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Increased plasma vaspin concentration in patients with sepsis: an exploratory examination

INTRODUCTION: Vaspin (visceral adipose tissue-derived serpin) was first described as an insulin-sensitizing adipose tissue hormone. Recently its anti-inflammatory function has been demonstrated. Since no appropriate data is available yet, we sought to investigate the plasma concentrations of vaspin...

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Autores principales: Motal, Michael C., Klaus, Daniel A., Lebherz-Eichinger, Diana, Tudor, Bianca, Hamp, Thomas, Wiegele, Marion, Seemann, Rudolf, Krenn, Claus G., Roth, Georg A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Society of Medical Biochemistry and Laboratory Medicine 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401312/
https://www.ncbi.nlm.nih.gov/pubmed/25672472
http://dx.doi.org/10.11613/BM.2015.011
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author Motal, Michael C.
Klaus, Daniel A.
Lebherz-Eichinger, Diana
Tudor, Bianca
Hamp, Thomas
Wiegele, Marion
Seemann, Rudolf
Krenn, Claus G.
Roth, Georg A.
author_facet Motal, Michael C.
Klaus, Daniel A.
Lebherz-Eichinger, Diana
Tudor, Bianca
Hamp, Thomas
Wiegele, Marion
Seemann, Rudolf
Krenn, Claus G.
Roth, Georg A.
author_sort Motal, Michael C.
collection PubMed
description INTRODUCTION: Vaspin (visceral adipose tissue-derived serpin) was first described as an insulin-sensitizing adipose tissue hormone. Recently its anti-inflammatory function has been demonstrated. Since no appropriate data is available yet, we sought to investigate the plasma concentrations of vaspin in sepsis. MATERIALS AND METHODS: 57 patients in intensive care, fulfilling the ACCP/SCCM criteria for sepsis, were prospectively included in our exploratory study. The control group consisted of 48 critically ill patients, receiving intensive care after trauma or major surgery. Patients were matched by age, sex, weight and existence of diabetes before statistical analysis. Blood samples were collected on the day of diagnosis. Vaspin plasma concentrations were measured using a commercially available enzyme-linked immunosorbent assay. RESULTS: Vaspin concentrations were significantly higher in septic patients compared to the control group (0.3 (0.1-0.4) ng/mL vs. 0.1 (0.0-0.3) ng/mL, respectively; P < 0.001). Vaspin concentration showed weak positive correlation with concentration of C-reactive protein (CRP) (r = 0.31, P = 0.002) as well as with SAPS II (r = 0.34, P = 0.002) and maximum of SOFA (r = 0.39, P < 0.001) scoring systems, as tested for the overall study population. CONCLUSION: In the sepsis group, vaspin plasma concentration was about three-fold as high as in the median surgical control group. We demonstrated a weak positive correlation between vaspin and CRP concentration, as well as with two scoring systems commonly used in intensive care settings. Although there seems to be some connection between vaspin and inflammation, its role in human sepsis needs to be evaluated further.
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spelling pubmed-44013122015-04-24 Increased plasma vaspin concentration in patients with sepsis: an exploratory examination Motal, Michael C. Klaus, Daniel A. Lebherz-Eichinger, Diana Tudor, Bianca Hamp, Thomas Wiegele, Marion Seemann, Rudolf Krenn, Claus G. Roth, Georg A. Biochem Med (Zagreb) Research Article INTRODUCTION: Vaspin (visceral adipose tissue-derived serpin) was first described as an insulin-sensitizing adipose tissue hormone. Recently its anti-inflammatory function has been demonstrated. Since no appropriate data is available yet, we sought to investigate the plasma concentrations of vaspin in sepsis. MATERIALS AND METHODS: 57 patients in intensive care, fulfilling the ACCP/SCCM criteria for sepsis, were prospectively included in our exploratory study. The control group consisted of 48 critically ill patients, receiving intensive care after trauma or major surgery. Patients were matched by age, sex, weight and existence of diabetes before statistical analysis. Blood samples were collected on the day of diagnosis. Vaspin plasma concentrations were measured using a commercially available enzyme-linked immunosorbent assay. RESULTS: Vaspin concentrations were significantly higher in septic patients compared to the control group (0.3 (0.1-0.4) ng/mL vs. 0.1 (0.0-0.3) ng/mL, respectively; P < 0.001). Vaspin concentration showed weak positive correlation with concentration of C-reactive protein (CRP) (r = 0.31, P = 0.002) as well as with SAPS II (r = 0.34, P = 0.002) and maximum of SOFA (r = 0.39, P < 0.001) scoring systems, as tested for the overall study population. CONCLUSION: In the sepsis group, vaspin plasma concentration was about three-fold as high as in the median surgical control group. We demonstrated a weak positive correlation between vaspin and CRP concentration, as well as with two scoring systems commonly used in intensive care settings. Although there seems to be some connection between vaspin and inflammation, its role in human sepsis needs to be evaluated further. Croatian Society of Medical Biochemistry and Laboratory Medicine 2015-02-15 /pmc/articles/PMC4401312/ /pubmed/25672472 http://dx.doi.org/10.11613/BM.2015.011 Text en
spellingShingle Research Article
Motal, Michael C.
Klaus, Daniel A.
Lebherz-Eichinger, Diana
Tudor, Bianca
Hamp, Thomas
Wiegele, Marion
Seemann, Rudolf
Krenn, Claus G.
Roth, Georg A.
Increased plasma vaspin concentration in patients with sepsis: an exploratory examination
title Increased plasma vaspin concentration in patients with sepsis: an exploratory examination
title_full Increased plasma vaspin concentration in patients with sepsis: an exploratory examination
title_fullStr Increased plasma vaspin concentration in patients with sepsis: an exploratory examination
title_full_unstemmed Increased plasma vaspin concentration in patients with sepsis: an exploratory examination
title_short Increased plasma vaspin concentration in patients with sepsis: an exploratory examination
title_sort increased plasma vaspin concentration in patients with sepsis: an exploratory examination
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401312/
https://www.ncbi.nlm.nih.gov/pubmed/25672472
http://dx.doi.org/10.11613/BM.2015.011
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