The ultra-acute steroid response to traumatic injury: a cohort study

Eur J Endocrinol. 2023 Mar 2;188(3):lvad024. doi: 10.1093/ejendo/lvad024.

Abstract

Objective: Trauma-induced steroid changes have been studied post-hospital admission, resulting in a lack of understanding of the speed and extent of the immediate endocrine response to injury. The Golden Hour study was designed to capture the ultra-acute response to traumatic injury.

Design: We conducted an observational cohort study including adult male trauma patients <60 years, with blood samples drawn ≤1 h of major trauma by pre-hospital emergency responders.

Methods: We recruited 31 adult male trauma patients (mean age 28 [range 19-59] years) with a mean injury severity score (ISS) of 16 (IQR 10-21). The median time to first sample was 35 (range 14-56) min, with follow-up samples collected 4-12 and 48-72 h post-injury. Serum steroids in patients and age- and sex-matched healthy controls (HCs) (n = 34) were analysed by tandem mass spectrometry.

Results: Within 1 h of injury, we observed an increase in glucocorticoid and adrenal androgen biosynthesis. Cortisol and 11-hydroxyandrostendione increased rapidly, whilst cortisone and 11-ketoandrostenedione decreased, reflective of increased cortisol and 11-oxygenated androgen precursor biosynthesis by 11β-hydroxylase and increased cortisol activation by 11β-hydroxysteroid dehydrogenase type 1. Active classic gonadal androgens testosterone and 5α-dihydrotestosterone decreased, whilst the active 11-oxygenated androgen 11-ketotestosterone maintained pre-injury levels.

Conclusions: Changes in steroid biosynthesis and metabolism occur within minutes of traumatic injury. Studies that address whether ultra-early changes in steroid metabolism are associated with patient outcomes are now required.

Keywords: 11-oxygenated androgens; glucocorticoids; major trauma; mass spectrometry; steroids.

Publication types

  • Observational Study

MeSH terms

  • Adult
  • Androgens* / metabolism
  • Cohort Studies
  • Dihydrotestosterone
  • Humans
  • Hydrocortisone*
  • Male
  • Middle Aged
  • Steroids / therapeutic use
  • Young Adult

Substances

  • Androgens
  • Hydrocortisone
  • Steroids
  • Dihydrotestosterone