Evidence map›Paper›PMID 33063838›Full record

ArticleHistology and histopathology2020

Plasma Golgi protein 73 levels predict prognosis of HCV-related hepatic fibrosis.

Lingdi Liu, Zaid Al-Dhamin, Xiwei Yuan, Luyao Cui, Yang Yang, Wen Zhao, Ying Zhang, Na Fu, Yuemin Nan

Abstract read
PubMed Publisher
In one paragraph

Article in Histology and histopathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. [Diagnostic value of novel hepatic fibrosis markers in assessing cirrhosis in patients with chronic hepatitis C].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Lingdi Liu *Department of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China.
Zaid Al-Dhamin *Department of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China.
Xiwei YuanDepartment of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China.
Luyao CuiDepartment of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China.
Yang YangDepartment of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China.
Wen ZhaoDepartment of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China.
Ying ZhangDepartment of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China.
Na FuDepartment of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China.
Yuemin NanDepartment of Traditional and Western Medical Hepatology, Third Hospital of Hebei Medical University and Hebei Key Laboratory of Mechanism of Liver Fibrosis in Chronic Liver Disease, Shijiazhuang, China. nanyuemin@163.com.
Hebei Medical University · CN

Funding

Government-funded clinical talents project of Hebei province (2016), National Natural Science Foundation of China 81700525Key Research and Development Program of Hebei Province 19277779DNatural Science Foundation of Hebei Province H2018206384
6 · The paper itself

Abstract

objectivesTo explore the correlation between plasma Golgi protein 73 (GP73) and progression of hepatitis C virus (HCV)-induced hepatic fibrosis.

methodsA total of 232 subjects of chronic hepatitis C and 31 healthy controls were enrolled from the Third Hospital of Hebei Medical University from January 2010 to September 2018. The plasma GP73 levels were detected by ELISA. Liver tissue sections stained with hematoxylin and eosin and Masson-trichrome were examined under a light microscope based on the METAVIR scoring system and "Beijing classification (P-I-R)". The correlation analysis and receiver operating characteristic (ROC) curve were performed to analyze the diagnostic efficiency of plasma GP73, APRI, and FIB-4 for staging hepatic fibrosis and predicting the disease progression.

resultsThe plasma GP73 levels were increased with the progression of liver fibrosis, and GP73 concentrations in healthy controls, HCV patients with fibrosis stage 1, 2, 3 and 4 were 94.82, 151.3, 157.9, 181.7 and 208.5 ng/ml, respectively. According to "Beijing classification", There was a statistically significant difference in plasma GP73 concentrations between patients in the progression and regressive / indeterminate group (177.08 vs 154.00 ng/ml , P = 0.007).The area under the ROC curves (AUCs) of GP73, APRI, and FIB-4 for diagnosis of liver cirrhosis were 0.89, 0.77, and 0.82, respectively, and GP73 for progressive fibrosis was 0.73. The plasma GP73 levels were significantly positively correlated with hepatic inflammation, serum ALT, and negatively correlated with albumin levels.

conclusionThe plasma GP73 might be a potential biomarker for staging liver fibrosis, and could predict regression or progression of HCV-related liver fibrosis.

Indexed as

AdultAgedBiomarkersBiopsyDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleHepatitis C, ChronicHumansLiver CirrhosisMaleMembrane ProteinsMiddle AgedPredictive Value of TestsPrognosisRetrospective StudiesBiomarkersGOLM1 protein, humanMembrane Proteins

Identifiers

PMID33063838
OpenAlexW3093413175

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.