Insulin treatment improves the systemic inflammatory reaction to severe trauma

Jeschke, Marc G. and Klein, Dagmar and Herndon, David N. (2004) Insulin treatment improves the systemic inflammatory reaction to severe trauma. ANNALS OF SURGERY, 239 (4). pp. 553-560. ISSN 0003-4932,

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Abstract

Objective: Determine the effect of insulin on the systemic inflammatory response, pro- and anti-inflammatory cytokines and hepatic acute-phase-response in severely burned pediatric patients. Summary Background Data: The systemic inflammatory and hepatic acute-phase-response contribute to hypermetabolism, multi-organ failure, and mortality. Insulin has been recently shown to decrease mortality and to prevent the incidence of multi-organ failure in critically ill patients; however, the underlying mechanisms have not been defined. Methods: Thirteen thermally injured children received insulin to maintain blood glucose at a range from 120 to 180 mg/dl, 15 children received no insulin with blood glucose levels also at range from 120 to 180 mg/dl and served as controls. Our outcome measures encompassed the effect of insulin on pro-inflammatory mediators, the hepatic acute-phase-response, fat, and the IGF-I system. Results: Insulin administration decreased pro-inflammatory cytokines and proteins, while increasing constitutive-hepatic proteins (P < 0.05). Burned children receiving insulin required significantly less albumin substitution to maintain normal levels compared with control (P < 0.05). Insulin decreased free fatty acids and serum triglycerides when compared with controls (P < 0.05). Serum IGF-I and IGFBP-3 significantly increased with insulin administration (P < 0.05). Conclusion: Insulin attenuates the inflammatory response by decreasing the pro-inflammatory and increasing the anti-inflammatory cascade, thus restoring systemic homeostasis, which has been shown critical for organ function and survival in critically ill patients.

Item Type: Article
Uncontrolled Keywords: GROWTH-FACTOR-I; ACUTE-PHASE RESPONSE; CRITICALLY-ILL; TRIGLYCERIDE SECRETION; INCREASED MORTALITY; GENE-TRANSCRIPTION; PROTEIN-SYNTHESIS; HORMONE TREATMENT; CRITICAL ILLNESS; BURN PATIENTS;
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Chirurgie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 21 Jul 2021 12:23
Last Modified: 21 Jul 2021 12:23
URI: https://pred.uni-regensburg.de/id/eprint/37761

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