Abstract

IntroductionSepsis is an important cause of mortality and morbidityfor preterm and hospitalized newborn babies. Today, nosingle test satisfies the criteria as being the ideal markerfor the early diagnosis of neonatal sepsis. Analysis of theentire metabolome is a promising method for determin-ing metabolic variations correlated with sepsis [1-6].Metabolomics profiling and sepsisWorks on metabolomics concerning sepsis conductedon animals and humans of different ages (newborn andadults) have recently been published and are presentedin Table 1. In septic patients compared to controls (inplasma and urine) it is possible to observe an increaseof metabolites which are part of the oxidative metabo-lism of fatty acids (such as hydroxybutyrate, acylcarni-tines and acetoacetate). Briefly stated, alterations in theglucose metabolism in critical conditions can be seen asa redistribution of glucose consumption from the mito-chondrial oxidative phosphorylation to other metabolicpathways, such as the production of lactate and the pen-tose phosphate pathway. In the study by Fanos et al. [7]a combined approach based on both nuclear magneticresonance (1)H-NMR) and gas-chromatography-mass

Highlights

  • Sepsis is an important cause of mortality and morbidity for preterm and hospitalized newborn babies

  • In septic patients compared to controls it is possible to observe an increase of metabolites which are part of the oxidative metabolism of fatty acids

  • Alterations in the glucose metabolism in critical conditions can be seen as a redistribution of glucose consumption from the mitochondrial oxidative phosphorylation to other metabolic pathways, such as the production of lactate and the pentose phosphate pathway

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Summary

Introduction

Sepsis is an important cause of mortality and morbidity for preterm and hospitalized newborn babies. Analysis of the entire metabolome is a promising method for determining metabolic variations correlated with sepsis [1,2,3,4,5,6]. In septic patients compared to controls (in plasma and urine) it is possible to observe an increase of metabolites which are part of the oxidative metabolism of fatty acids (such as hydroxybutyrate, acylcarnitines and acetoacetate). In the study by Fanos et al [7] a combined approach based on both nuclear magnetic resonance (1)H-NMR) and gas-chromatography-mass

Metabolite alterations
Acylcarnitines and glycerophosphatidylcholines
Conclusions
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