Usefulness of Mac-2 Binding Protein Glycosylation Isomer for Prediction of Posthepatectomy Liver Failure in Patients With Hepatocellular Carcinoma

OBJECTIVE: The aim of this study was to evaluate the usefulness of the Mac-2 binding protein glycosylation isomer (M2BPGi) for the prediction of posthepatectomy liver failure (PHLF) in hepatocellular carcinoma (HCC) patients.

SUMMARY BACKGROUND DATA: M2BPGi is a novel serum marker of liver fibrosis. The usefulness of M2BPGi for the prediction of PHLF has not been evaluated.

METHODS: Clinicopathological data were analyzed in 138 HCC patients who underwent liver resection between August 2011 and November 2014. PHLF was evaluated according to the definition of the International Study Group of Liver Surgery. Performance of preoperative parameters in predicting PHLF was determined using receiver operating characteristic (ROC) analysis.

RESULTS: Serum M2BPGi level correlated with the METAVIR fibrosis score. M2BPGi levels of hepatitis C virus (HCV)-positive patients were significantly higher than those of HCV-negative patients, even in the same fibrosis stage. PHLF ≥ Grade B developed in 19 patients (13.8%). The area under the ROC curve (AUROC) of M2BPGi for the prediction of PHLF ≥ Grade B was 0.71. In multivariate analysis, M2BPGi [odds ratio (OR): 2.08, 95% confidence interval (CI) 1.28-3.55], platelet count (OR: 0.39, 95% CI 0.18-0.80), and resection rate (OR: 2.71, 95% CI 1.46-5.40) were the significant factors associated with PHLF ≥ Grade B. The AUROC of the PHLF index defined by these factors was 0.81. Notably, in patients with HCV infection, the predictive ability of M2BPGi for PHLF (AUROC 0.85) was the best among the preoperative parameters.

CONCLUSIONS: M2BPGi is a useful predictor of PHLF, especially in patients with HCV infection.

Medienart:

E-Artikel

Erscheinungsjahr:

2017

Erschienen:

2017

Enthalten in:

Zur Gesamtaufnahme - volume:265

Enthalten in:

Annals of surgery - 265(2017), 6 vom: 28. Juni, Seite 1201-1208

Sprache:

Englisch

Beteiligte Personen:

Okuda, Yukihiro [VerfasserIn]
Taura, Kojiro [VerfasserIn]
Yoshino, Kenji [VerfasserIn]
Ikeno, Yoshinobu [VerfasserIn]
Nishio, Takahiro [VerfasserIn]
Yamamoto, Gen [VerfasserIn]
Tanabe, Kazutaka [VerfasserIn]
Koyama, Yukinori [VerfasserIn]
Hatano, Etsuro [VerfasserIn]
Tanaka, Shiro [VerfasserIn]
Uemoto, Shinji [VerfasserIn]

Links:

Volltext

Themen:

8013-11-4
8063-16-9
Antigens, Neoplasm
Biomarkers
Drug Combinations
Journal Article
Membrane Glycoproteins
Perdiem
Psyllium
Senna Extract
TAA90K protein, human

Anmerkungen:

Date Completed 20.07.2017

Date Revised 08.04.2022

published: Print

Citation Status MEDLINE

doi:

10.1097/SLA.0000000000001836

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM261866729