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Plasminogen as a prognostic biomarker for HBV-related acute-on-chronic liver failure
Daxian Wu, … , Zeyu Sun, Lanjuan Li
Daxian Wu, … , Zeyu Sun, Lanjuan Li
Published March 16, 2020
Citation Information: J Clin Invest. 2020;130(4):2069-2080. https://doi.org/10.1172/JCI130197.
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Clinical Research and Public Health Hepatology

Plasminogen as a prognostic biomarker for HBV-related acute-on-chronic liver failure

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Abstract

BACKGROUND HBV-related acute-on-chronic liver failure (HBV-ACLF) is hallmarked by high short-term mortality rates, calling for accurate prognostic biomarkers for initial risk stratification.METHODS Three tandem mass tag–labeled (TMT-labeled) quantitative proteomic studies were performed on 10 patients with HBV-related acute hepatic decompensation and on 20 patients with HBV-ACLF. Candidate biomarkers were preliminarily verified in a cross-sectional cohort (n = 144) and further confirmed in 2 prospective cohorts (n = 207 and n = 148).RESULTS Plasminogen, a potential prognostic biomarker for HBV-ACLF, was identified by TMT quantitative proteomics and preliminarily verified in the cross-sectional cohort. Further validation with a prospective cohort (n = 207) showed that plasminogen levels at admission were significantly lower (P < 0.001) in HBV-ACLF nonsurvivors than in survivors. The cumulative survival duration of patients with high plasminogen levels was significantly longer (P < 0.001) than that of patients with low plasminogen levels. During hospitalization, plasminogen levels significantly decreased (P = 0.008) in the deterioration group but significantly increased (P < 0.001) in the improvement group. Additionally, plasminogen levels gradually increased in survivors but gradually decreased in nonsurvivors. The P5 score, a prognostic panel incorporating plasminogen levels, hepatic encephalopathy occurrence, age, international normalized ratio (INR), and total bilirubin, was significantly superior to the Child-Pugh, Model for End-stage Liver Disease (MELD), Chronic Liver Failure Consortium ACLF (CLIF-C ACLF), Chinese Group on the Study of Severe Hepatitis B (COSSH), and HINT (a prognostic score based on hepatic encephalopathy occurrence, INR, neutrophil count, and thyroid-stimulating hormone) scores (all P < 0.05). The performances of the plasminogen level and P5 score were validated in a second multicenter, prospective cohort (n = 148).CONCLUSIONS Plasminogen is a promising prognostic biomarker for HBV-ACLF, and sequential plasminogen measurements could profile the clinical course of HBV-ACLF. P5 is a high-performance prognostic score for HBV-ACLF.FUNDING The National Key Research and Development Program (2017YFC1200204); the National Natural Science Foundation of China (81400589, 81600497); the Foundation for Innovative Research Groups of the National Natural Science Foundation of China (81121002); the Chinese High-Tech Research and Development Programs (2012AA020204); the National S&T Major Project (2012ZX10002004); and the Zhejiang Provincial Medicine and Health Science and Technology Project (2016147735).

Authors

Daxian Wu, Sainan Zhang, Zhongyang Xie, Ermei Chen, Qunfang Rao, Xiaoli Liu, Kaizhou Huang, Jing Yang, Lanlan Xiao, Feiyang Ji, Zhengyi Jiang, Yalei Zhao, Xiaoxi Ouyang, Danhua Zhu, Xiahong Dai, Zhouhua Hou, Bingjie Liu, Binbin Deng, Ning Zhou, Hainv Gao, Zeyu Sun, Lanjuan Li

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Figure 2

Bioinformatics analysis of proteomics data.

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Bioinformatics analysis of proteomics data.
(A) Venn diagram of the 3 TM...
(A) Venn diagram of the 3 TMT experiments. (B) Volcano plot of the 136 DEPs between AHD and ACLF patients. (C) Unsupervised clustering heatmap of the 136 DEPs between AHD and ACLF patients. Up, upregulated; Down, downregulated; Not, no change. (D) Prediction of upstream transcription factors related to DEPs. The value in parentheses indicates the percentage of proteins in the 136 DEPs predicted to be regulated by each TF, and the value in each sector indicates hypergeometric P value of the TF enrichment analysis. (E) Expression of HNF-1α in liver tissues. All patients with LC, AHD, or ACLF had an underlying HBV infection. BACH1, transcription regulator protein BACH1; PPARγ, peroxisome proliferator–activated receptor γ; FOXA1, hepatocyte nuclear factor 3-α; ESR2, estrogen receptor β; NR1H3, oxysterols receptor LXR-α.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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