Cytokine production and hospital mortality in patients with sepsis-induced stress hyperglycemia

J Infect. 2007 Oct;55(4):340-6. doi: 10.1016/j.jinf.2007.05.177. Epub 2007 Jul 13.

Abstract

Objectives: To investigate whether stress hyperglycemia affects the production of the main pro- and anti-inflammatory cytokines and the 28-day hospital mortality in patients with severe sepsis.

Methods: The study included 62 patients with severe sepsis, divided in three groups according to their glycemic profile within 24h after admission: patients with stress hyperglycemia (group SH, n=16), diabetes mellitus type II (group DM, n=27), and normal glucose levels (group NG, n=19). The serum levels of the cytokines TNF-alpha, IL-6, IL-10 and TGFbeta-1 were measured within 24h after admission.

Results: A higher percentage of septic patients with stress hyperglycemia died compared to diabetic patients (43.7 vs. 14.8%) and group NG (43.7 vs. 5.2%). Group SH had higher SOFA score and levels of IL-6 and IL-10 than group DM and group NG. It also had higher levels of TNF-alpha than group DM but not group NG. There was no difference in the levels of TGFbeta-1 among the three groups. Non-survivors had higher levels of IL-10, no difference was detected for IL-6, TNF-alpha, IL-10/TNF-alpha ratio and TGFbeta-1. Interleukin-10 values, mean fasting glucose values and age were found as prognostic factors associated with outcome.

Conclusions: Stress hyperglycemia is associated with increased cytokine production and an adverse clinical outcome in patients with severe sepsis.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Cytokines / biosynthesis*
  • Cytokines / blood
  • Female
  • Hospital Mortality
  • Humans
  • Hyperglycemia / etiology
  • Hyperglycemia / immunology*
  • Hyperglycemia / mortality*
  • Interleukin-10 / biosynthesis
  • Interleukin-10 / blood
  • Interleukin-6 / biosynthesis
  • Interleukin-6 / blood
  • Male
  • Middle Aged
  • Sepsis / complications
  • Sepsis / immunology*
  • Transforming Growth Factor beta1 / biosynthesis
  • Transforming Growth Factor beta1 / blood
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Cytokines
  • Interleukin-6
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha
  • Interleukin-10