficiency in Asthma.

机构信息

Department of Medicine, Royal College of Surgeons in Ireland Beaumont Campus, Dublin, Ireland.

Department of Clinical Biochemistry, Beaumont Hospital, Dublin, Ireland.

出版信息

J Allergy Clin Immunol Pract. 2022 Oct;10(10):2614-2623. doi: 10.1016/j.jaip.2022.05.031. Epub 2022 Jun 10.

Abstract

BACKGROUND

Exposure to any form of glucocorticoid preparation is associated with a risk of adrenal insufficiency (AI).

OBJECTIVE

To establish the contribution of oral corticosteroid (OCS) and inhaled corticosteroid (ICS) exposure to the risk of AI in a cohort of patients (n = 80) with severe, uncontrolled asthma.

METHODS

We compiled individualized cumulative OCS and ICS exposure data using a combination of health care records and electronic inhaler monitoring using an Inhaler Compliance Assessment device and estimated the risk of AI for each participant using a morning serum cortisol concentration.

RESULTS

The predicted prevalence of AI based on morning cortisol concentrations was 25% (20 of 80). Participants on maintenance OCS therapy had the highest risk of AI at 60% (6 of 10) compared with 17% (11 of 65) in those with no recent OCS exposure. Morning serum cortisol correlated negatively with both OCS exposure (mg/kg prednisolone) (r = -0.4; P < .0002) and ICS exposure (mg/kg fluticasone propionate) (r = -0.26; P = .019). Logistic regression of risk of AI against the number of standard treatment courses of OCS demonstrated a positive relationship although this did not reach statistical significance (odds ratio, 1.41; 95% CI, 0.97-2.05; P = .073). Logistic regression analysis, categorizing patients as high-risk AI (cortisol <130 nmol/L) or not (cortisol >130 nmol/L), showed that cumulative ICS exposure remained a significant predictor of AI, even when exposure to OCS was controlled for (odds ratio, 2.17 per 1 mg/kg increase in cumulative fluticasone propionate exposure; 95% CI, 1.06-4.42; P = .033).

CONCLUSIONS

Our data suggest that AI is common among patients with asthma and highlights that the risk of AI is associated with both high-dose ICS therapy and intermittent treatment courses of OCS.

摘要

背景

接触任何形式的糖皮质激素制剂都与肾上腺皮质功能不全(AI)的风险相关。

目的

在一组患有严重、控制不佳的哮喘的患者(n=80)中,确定口服皮质类固醇(OCS)和吸入皮质类固醇(ICS)暴露对 AI 风险的贡献。

方法

我们使用健康记录和电子吸入器监测(使用吸入器依从性评估装置)相结合,编制了个体化累积 OCS 和 ICS 暴露数据,并使用早晨血清皮质醇浓度来估计每位参与者发生 AI 的风险。

结果

基于早晨皮质醇浓度预测的 AI 患病率为 25%(80 例中的 20 例)。与没有最近 OCS 暴露的患者(17%,65 例中的 11 例)相比,接受维持性 OCS 治疗的患者 AI 风险最高,为 60%(10 例中的 6 例)。早晨血清皮质醇与 OCS 暴露(mg/kg 泼尼松龙)(r=-0.4;P<.0002)和 ICS 暴露(mg/kg 丙酸氟替卡松)(r=-0.26;P=.019)呈负相关。对 AI 风险与 OCS 标准治疗疗程数的对数回归显示出正相关,尽管这没有达到统计学意义(比值比,1.41;95%CI,0.97-2.05;P=0.073)。将患者分类为高风险 AI(皮质醇<130nmol/L)或非高风险 AI(皮质醇>130nmol/L)的逻辑回归分析显示,即使控制了 OCS 暴露,累积 ICS 暴露仍然是 AI 的一个显著预测因子(比值比,每增加 1mg/kg 累积丙酸氟替卡松暴露增加 2.17;95%CI,1.06-4.42;P=0.033)。

结论

我们的数据表明,AI 在哮喘患者中很常见,并强调 AI 的风险与高剂量 ICS 治疗和 OCS 的间歇性治疗疗程都有关。

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