<sup>1</sup>H NMR Based Metabolomics in Human Sepsis and Healthy Serum

Early diagnosis is essential but challenging in severe sepsis. Quantifying and comparing metabolite concentrations in serum has been suggested as a new diagnostic tool. Here we used proton nuclear magnetic resonance spectroscopy (<sup>1</sup>H NMR) based metabolomics to analyze the possi...

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Main Authors: Henna Jaurila, Vesa Koivukangas, Marjo Koskela, Fiia Gäddnäs, Sami Myllymaa, Arja Kullaa, Tuula Salo, Tero I. Ala-Kokko
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:Metabolites
Subjects:
nmr
agp
Online Access:https://www.mdpi.com/2218-1989/10/2/70
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spelling doaj-9e307ba4dc534fd9ad4eb379a94f89402020-11-25T01:42:27ZengMDPI AGMetabolites2218-19892020-02-011027010.3390/metabo10020070metabo10020070<sup>1</sup>H NMR Based Metabolomics in Human Sepsis and Healthy SerumHenna Jaurila0Vesa Koivukangas1Marjo Koskela2Fiia Gäddnäs3Sami Myllymaa4Arja Kullaa5Tuula Salo6Tero I. Ala-Kokko7Research Group of Surgery, Anesthesia and Intensive Care, Oulu University Hospital, PO. Box 21, 90029 Oulu, FinlandResearch Group of Surgery, Anesthesia and Intensive Care, Oulu University Hospital, PO. Box 21, 90029 Oulu, FinlandResearch Group of Surgery, Anesthesia and Intensive Care, Oulu University Hospital, PO. Box 21, 90029 Oulu, FinlandResearch Group of Surgery, Anesthesia and Intensive Care, Oulu University Hospital, PO. Box 21, 90029 Oulu, FinlandDepartment of Applied Physics &amp; SIB Labs, University of Eastern Finland, P.O. Box 1627, 70211 Kuopio, FinlandInstitute of Dentistry, Faculty of Health Sciences, University of Eastern Finland, P.O. Box 1627, 70211 Kuopio, FinlandMedical Research Center Oulu, University of Oulu, P.O. Box 5281, 90014 Oulu, FinlandResearch Group of Surgery, Anesthesia and Intensive Care, Oulu University Hospital, PO. Box 21, 90029 Oulu, FinlandEarly diagnosis is essential but challenging in severe sepsis. Quantifying and comparing metabolite concentrations in serum has been suggested as a new diagnostic tool. Here we used proton nuclear magnetic resonance spectroscopy (<sup>1</sup>H NMR) based metabolomics to analyze the possible differences in metabolite concentrations between sera taken from septic patients and healthy controls, as well as between sera of surviving and non-surviving sepsis patients. We took serum samples from 44 sepsis patients when the first sepsis induced organ dysfunction was found. Serum samples were also collected from 14 age and gender matched healthy controls. The samples were analyzed by quantitative <sup>1</sup>H NMR spectroscopy for non-lipid metabolites. We found that the serum levels of glucose, glycine, 3-hydroxybutyrate, creatinine and glycoprotein acetyls (mostly alpha-1-acid glycoprotein, AGP) were significantly (<i>p</i> &lt; 0.05) higher in sepsis compared to healthy sera, whereas citrate and histidine were significantly (<i>p</i> &lt; 0.05) lower in sepsis patients compared to healthy controls. We found statistically significantly higher serum lactate and citrate concentrations in non-survivors compared to 30-day survivors. According to our study, 3-hydroxybutyrate, citrate, glycine, histidine, and AGP are candidates for further studies to enable identification of phenotype association in the early stages of sepsis.https://www.mdpi.com/2218-1989/10/2/70sepsishuman serumnmrmetabolomics3-hydroxybutyratecitrateglycinehistidineagp
collection DOAJ
language English
format Article
sources DOAJ
author Henna Jaurila
Vesa Koivukangas
Marjo Koskela
Fiia Gäddnäs
Sami Myllymaa
Arja Kullaa
Tuula Salo
Tero I. Ala-Kokko
spellingShingle Henna Jaurila
Vesa Koivukangas
Marjo Koskela
Fiia Gäddnäs
Sami Myllymaa
Arja Kullaa
Tuula Salo
Tero I. Ala-Kokko
<sup>1</sup>H NMR Based Metabolomics in Human Sepsis and Healthy Serum
Metabolites
sepsis
human serum
nmr
metabolomics
3-hydroxybutyrate
citrate
glycine
histidine
agp
author_facet Henna Jaurila
Vesa Koivukangas
Marjo Koskela
Fiia Gäddnäs
Sami Myllymaa
Arja Kullaa
Tuula Salo
Tero I. Ala-Kokko
author_sort Henna Jaurila
title <sup>1</sup>H NMR Based Metabolomics in Human Sepsis and Healthy Serum
title_short <sup>1</sup>H NMR Based Metabolomics in Human Sepsis and Healthy Serum
title_full <sup>1</sup>H NMR Based Metabolomics in Human Sepsis and Healthy Serum
title_fullStr <sup>1</sup>H NMR Based Metabolomics in Human Sepsis and Healthy Serum
title_full_unstemmed <sup>1</sup>H NMR Based Metabolomics in Human Sepsis and Healthy Serum
title_sort <sup>1</sup>h nmr based metabolomics in human sepsis and healthy serum
publisher MDPI AG
series Metabolites
issn 2218-1989
publishDate 2020-02-01
description Early diagnosis is essential but challenging in severe sepsis. Quantifying and comparing metabolite concentrations in serum has been suggested as a new diagnostic tool. Here we used proton nuclear magnetic resonance spectroscopy (<sup>1</sup>H NMR) based metabolomics to analyze the possible differences in metabolite concentrations between sera taken from septic patients and healthy controls, as well as between sera of surviving and non-surviving sepsis patients. We took serum samples from 44 sepsis patients when the first sepsis induced organ dysfunction was found. Serum samples were also collected from 14 age and gender matched healthy controls. The samples were analyzed by quantitative <sup>1</sup>H NMR spectroscopy for non-lipid metabolites. We found that the serum levels of glucose, glycine, 3-hydroxybutyrate, creatinine and glycoprotein acetyls (mostly alpha-1-acid glycoprotein, AGP) were significantly (<i>p</i> &lt; 0.05) higher in sepsis compared to healthy sera, whereas citrate and histidine were significantly (<i>p</i> &lt; 0.05) lower in sepsis patients compared to healthy controls. We found statistically significantly higher serum lactate and citrate concentrations in non-survivors compared to 30-day survivors. According to our study, 3-hydroxybutyrate, citrate, glycine, histidine, and AGP are candidates for further studies to enable identification of phenotype association in the early stages of sepsis.
topic sepsis
human serum
nmr
metabolomics
3-hydroxybutyrate
citrate
glycine
histidine
agp
url https://www.mdpi.com/2218-1989/10/2/70
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