Department of Medicine, Royal College of Surgeons in Ireland Beaumont Campus, Dublin, Ireland.
Department of Clinical Biochemistry, Beaumont Hospital, Dublin, Ireland.
J Allergy Clin Immunol Pract. 2022 Oct;10(10):2614-2623. doi: 10.1016/j.jaip.2022.05.031. Epub 2022 Jun 10.
Exposure to any form of glucocorticoid preparation is associated with a risk of adrenal insufficiency (AI).
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.
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.
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).
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.
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。
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。
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。
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)。
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。