Evidence map›Paper›PMID 29270132›Full record

ArticleFrontiers in physiology2017

Discovery of a Potential Plasma Protein Biomarker Panel for Acute-on-Chronic Liver Failure Induced by Hepatitis B Virus.

Ni Zhou, Kuifeng Wang, Shanhua Fang, Xiaoyu Zhao, Tingting Huang, Huazhong Chen, Fei Yan, Yongzhi Tang, Hu Zhou, Jiansheng Zhu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Ni ZhouDepartment of Infectious Diseases, Affiliated Taizhou Hospital of Wenzhou Medical University, Taizhou, China.
Kuifeng WangDepartment of Infectious Diseases, Affiliated Taizhou Hospital of Wenzhou Medical University, Taizhou, China.
Shanhua FangE-Institute of Shanghai Municipal Education Committee, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Xiaoyu ZhaoDepartment of Infectious Diseases, Affiliated Taizhou Hospital of Wenzhou Medical University, Taizhou, China.
Tingting HuangDepartment of Infectious Diseases, Affiliated Taizhou Hospital of Wenzhou Medical University, Taizhou, China.
Huazhong ChenDepartment of Infectious Diseases, Affiliated Taizhou Hospital of Wenzhou Medical University, Taizhou, China.
Fei YanDepartment of Infectious Diseases, Affiliated Taizhou Hospital of Wenzhou Medical University, Taizhou, China.
Yongzhi TangDepartment of Infectious Diseases, Affiliated Taizhou Hospital of Wenzhou Medical University, Taizhou, China.
Hu ZhouE-Institute of Shanghai Municipal Education Committee, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Jiansheng ZhuDepartment of Infectious Diseases, Affiliated Taizhou Hospital of Wenzhou Medical University, Taizhou, China.
Wenzhou Medical University · CNChinese Academy of Sciences · CNShanghai Institute of Materia Medica · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis B virus (HBV)-associated acute-on-chronic liver failure (HBV-ACLF), characterized by an acute deterioration of liver function in the patients with chronic hepatitis B (CHB), is lack of predicting biomarkers for prognosis. Plasma is an ideal sample for biomarker discovery due to inexpensive and minimally invasive sampling and good reproducibility. In this study, immuno-depletion of high-abundance plasma proteins followed by iTRAQ-based quantitative proteomic approach was employed to analyze plasma samples from 20 healthy control people, 20 CHB patients and 20 HBV-ACLF patients, respectively. As a result, a total of 427 proteins were identified from these samples, and 42 proteins were differentially expressed in HBV-ACLF patients as compared to both CHB patients and healthy controls. According to bioinformatics analysis results, 6 proteins related to immune response (MMR), inflammatory response (OPN, HPX), blood coagulation (ATIII) and lipid metabolism (APO-CII, GP73) were selected as biomarker candidates. Further ELISA analysis confirmed the significant up-regulation of GP73, MMR, OPN and down-regulation of ATIII, HPX, APO-CII in HBV-ACLF plasma samples (

Indexed as

biomarkerCHBHBV-ACLFiTRAQproteomics

Identifiers

PMID29270132
PMCPMC5724358
OpenAlexW2774866263

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.