Serum cytokines and critical illness-related corticosteroid insufficiency

Yong Soo Kwon1, Gee Young Suh, Kyeongman Jeon

  • 1Department of Internal Medicine, Chonnam National University Hospital, Gwangju, Republic of Korea.

Insights

Elevated cytokines like IL-6, IL-10, and TNF-α are linked to a specific type of critical illness-related corticosteroid insufficiency (CIRCI) with low cortisol response. This finding helps understand CIRCI subgroups better.

Area of Science:

  • Critical care medicine
  • Endocrinology
  • Immunology

Background:

  • Critical illness-related corticosteroid insufficiency (CIRCI) is common in ICUs.
  • Specific cytokine associations with CIRCI subgroups are not well understood.
  • Adrenal function assessment is crucial for managing critically ill patients.

Purpose of the Study:

  • To investigate the association between specific serum cytokine levels and subgroups of patients with CIRCI.
  • To differentiate cytokine profiles in patients with normal adrenal function, low basal cortisol, and low cortisol response.

Main Methods:

  • Retrospective analysis of data from a prospective ICU study on adrenal function.
  • Diagnosis of CIRCI based on basal and stimulated cortisol levels.
  • Categorization of CIRCI patients into low basal cortisol (LBC) and low Δ cortisol (LDC) groups.
  • Comparison of serum cytokine levels (IL-6, IL-10, TNF-α) among normal (NOM), LBC, and LDC groups.

Main Results:

  • Overall CIRCI incidence was 43.9% among 82 analyzed patients.
  • The LDC group (55.6% of CIRCI patients) showed significantly higher IL-6 and IL-10 levels than NOM and LBC groups (p < 0.01).
  • The LDC group also had significantly higher TNF-α compared to the LBC group (p = 0.002).
  • No significant cytokine differences were found between NOM and LBC groups.

Conclusions:

  • Elevated cytokines, particularly IL-6, IL-10, and TNF-α, are associated with adrenal dysfunction in a specific subset of CIRCI patients.
  • The low Δ cortisol subgroup (LDC) exhibits a distinct inflammatory profile compared to those with normal adrenal function or low basal cortisol.
  • These findings contribute to a better understanding of the heterogeneity of CIRCI and its inflammatory underpinnings.
Abstract

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