2017, Number 5
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Ann Hepatol 2017; 16 (5)
Circulating levels of pentraxin-3 (PTX3) in patients with liver cirrhosis
Pereira JG, Erotides ST, Bansho ETO, Morato EF, Pinheiro JT, Muraro-Wildner L, Bazzo ML, Dantas-Corrêa EB, Schiavon LL, Narciso-Schiavon JL
Language: English
References: 36
Page: 780-787
PDF size: 163.11 Kb.
ABSTRACT
Background: Despite the circulating levels of PTX3 were related to the severity of various diseases, there are no studies investigating
its role in patients with liver cirrhosis. We aimed to study PTX3 levels in patients with liver cirrhosis.
Material and methods.
A prospective cohort study included 130 patients hospitalized for acute decompensation of liver cirrhosis, 29 stable cirrhotic
outpatients and 32 healthy controls evaluated in a tertiary hospital in Southern Brasil.
Results. The median PTX3 level was significantly
higher in stable cirrhotic patients compared to controls (2.6
vs. 1.1 ng/mL; p ‹ 0.001), hospitalized cirrhotic patients compared
to controls (3.8
vs. 1.1 ng/mL; p ‹ 0.001), and hospitalized cirrhotic patients compared to stable cirrhotic patients (3.8
vs. 2.6 ng/
mL; p = 0.001). A positive correlation was found between PTX3 and serum creatinine (r = 0.220; p = 0.012), Chronic Liver Failure -
Sequential Organ Failure Assessment score (CLIF-SOFA) (r = 0.220; p = 0.010), MELD (r = 0.279; p = 0.001) and Child-Pugh
score (r = 0.224; p = 0.010). Significantly higher levels of PTX3 were observed in patients on admission with ACLF (8.9
vs. 3.1
ng/mL; p ‹ 0.001) and MELD score ≥ 20 (6.6
vs. 3.4 ng/mL; p = 0.002). Death within 90 days occurred in 30.8% of patients and
was associated with higher levels of PTX3 (5.3
vs. 3.4 ng/mL; p = 0.009). The probability of Kaplan-Meier survival was 77.0% in
patients with PTX-3 ‹ 5.3 ng mL (upper tercile) and 53.5% in those with PTX3 ≥ 5.3 ng/mL (p = 0.002).
Conclusion. These results
indicate the potential for use of PTX3 as an inflammatory biomarker for the prognosis of patients with hepatic cirrhosis.
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