Level of MFAP4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosis

Background & Aims: Prognostic models of cirrhosis underestimate disease severity for patients with cirrhosis and ascites. Microfibrillar-associated protein 4 (MFAP4) is an extracellular matrix protein linked to hepatic neoangiogenesis and fibrogenesis. We investigated ascites MFAP4 as a pred...

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Main Authors: Nikolaj Torp, Mads Israelsen, Bjørn Madsen, Philipp Lutz, Christian Jansen, Christian Strassburg, Christian Mortensen, Anne Wilkens Knudsen, Grith Lykke Sorensen, Uffe Holmskov, Anders Schlosser, Maja Thiele, Jonel Trebicka, Aleksander Krag
Format: Article
Language:English
Published: Elsevier 2021-06-01
Series:JHEP Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S258955592100063X
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collection DOAJ
language English
format Article
sources DOAJ
author Nikolaj Torp
Mads Israelsen
Bjørn Madsen
Philipp Lutz
Christian Jansen
Christian Strassburg
Christian Mortensen
Anne Wilkens Knudsen
Grith Lykke Sorensen
Uffe Holmskov
Anders Schlosser
Maja Thiele
Jonel Trebicka
Aleksander Krag
spellingShingle Nikolaj Torp
Mads Israelsen
Bjørn Madsen
Philipp Lutz
Christian Jansen
Christian Strassburg
Christian Mortensen
Anne Wilkens Knudsen
Grith Lykke Sorensen
Uffe Holmskov
Anders Schlosser
Maja Thiele
Jonel Trebicka
Aleksander Krag
Level of MFAP4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosis
JHEP Reports
Fibrosis
Decompensated
Mortality
Biomarker
Prognosis
Liver disease
author_facet Nikolaj Torp
Mads Israelsen
Bjørn Madsen
Philipp Lutz
Christian Jansen
Christian Strassburg
Christian Mortensen
Anne Wilkens Knudsen
Grith Lykke Sorensen
Uffe Holmskov
Anders Schlosser
Maja Thiele
Jonel Trebicka
Aleksander Krag
author_sort Nikolaj Torp
title Level of MFAP4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosis
title_short Level of MFAP4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosis
title_full Level of MFAP4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosis
title_fullStr Level of MFAP4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosis
title_full_unstemmed Level of MFAP4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosis
title_sort level of mfap4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosis
publisher Elsevier
series JHEP Reports
issn 2589-5559
publishDate 2021-06-01
description Background &amp; Aims: Prognostic models of cirrhosis underestimate disease severity for patients with cirrhosis and ascites. Microfibrillar-associated protein 4 (MFAP4) is an extracellular matrix protein linked to hepatic neoangiogenesis and fibrogenesis. We investigated ascites MFAP4 as a predictor of transplant-free survival in patients with cirrhosis and ascites. Methods: A dual-centre observational study of patients with cirrhosis and ascites recruited consecutively in relation to a paracentesis was carried out. Patients were followed up for 1 year, until death or liver transplantation (LTx). Ascites MFAP4 was tested with the model for end-stage liver disease (MELD-Na), CLIF Consortium Acute Decompensation (CLIF-C AD), and Child-Pugh score in Cox regression models. Results: Ninety-three patients requiring paracentesis were included. Median ascites MFAP4 was 29.7 U/L [22.3–41.3], and MELD-Na was 19 [16–23]. A low MELD-Na score (<20) was observed in 49 patients (53%). During follow-up, 20 patients died (22%), and 6 received LTx (6%). High ascites MFAP4 (>29.7 U/L) was associated with 1-year transplant-free survival (p = 0.002). In Cox regression, ascites MFAP4 and MELD-Na independently predicted 1-year transplant-free survival (hazard ratio [HR] = 0.97, p = 0.03, and HR = 1.08, p = 0.01, respectively). Ascites MFAP4 and CLIF-C AD also predicted survival independently (HR = 0.96, p = 0.02, and HR = 1.05, p = 0.03, respectively), whereas only ascites MFAP4 did, controlling for the Child-Pugh score (HR = 0.97, p = 0.03, and HR = 1.18, p = 0.16, respectively). For patients with MELD-Na <20, ascites MFAP4 but not ascites protein predicted 1-year transplant-free survival (HR 0.91, p = 0.02, and HR = 0.94, p = 0.17, respectively). Conclusions: Ascites MFAP4 predicts 1-year transplant-free survival in patients with cirrhosis and ascites. In patients with low MELD-Na scores, ascites MFAP4, but not total ascites protein, significantly predicted 1-year transplant-free survival. Lay summary: Patients with cirrhosis who have fluid in the abdomen, ascites, are at an increased risk of death and in need for liver transplantation. Our study identified patients with ascites and a poor prognosis by measuring microfibrillar associated protein 4 (MFAP4), a protein present in the abdominal fluid. Patients with low levels of the MFAP4 protein are at particularly increased risk of death or liver transplantation, suggesting that clinical care should be intensified in this group of patients.
