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

医学 丙酸氟替卡松 哮喘 早晨 优势比 吸入器 氟替卡松 皮质类固醇 逻辑回归 肾上腺功能不全 内科学 糖皮质激素 队列 泼尼松龙 内分泌学
作者
Vincent Brennan,Julie Martin‐Grace,Garrett Greene,Karen Heverin,Christopher Mulvey,Tom McCartan,Lorna Lombard,Joanne Walsh,Elaine MacHale,Shari Srinivasan,Michael O’Reilly,Chris Thompson,Richard W. Costello,Mark Sherlock
出处
期刊:The Journal of Allergy and Clinical Immunology: In Practice [Elsevier]
卷期号:10 (10): 2614-2623 被引量:11
标识
DOI:10.1016/j.jaip.2022.05.031
摘要

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.
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