2018
DOI: 10.1111/1751-2980.12596
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Serum Wisteria floribunda agglutinin‐positive Mac‐2‐binding protein evaluates liver function and predicts prognosis in liver cirrhosis

Abstract: Serum WFA -M2BP is a reliable predictor of liver function and prognosis in LC and could be incorporated into clinical surveillance strategies for LC patients, especially those with HBV infection.

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Cited by 7 publications
(5 citation statements)
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References 49 publications
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“…M2BPGi level increases when compensated cirrhosis develops to decompensated cirrhosis [82][83][84]. Therefore, in patients with cirrhosis, high M2BPGi levels indicate a poor prognosis [82, 85, Fig.…”
Section: Utility Of M2bpgi In Cirrhosismentioning
confidence: 99%
See 1 more Smart Citation
“…M2BPGi level increases when compensated cirrhosis develops to decompensated cirrhosis [82][83][84]. Therefore, in patients with cirrhosis, high M2BPGi levels indicate a poor prognosis [82, 85, Fig.…”
Section: Utility Of M2bpgi In Cirrhosismentioning
confidence: 99%
“…M2BPGi levels increase as the disease progresses. M2BPGi can be used to assess disease status, such as that of liver fibrosis [31-38, 52-58, 71-75], HCC risk [31, 32, 36, 48-51, 53, 58, 62-69, 79, 104], HCC recurrence risk [92][93][94], liver function [82,[87][88][89][90][91], and prognosis of chronic liver diseases [82][83][84][85][86], with progression of the disease. In one relevant metaanalysis, the sensitivities and specificities for predicting significant fibrosis ( ≥ F2), advanced fibrosis ( ≥ F3), and cirrhosis were 0.690, 0.764, and 0.818 and 0.778, 0.758, and 0.839, respectively [21].…”
Section: Utility Of M2bpgi In Chronic Liver Diseasesmentioning
confidence: 99%
“…Recently, M2BPGi has been used for predicting cirrhosis-related outcomes. Published studies have demonstrated that M2BPGi (cutoff values ranged from 3.61 to 6.15 C.O.I) was an independent risk factor for liver-related mortality or all-cause mortality in cirrhotic patients [18,38,39]. Xu et al [39] retrospectively enrolled 197 cirrhotic patients over a median follow-up period of 23 months and showed that M2BPGi was an independent risk factor for liver-related death in patients with HBV infection and independently predicted clinical decompensation in compensated cirrhosis.…”
Section: Discussionmentioning
confidence: 99%
“…Published studies have demonstrated that M2BPGi (cutoff values ranged from 3.61 to 6.15 C.O.I) was an independent risk factor for liver-related mortality or all-cause mortality in cirrhotic patients [18,38,39]. Xu et al [39] retrospectively enrolled 197 cirrhotic patients over a median follow-up period of 23 months and showed that M2BPGi was an independent risk factor for liver-related death in patients with HBV infection and independently predicted clinical decompensation in compensated cirrhosis. In our previous study which enrolled 48 patients with portal hypertension confirmed by HVPG measurement, we found that plasma M2BPGi values correlated with HVPG levels and helped to predict bacterial infections, with cutoff value of 6 C.O.I [19].…”
Section: Discussionmentioning
confidence: 99%
“…Additionally, previous studies have demonstrated that plasma M2BPGi levels were higher in patients with decompensated cirrhosis and higher plasma M2BPGi level was an independent risk factor for liver-related mortality or all-cause mortality in cirrhotic patients [ 21 24 ]. Nevertheless, in our studies, we found that M2BPGi did not show a predictive value for all-cause mortality and occurrence of cirrhosis-related complications, including SBP, hepatic encephalopathy, variceal bleeding, hepatorenal syndrome during the follow-up period.…”
Section: Discussionmentioning
confidence: 99%