Evidence map›Paper›PMID 25837166›Full record

ArticleYonsei medical journal2015

IL28B is associated with outcomes of chronic HBV infection.

Xiaodong Shi, Xiumei Chi, Yu Pan, Yanhang Gao, Wanyu Li, Chen Yang, Jin Zhong, Damo Xu, Manna Zhang, Gerald Minuk and 2 more

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
0.3field-weighted citation impact, top 39% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. The Association ofInternational journal of molecular sciences · 2024
    Article
  4. Review
  5. Article
  6. Review
  7. Association between interleukin-10 gene promoter polymorphisms and susceptibility to liver cirrhosis.International journal of clinical and experimental pathology · 2015
    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

12 authors at 6 institutions in 3 countries.

Xiaodong ShiDepartment of Hepatology, First Hospital of Jilin University, Changchun, China.
Xiumei ChiDepartment of Hepatology, First Hospital of Jilin University, Changchun, China.
Yu PanDepartment of Hepatology, First Hospital of Jilin University, Changchun, China.
Yanhang GaoDepartment of Hepatology, First Hospital of Jilin University, Changchun, China.
Wanyu LiDepartment of Hepatology, First Hospital of Jilin University, Changchun, China.
Chen YangInstitute Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, China.
Jin ZhongInstitute Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, China.
Damo XuInstitute of Infection, Immunity and Inflamm, University of Glasgow, Glasgow, UK.
Manna ZhangSection of Hepatology, University of Manitoba, Winnipeg, Canada.
Gerald MinukSection of Hepatology, University of Manitoba, Winnipeg, Canada.
Jing JiangDepartment of Clinical Epidemiology, First Hospital of Jilin University, Changchun, China. jiangjing19702000@yahoo.cn.
Junqi NiuDepartment of Hepatology, First Hospital of Jilin University, Changchun, China. junqiniu2013@aliyun.com.
Jilin University · CNFirst Hospital of Jilin University · CNUniversity of Manitoba · CAChinese Academy of Sciences · CNInstitute of Infection and Immunity · CAInstitut Pasteur of Shanghai · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe role of IL28B gene variants and expression in hepatitis B virus (HBV) infections are not well understood. Here, we evaluated whether IL28B gene expression and rs12979860 variations are associated with HBV outcomes. MATERIALS AND

methodsIL28B genetic variations (rs12979860) were genotyped by pyrosequencing of DNA samples from 137 individuals with chronic HBV infection [50 inactive carriers (IC), 34 chronic hepatitis B (CHB), 27 cirrhosis, 26 hepatocellular carcinoma (HCC)], and 19 healthy controls. IL28A/B mRNA expression in peripheral blood mononuclear cells was determined by qRT-PCR, and serum IL28B protein was measured by ELISA.

resultsPatients with IL28B C/C genotype had greater IL28A/B mRNA expression and higher IL28B protein levels than C/T patients. Within the various disease stages, compared to IC and healthy controls, IL28B expression was reduced in the CHB, cirrhosis, and HCC cohorts (CHB vs. IC, p=0.02; cirrhosis vs. IC, p=0.01; HCC vs. IC, p=0.001; CHB vs. controls, p<0.01; cirrhosis vs. controls, p<0.01; HCC vs. controls, p<0.01). When stratified with respect to serum HBV markers in the IC and CHB cohorts, IL28B mRNA and protein levels were higher in HBeAg-positive than negative individuals (p=0.01). Logistic regression analysis revealed that factors associated with high IL28B protein levels were C/C versus C/T genotype [p=0.016, odds ratio (OR)=0.25, 95% confidence interval (CI)=0.08-0.78], high alanine aminotransferase values (p<0.001, OR=8.02, 95% CI=2.64-24.4), and the IC stage of HBV infection (p<0.001).

conclusionOur data suggest that IL28B genetic variations may play an important role in long-term development of disease in chronic HBV infections.

Indexed as

AdultAgedAlanine TransaminaseAsian PeopleBiomarkersCarcinoma, HepatocellularCase-Control StudiesChinaDNA, ViralEnzyme-Linked Immunosorbent AssayFemaleGenotypeHepatitis B, ChronicHepatitis B virusHumansInterferon LambdaAlanine TransaminaseBiomarkersDNA, ViralInterferon Lambdainterferon-lambda, humanInterferonsInterleukinsRNA, Messengercirrhosisgenetic variationHepatitis B virushepatocellular carcinomainterleukin 28B

Identifiers

PMID25837166
PMCPMC4397430
OpenAlexW2064969668

What OpenQuestion holds

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LicenceCC BY-NC
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.