Balance between macrophage migration inhibitory factor and sCD74 predicts outcome in patients with acute decompensation of cirrhosis

Macrophage migration inhibitory factor (MIF) is an inflammatory cytokine and an important regulator of innate immune responses. We hypothesised that serum concentrations of MIF are associated with disease severity and outcome in patients with decompensated cirrhosis and acute-on-chronic liver failur...

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Veröffentlicht in:JHEP reports 2021-04, Vol.3 (2), p.100221-100221, Article 100221
Hauptverfasser: Wirtz, Theresa H., Reuken, Philipp A., Jansen, Christian, Fischer, Petra, Bergmann, Irina, Backhaus, Christina, Emontzpohl, Christoph, Reißing, Johanna, Brandt, Elisa F., Koenen, M. Teresa, Schneider, Kai M., Schierwagen, Robert, Brol, Maximilian J., Chang, Johannes, Zimmermann, Henning W., Köse-Vogel, Nilay, Eggermann, Thomas, Kurth, Ingo, Stoppe, Christian, Bucala, Richard, Bernhagen, Jürgen, Praktiknjo, Michael, Stallmach, Andreas, Trautwein, Christian, Trebicka, Jonel, Bruns, Tony, Berres, Marie-Luise
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Sprache:eng
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Zusammenfassung:Macrophage migration inhibitory factor (MIF) is an inflammatory cytokine and an important regulator of innate immune responses. We hypothesised that serum concentrations of MIF are associated with disease severity and outcome in patients with decompensated cirrhosis and acute-on-chronic liver failure (ACLF). Circulating concentrations of MIF and its soluble receptor CD74 (sCD74) were determined in sera from 292 patients with acute decompensation of cirrhosis defined as new onset or worsening of ascites requiring hospitalisation. Of those, 78 (27%) had ACLF. Short-term mortality was assessed 90 days after inclusion. Although serum concentrations of MIF and sCD74 did not correlate with liver function parameters or ACLF, higher MIF (optimum cut-off >2.3 ng/ml) and lower concentrations of sCD74 (optimum cut-off
ISSN:2589-5559
2589-5559
DOI:10.1016/j.jhepr.2020.100221