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Macrophage activation marker, soluble CD 163, is an independent predictor of short‐term mortality in patients with cirrhosis and bacterial infection
Author(s) -
Tornai Tamas,
Vitalis Zsuzsanna,
Sipeki Nora,
Dinya Tamas,
Tornai David,
AntalSzalmas Peter,
Karanyi Zsolt,
Tornai Istvan,
Papp Maria
Publication year - 2016
Publication title -
liver international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.873
H-Index - 110
eISSN - 1478-3231
pISSN - 1478-3223
DOI - 10.1111/liv.13133
Subject(s) - medicine , hazard ratio , cirrhosis , gastroenterology , immunology , proportional hazards model , decompensation , confidence interval , disease , cd163 , macrophage , biology , biochemistry , in vitro
Background & Aims Innate immune system dysfunction is common in advanced cirrhosis, with a central role of the monocyte/macrophage system. Monocytes and macrophages express the scavenger receptor CD 163, which is regulated by inflammatory mediators. Cleavage of the receptor leads to the formation of soluble (s) CD 163 that represents an anti‐inflammatory response. We aimed to study the clinical importance of sCD 163 in cirrhosis. Methods Sera of 378 patients were assayed for sCD 163 by ELISA [193 outpatients and 185 patients with acute decompensation ( AD )]. A 5‐year follow‐up observational study was conducted to assess the possible association between sCD 163 level and poor disease outcomes. Results sCD 163 level was associated with disease severity, but not with the presence of varices or prior variceal bleeding. In outpatients, sCD 163 level did not predict the development of disease‐specific complications or the long‐term mortality. In patients with AD episode, sCD 163 level was significantly higher compared to outpatients but only in the presence of bacterial infection ( INF ) ( AD ‐ INF :4586, AD ‐ NON ‐ INF :3792 and outpatients: 3538 ng/ml, P < 0.015 and P = 0.001, respectively). sCD 163 level gradually increased according to severity of infection. During bacterial infections, high sCD 163 level (>7000 ng/ml) was associated with increased mortality rate (42% vs. 17%, P < 0.001) and was identified as an independent predictor of 28‐day mortality (hazard ratio:2.96, 95% confidence intervals:1.27–6.95) in multivariate Cox‐regression model comprising aetiology, co‐morbidity, model for end‐stage liver disease score and leucocyte count as covariates. Conclusions High sCD 163 level is useful to identify patients with high‐risk of death during an AD episode complicated by bacterial infection. This finding serves as an additional hint towards the significance of anti‐inflammatory response during bacterial infection.