4.7 Article

Mapping the Steroid Response to Major Trauma From Injury to Recovery: A Prospective Cohort Study

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 105, Issue 3, Pages 925-937

Publisher

ENDOCRINE SOC
DOI: 10.1210/clinem/dgz302

Keywords

major trauma; systemic inflammatory response syndrome; stress response; steroids; DHEA; testosterone

Funding

  1. Surgeon General's Casualty Nutrition Study (SGCNS), a Ministry of Defence
  2. University Hospitals Birmingham NHS Foundation Trust
  3. University of Birmingham
  4. National Institute for Health Research (NIHR) Surgical Reconstruction and Microbiology Research Centre (SRMRC)
  5. Drummond Trust Foundation
  6. NIHR Birmingham Biomedical Research Centre [BRC-1215-20009]
  7. MRC [MR/P021220/1] Funding Source: UKRI

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Context: Survival rates after severe injury are improving, but complication rates and outcomes are variable. Objective: This cohort study addressed the lack of longitudinal data on the steroid response to major trauma and during recovery. Design: We undertook a prospective, observational cohort study from time of injury to 6 months postinjury at a major UK trauma centre and a military rehabilitation unit, studying patients within 24 hours of major trauma (estimated New Injury Severity Score (NISS) > 15). Main outcome measures: We measured adrenal and gonadal steroids in serum and 24-hour urine by mass spectrometry, assessed muscle loss by ultrasound and nitrogen excretion, and recorded clinical outcomes (ventilator days, length of hospital stay, opioid use, incidence of organ dysfunction, and sepsis); results were analyzed by generalized mixed-effect linear models. Findings: We screened 996 multiple injured adults, approached 106, and recruited 95 eligible patients; 87 survived. We analyzed all male survivors <50 years not treated with steroids (N = 60; median age 27 [interquartile range 24-31] years; median NISS 34 [29-44]). Urinary nitrogen excretion and muscle loss peaked after 1 and 6 weeks, respectively. Serum testosterone, dehydroepiandrosterone, and dehydroepiandrosterone sulfate decreased immediately after trauma and took 2, 4, and more than 6 months, respectively, to recover; opioid treatment delayed dehydroepiandrosterone recovery in a dose-dependent fashion. Androgens and precursors correlated with SOFA score and probability of sepsis. Conclusion: The catabolic response to severe injury was accompanied by acute and sustained androgen suppression. Whether androgen supplementation improves health outcomes after major trauma requires further investigation.

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