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Abstract
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.
Sprache
Englisch
Identifikatoren
ISSN: 1478-3223
eISSN: 1478-3231
DOI: 10.1111/liv.13133
Titel-ID: cdi_crossref_primary_10_1111_liv_13133
Format
–
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