Mebrahtu Teumzghi F, Morgan Ann W, Keeley Adam, Baxter Paul D, Stewart Paul M, Pujades-Rodriguez Mar
Leeds Institute of Biomedical and Clinical Sciences, School of Medicine, University of Leeds, Leeds, United Kingdom.
Leeds Institute of Cardiovascular and Metabolic Medicine, School of Medicine, University of Leeds, Leeds, United Kingdom.
J Clin Endocrinol Metab. 2019 Sep 1;104(9):3757-3767. doi: 10.1210/jc.2019-00153.
Adrenal insufficiency and Cushing syndrome are known adverse events of glucocorticoids. However, no population estimates of dose-related risks are available.
To investigate dose-related risks of adrenal dysfunction and death in adults with six chronic inflammatory diseases treated with oral glucocorticoids.
Retrospective, record-linkage, open-cohort study spanning primary and hospital care in England.
A total of 70,638 oral glucocorticoid users and 41,166 nonusers aged ≥18 years registered in 389 practices in 1998 to 2017.
Incidence rates and hazard ratios (HRs) of diagnosed adrenal dysfunction and death.
During a median follow-up of 5.5 years, 183 patients had glucocorticoid-induced adrenal insufficiency and 248 had glucocorticoid-induced Cushing syndrome. A total of 22,317 (31.6%) and 7544 (18.3%) deaths occurred among glucocorticoid users and nonusers, respectively. The incidence of all outcomes increased with higher current daily and cumulative doses. For adrenal insufficiency, the increases in HRs were 1.07 (95% CI: 1.04 to 1.09) for every increase of 5 mg per day and 2.25 (95% CI: 2.15 to 2.35) per 1000 mg of cumulative prednisolone-equivalent dose over the past year. The respective increases in HRs for Cushing syndrome were 1.09 (95% CI: 1.08 to 1.11) and 2.31 (95% CI: 2.23 to 2.40) and for mortality 1.26 (95% CI: 2.24 to 1.28) and 2.05 (95% CI: 2.04 to 2.06).
We report a high glucocorticoid dose-dependent increased risk of adrenal adverse events and death. The low observed absolute risk of adrenal insufficiency highlights a potential lack of awareness and a need for increased physician and patient education about the risks of adrenal dysfunction induced by glucocorticoids.
肾上腺功能不全和库欣综合征是已知的糖皮质激素不良事件。然而,尚无与剂量相关风险的人群估计数据。
调查接受口服糖皮质激素治疗的患有六种慢性炎症性疾病的成年人中肾上腺功能障碍和死亡的剂量相关风险。
一项回顾性、记录链接、开放队列研究,涵盖英格兰的初级和医院护理。
1998年至2017年在389家医疗机构登记的70638名年龄≥18岁的口服糖皮质激素使用者和41166名非使用者。
诊断为肾上腺功能障碍和死亡的发病率及风险比(HRs)。
在中位随访5.5年期间,183例患者发生糖皮质激素诱导的肾上腺功能不全,248例患者发生糖皮质激素诱导的库欣综合征。糖皮质激素使用者和非使用者分别有22317例(31.6%)和7544例(18.3%)死亡。所有结局的发病率均随当前每日剂量和累积剂量的增加而升高。对于肾上腺功能不全,每日每增加5毫克,HRs升高1.07(95%CI:1.04至1.09),过去一年每1000毫克累积泼尼松等效剂量,HRs升高2.25(95%CI:2.15至2.35)。库欣综合征的HRs相应升高分别为1.09(95%CI:1.08至1.11)和2.31(95%CI:2.23至2.40),死亡率的HRs升高分别为1.26(95%CI:2.24至1.28)和2.05(95%CI:2.04至2.06)。
我们报告了糖皮质激素剂量依赖性增加的肾上腺不良事件和死亡风险。观察到的肾上腺功能不全的绝对风险较低,这突出表明可能缺乏认识,且需要加强医生和患者对糖皮质激素诱导的肾上腺功能障碍风险的教育。