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Corticotropin-stimulated steroid profiles to predict shock development and mortality in sepsis: From the HYPRESS study

医学 败血症 安慰剂 氢化可的松 糖皮质激素 休克(循环) 感染性休克 内科学 皮质酮 肾上腺功能不全 内分泌学 刺激 激素 病理 替代医学
作者
Josef Briegel,Patrick Möhnle,Didier Keh,Johanna M. Lindner,Anna C. Vetter,Holger Bogatsch,Dorothea Lange,Sandra Frank,Ludwig Christian Hinske,Djillali Annane,Michael Vogeser,Michael Bauer,Thorsten Brenner,Patrick Meybohm,Markus A. Weigand,Matthias Gründling,Markus Löffler,Michael Kiehntopf,Frank Bloos,Gunnar Elke
出处
期刊:Critical Care [BioMed Central]
卷期号:26 (1) 被引量:9
标识
DOI:10.1186/s13054-022-04224-5
摘要

Abstract Rationale Steroid profiles in combination with a corticotropin stimulation test provide information about steroidogenesis and its functional reserves in critically ill patients. Objectives We investigated whether steroid profiles before and after corticotropin stimulation can predict the risk of in-hospital death in sepsis. Methods An exploratory data analysis of a double blind, randomized trial in sepsis (HYPRESS [HYdrocortisone for PRevention of Septic Shock]) was performed. The trial included adult patients with sepsis who were not in shock and were randomly assigned to placebo or hydrocortisone treatment. Corticotropin tests were performed in patients prior to randomization and in healthy subjects. Cortisol and precursors of glucocorticoids (17-OH-progesterone, 11-desoxycortisol) and mineralocorticoids (11-desoxycorticosterone, corticosterone) were analyzed using the multi-analyte stable isotope dilution method (LC–MS/MS). Measurement results from healthy subjects were used to determine reference ranges, and those from placebo patients to predict in-hospital mortality. Measurements and main results Corticotropin tests from 180 patients and 20 volunteers were included. Compared to healthy subjects, patients with sepsis had elevated levels of 11-desoxycorticosterone and 11-desoxycortisol, consistent with activation of both glucocorticoid and mineralocorticoid pathways. After stimulation with corticotropin, the cortisol response was subnormal in 12% and the corticosterone response in 50% of sepsis patients. In placebo patients ( n = 90), a corticotropin-stimulated cortisol-to-corticosterone ratio > 32.2 predicted in-hospital mortality (AUC 0.8 CI 0.70–0.88; sensitivity 83%; and specificity 78%). This ratio also predicted risk of shock development and 90-day mortality. Conclusions In this exploratory analysis, we found that in sepsis mineralocorticoid steroidogenesis was more frequently impaired than glucocorticoid steroidogenesis. The corticotropin-stimulated cortisol-to-corticosterone ratio predicts the risk of in-hospital death. Trial registration Clinical trial registered with www.clinicaltrials.gov Identifier: NCT00670254. Registered 1 May 2008, https://clinicaltrials.gov/ct2/show/NCT00670254 .
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