Abstract

BackgroundSepsis, a dysregulated host response following infection, is associated with massive immune activation and high mortality rates. There is still a need to define further risk factors and laboratory parameters predicting the clinical course. Iron metabolism is regulated by both, the body’s iron status and the immune response. Iron itself is required for erythropoiesis but also for many cellular and metabolic functions. Moreover, iron availability is a critical determinant in infections because it is an essential nutrient for most microbes but also impacts on immune function and intravascular oxidative stress. Herein, we used a prospective study design to investigate the putative impact of serum iron parameters on the outcome of sepsis.MethodsSerum markers of iron metabolism were measured in a prospective cohort of 61 patients (37 males, 24 females) with sepsis defined by Sepsis-3 criteria in a medical intensive care unit (ICU) and compared between survivors and non-survivors. Regulation of iron parameters in patients stratified by focus of infection and co-medication as well as association of the markers with sepsis severity scores and survival were investigated with linear and logistic regression corrected for sex and age effects.ResultsPositive correlations of increased serum iron and ferritin concentrations upon ICU admission with the severity of organ failure (SOFA score) and with mortality were observed. Moreover, high TF-Sat, elevated ferritin and serum iron levels and low transferrin concentrations were associated with reduced survival. A logistic regression model consisting of SOFA and transferrin saturation (SOFA–TF-Sat) had the best predictive power for survival in septic ICU patients. Of note, administration of blood transfusions prior to ICU admission resulted in increased TF-Sat and reduced survival of septic patients.ConclusionsOur study could show an important impact of serum iron parameters on the outcome of sepsis. Furthermore, we identified transferrin saturation as a stand-alone predictor of sepsis survival and as a parameter of iron metabolism which may in a combined model improve the prediction power of the SOFA score.Trial registrationThe study was carried out in accordance with the recommendations of the Declaration of Helsinki on biomedical research. The study was approved by the institutional ethics review board of the Medical University Innsbruck (study AN2013-0006).

Highlights

  • Sepsis, a dysregulated host response following infection, is associated with massive immune activation and high mortality rates

  • We aimed to investigate the efficacy of serum iron parameters for predicting sepsis mortality in a prospective cohort of sepsis patients treated in an intensive care unit (ICU)

  • This study aimed to investigate the efficacy of serum iron parameters for predicting sepsis mortality in a prospective cohort of sepsis patients treated in an ICU and identified transferrin saturation (TF-Sat) as additional laboratory parameter to increase the predictive power of the Sepsis-related organ failure assessment score (SOFA) score, yielding our SOFA - TF-Sat model

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Summary

Introduction

A dysregulated host response following infection, is associated with massive immune activation and high mortality rates. Iron metabolism is regulated by both, the body’s iron status and the immune response. Iron availability is a critical determinant in infections because it is an essential nutrient for most microbes and impacts on immune function and intravascular oxidative stress. Sepsis is a manifestation of infections that is characterized by life-threatening organ dysfunction considered to be caused by a dysregulated host response [1]. A balanced body iron homeostasis is essential for basic metabolic functions [1, 5]. Iron is transported within the circulation following binding to transferrin (Tf) and taken up by metabolically active cells via transferrin receptor (TfR1) [5]. Excess iron is stored within ferritin (Ft) to avoid toxicity of pro-oxidative labile iron (Additional file 1)

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