topic Fibrosis
Decompensated
Mortality
Biomarker
Prognosis
Liver disease
url http://www.sciencedirect.com/science/article/pii/S258955592100063X
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spelling doaj-c51fc06253d54badb91ebd90031bee152021-06-05T06:10:33ZengElsevierJHEP Reports2589-55592021-06-0133100287Level of MFAP4 in ascites independently predicts 1-year transplant-free survival in patients with cirrhosisNikolaj Torp0Mads Israelsen1Bjørn Madsen2Philipp Lutz3Christian Jansen4Christian Strassburg5Christian Mortensen6Anne Wilkens Knudsen7Grith Lykke Sorensen8Uffe Holmskov9Anders Schlosser10Maja Thiele11Jonel Trebicka12Aleksander Krag13Department of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark; Institute of Clinical Research, University of Southern Denmark, Odense, DenmarkDepartment of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark; Institute of Clinical Research, University of Southern Denmark, Odense, DenmarkDepartment of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark; Institute of Clinical Research, University of Southern Denmark, Odense, DenmarkDepartment of Internal Medicine I, University of Bonn, Bonn, GermanyDepartment of Internal Medicine I, University of Bonn, Bonn, GermanyDepartment of Internal Medicine I, University of Bonn, Bonn, GermanyGastro Unit, Medical Division, Copenhagen University Hospital, Hvidovre, DenmarkGastro Unit, Medical Division, Copenhagen University Hospital, Hvidovre, DenmarkInstitute of Molecular Medicine, University of Southern Denmark, Odense, DenmarkInstitute of Molecular Medicine, University of Southern Denmark, Odense, DenmarkInstitute of Molecular Medicine, University of Southern Denmark, Odense, DenmarkDepartment of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark; Institute of Clinical Research, University of Southern Denmark, Odense, DenmarkInstitute of Clinical Research, University of Southern Denmark, Odense, Denmark; Department of Internal Medicine I, University Hospital of Frankfurt, Frankfurt, Germany; European Foundation for the Study of Chronic Liver Failure (EF-CLIF), Barcelona, Spain; Institute for Bioengineering of Catalonia, Barcelona, SpainDepartment of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark; Institute of Clinical Research, University of Southern Denmark, Odense, Denmark; Corresponding author. Address: Odense Liver Research Centre, Department of Gastroenterology and Hepatology, Odense University Hospital, Kloevervaenget 10, 5000 Odense C, Denmark.Background &amp; Aims: Prognostic models of cirrhosis underestimate disease severity for patients with cirrhosis and ascites. Microfibrillar-associated protein 4 (MFAP4) is an extracellular matrix protein linked to hepatic neoangiogenesis and fibrogenesis. We investigated ascites MFAP4 as a predictor of transplant-free survival in patients with cirrhosis and ascites. Methods: A dual-centre observational study of patients with cirrhosis and ascites recruited consecutively in relation to a paracentesis was carried out. Patients were followed up for 1 year, until death or liver transplantation (LTx). Ascites MFAP4 was tested with the model for end-stage liver disease (MELD-Na), CLIF Consortium Acute Decompensation (CLIF-C AD), and Child-Pugh score in Cox regression models. Results: Ninety-three patients requiring paracentesis were included. Median ascites MFAP4 was 29.7 U/L [22.3–41.3], and MELD-Na was 19 [16–23]. A low MELD-Na score (<20) was observed in 49 patients (53%). During follow-up, 20 patients died (22%), and 6 received LTx (6%). High ascites MFAP4 (>29.7 U/L) was associated with 1-year transplant-free survival (p = 0.002). In Cox regression, ascites MFAP4 and MELD-Na independently predicted 1-year transplant-free survival (hazard ratio [HR] = 0.97, p = 0.03, and HR = 1.08, p = 0.01, respectively). Ascites MFAP4 and CLIF-C AD also predicted survival independently (HR = 0.96, p = 0.02, and HR = 1.05, p = 0.03, respectively), whereas only ascites MFAP4 did, controlling for the Child-Pugh score (HR = 0.97, p = 0.03, and HR = 1.18, p = 0.16, respectively). For patients with MELD-Na <20, ascites MFAP4 but not ascites protein predicted 1-year transplant-free survival (HR 0.91, p = 0.02, and HR = 0.94, p = 0.17, respectively). Conclusions: Ascites MFAP4 predicts 1-year transplant-free survival in patients with cirrhosis and ascites. In patients with low MELD-Na scores, ascites MFAP4, but not total ascites protein, significantly predicted 1-year transplant-free survival. Lay summary: Patients with cirrhosis who have fluid in the abdomen, ascites, are at an increased risk of death and in need for liver transplantation. Our study identified patients with ascites and a poor prognosis by measuring microfibrillar associated protein 4 (MFAP4), a protein present in the abdominal fluid. Patients with low levels of the MFAP4 protein are at particularly increased risk of death or liver transplantation, suggesting that clinical care should be intensified in this group of patients.http://www.sciencedirect.com/science/article/pii/S258955592100063XFibrosisDecompensatedMortalityBiomarkerPrognosisLiver disease