Evidence map›Paper›PMID 30976740›Full record

ArticleHepatology communications2019

Mac-2 Binding Protein Glycosylation Isomer as a Hepatocellular Carcinoma Marker in Patients With Chronic Hepatitis B or C Infection.

Tomi Jun, Yao-Chun Hsu, Shintaro Ogawa, Yen-Tsung Huang, Ming-Lun Yeh, Cheng-Hao Tseng, Chung-Feng Huang, Chi-Ming Tai, Chia-Yen Dai, Jee-Fu Huang and 4 more

Abstract read
In one paragraph

Article in Hepatology communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

24 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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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

14 authors.

Tomi JunDepartment of Medicine Stanford University Medical Center Palo Alto CA.ORCID https://orcid.org/0000-0002-2120-1704
Yao-Chun HsuDivision of Gastroenterology and Hepatology Fu Jen Catholic University Hospital New Taipei Taiwan.
Shintaro OgawaDepartment of Virology and Liver Unit Nagoya City University Graduate School of Medical Sciences Nagoya Japan.
Yen-Tsung HuangInstitute of Statistical Science Academia Sinica Taipei Taiwan.
Ming-Lun YehHepatobiliary Division, Department of Internal Medicine Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung Taiwan.
Cheng-Hao TsengDivision of Gastroenterology and Hepatology E-Da Hospital Kaohsiung Taiwan.
Chung-Feng HuangHepatobiliary Division, Department of Internal Medicine Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung Taiwan.
Chi-Ming TaiGraduate Institute of Clinical Medical Science China Medical University Taichung Taiwan.
Chia-Yen DaiHepatobiliary Division, Department of Internal Medicine Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung Taiwan.
Jee-Fu HuangHepatobiliary Division, Department of Internal Medicine Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung Taiwan.
Wan-Long ChuangHepatobiliary Division, Department of Internal Medicine Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung Taiwan.
Ming-Lung YuHepatobiliary Division, Department of Internal Medicine Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung Taiwan.ORCID https://orcid.org/0000-0001-8145-1900
Yasuhito TanakaDepartment of Virology and Liver Unit Nagoya City University Graduate School of Medical Sciences Nagoya Japan.
Mindie H NguyenDivision of Gastroenterology and Hepatology Stanford University Medical Center Palo Alto CA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mac-2 binding protein glycosylation isomer (M2BPGi) is a novel glycoprotein biomarker that correlates with liver fibrosis. It has been investigated in East Asian populations as a hepatocellular carcinoma (HCC) biomarker. We assessed M2BPGi as an HCC biomarker in an ethnically diverse cohort of patients with chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infection. We enrolled 947 treatment-naive patients mono-infected with HBV or HCV without HCC at baseline. Biomarker levels were measured from baseline sera and correlated with longitudinal clinical data. The primary outcome was HCC occurrence during long-term follow-up. Median M2BPGi was significantly higher among patients with cirrhosis (2.67 versus 0.80;

Identifiers

PMID30976740
PMCPMC6442699

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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.