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Serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis

Liver cirrhosis represents the common end-stage of chronic liver diseases regardless of its etiology. Patients with compensated disease are mostly asymptomatic, however, progression to a decompensated disease stage is common. The available stratification strategies are often unsuitable to identify p...

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Autores principales: Benz, Fabian, Bogen, Andreas, Praktiknjo, Michael, Jansen, Christian, Meyer, Carsten, Wree, Alexander, Demir, Muenevver, Loosen, Sven, Vucur, Mihael, Schierwagen, Robert, Tacke, Frank, Trebicka, Jonel, Roderburg, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164617/
https://www.ncbi.nlm.nih.gov/pubmed/32302330
http://dx.doi.org/10.1371/journal.pone.0231701
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author Benz, Fabian
Bogen, Andreas
Praktiknjo, Michael
Jansen, Christian
Meyer, Carsten
Wree, Alexander
Demir, Muenevver
Loosen, Sven
Vucur, Mihael
Schierwagen, Robert
Tacke, Frank
Trebicka, Jonel
Roderburg, Christoph
author_facet Benz, Fabian
Bogen, Andreas
Praktiknjo, Michael
Jansen, Christian
Meyer, Carsten
Wree, Alexander
Demir, Muenevver
Loosen, Sven
Vucur, Mihael
Schierwagen, Robert
Tacke, Frank
Trebicka, Jonel
Roderburg, Christoph
author_sort Benz, Fabian
collection PubMed
description Liver cirrhosis represents the common end-stage of chronic liver diseases regardless of its etiology. Patients with compensated disease are mostly asymptomatic, however, progression to a decompensated disease stage is common. The available stratification strategies are often unsuitable to identify patients with a higher risk for disease progression and a limited prognosis. SIBLINGs, soluble glycophosphoproteins, are secreted into the blood by immune-cells. While osteopontin, the most prominent member of the SIBLINGs family, has been repeatedly associated with liver cirrhosis, data on the diagnostic and/or prognostic value of bone sialoprotein (BSP) are scarce and partly inconclusive. In this study, we analyzed the diagnostic and prognostic potential of circulating BSP in comparison to other standard laboratory markers in a large cohort of patients with liver cirrhosis receiving transjugular intrahepatic portosystemic shunt (TIPS). Serum levels of BSP were similar in patients with different disease stages and were not indicative for prognosis. Interestingly, BSP serum levels did correlate inversely with portal pressure, as well as its surrogates such as platelet count, the portal vein cross-sectional area and correlated positively with the portal venous velocity. In summary, our data highlight that BSP might represent a previously unrecognized marker for portal hypertension in patients with liver cirrhosis.
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spelling pubmed-71646172020-04-22 Serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis Benz, Fabian Bogen, Andreas Praktiknjo, Michael Jansen, Christian Meyer, Carsten Wree, Alexander Demir, Muenevver Loosen, Sven Vucur, Mihael Schierwagen, Robert Tacke, Frank Trebicka, Jonel Roderburg, Christoph PLoS One Research Article Liver cirrhosis represents the common end-stage of chronic liver diseases regardless of its etiology. Patients with compensated disease are mostly asymptomatic, however, progression to a decompensated disease stage is common. The available stratification strategies are often unsuitable to identify patients with a higher risk for disease progression and a limited prognosis. SIBLINGs, soluble glycophosphoproteins, are secreted into the blood by immune-cells. While osteopontin, the most prominent member of the SIBLINGs family, has been repeatedly associated with liver cirrhosis, data on the diagnostic and/or prognostic value of bone sialoprotein (BSP) are scarce and partly inconclusive. In this study, we analyzed the diagnostic and prognostic potential of circulating BSP in comparison to other standard laboratory markers in a large cohort of patients with liver cirrhosis receiving transjugular intrahepatic portosystemic shunt (TIPS). Serum levels of BSP were similar in patients with different disease stages and were not indicative for prognosis. Interestingly, BSP serum levels did correlate inversely with portal pressure, as well as its surrogates such as platelet count, the portal vein cross-sectional area and correlated positively with the portal venous velocity. In summary, our data highlight that BSP might represent a previously unrecognized marker for portal hypertension in patients with liver cirrhosis. Public Library of Science 2020-04-17 /pmc/articles/PMC7164617/ /pubmed/32302330 http://dx.doi.org/10.1371/journal.pone.0231701 Text en © 2020 Benz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Benz, Fabian
Bogen, Andreas
Praktiknjo, Michael
Jansen, Christian
Meyer, Carsten
Wree, Alexander
Demir, Muenevver
Loosen, Sven
Vucur, Mihael
Schierwagen, Robert
Tacke, Frank
Trebicka, Jonel
Roderburg, Christoph
Serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis
title Serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis
title_full Serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis
title_fullStr Serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis
title_full_unstemmed Serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis
title_short Serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis
title_sort serum levels of bone sialoprotein correlate with portal pressure in patients with liver cirrhosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164617/
https://www.ncbi.nlm.nih.gov/pubmed/32302330
http://dx.doi.org/10.1371/journal.pone.0231701
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