Evidence map›Paper›PMID 29271328›Full record

ArticleEpidemiology and infection2018

Influence of IL28B and MxA gene polymorphisms on HCV clearance in Han Chinese population.

Feng Zang, Ming Yue, Yinan Yao, Mei Liu, Haozhi Fan, Yue Feng, Xueshan Xia, Peng Huang, Rongbin Yu

Open access · bronzeAbstract read
In one paragraph

Article in Epidemiology and infection, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Polymorphisms of theFrontiers in cellular and infection microbiology · 2023
    Article
  3. Virusdisease · 2019
    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 3 institutions in 1 country.

Feng ZangDepartment of Epidemiology and Biostatistics,Key Laboratory of Infectious Diseases, School of Public Health,Nanjing Medical University,Nanjing 211166,China.
Ming YueDepartment of Infectious Diseases,The First Affiliated Hospital of Nanjing Medical University,Nanjing 210029,China.
Yinan YaoDepartment of Epidemiology and Biostatistics,Key Laboratory of Infectious Diseases, School of Public Health,Nanjing Medical University,Nanjing 211166,China.
Mei LiuDepartment of Epidemiology and Biostatistics,Key Laboratory of Infectious Diseases, School of Public Health,Nanjing Medical University,Nanjing 211166,China.
Haozhi FanDepartment of Epidemiology and Biostatistics,Key Laboratory of Infectious Diseases, School of Public Health,Nanjing Medical University,Nanjing 211166,China.
Yue FengFaculty of Life Science and Technology,Kunming University of Science and Technology,Kunming 650500,China.
Xueshan XiaFaculty of Life Science and Technology,Kunming University of Science and Technology,Kunming 650500,China.
Peng HuangDepartment of Epidemiology and Biostatistics,Key Laboratory of Infectious Diseases, School of Public Health,Nanjing Medical University,Nanjing 211166,China.
Rongbin YuDepartment of Epidemiology and Biostatistics,Key Laboratory of Infectious Diseases, School of Public Health,Nanjing Medical University,Nanjing 211166,China.
Nanjing Medical University · CNKunming University of Science and Technology · CNJiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The high rate of chronic hepatitis C (CHC) was one of the key issues of global public health concern. Interferon (IFN)-λ relevant genes were in the antiviral treatment pathway, not only influenced hepatitis C virus (HCV) spontaneous clearance, but also affected the IFN-mediated viral clearance. The aim of this study was to identify the association of interleukin 28B (IL28B), myxovirus resistance A (MxA) gene polymorphisms with HCV spontaneous clearance and therapeutic response in Chinese CHC patients. IL28B and MxA gene genotypes were detected among 231 CHC carriers, 428 subjects with HCV spontaneous clearance and 662 CHC patients with pegylated IFN-α and ribavirin (pegIFN-α/RBV) treatment. Patients with MxA rs2071430 TT genotype were more likely to develop HCV infection chronicity (additive model: odds ratio (OR) 1.22, 95% confidence interval (CI) 1.01-1.48, P = 0.042). IL28B rs1298075 variant genotypes (additive model: OR 0.58, 95% CI 0.34-0.98, P = 0.040) and MxA rs17000900 variant genotypes (additive model: OR 0.54, 95% CI 0.30-0.99, P = 0.048) were less likely to achieve a sustained virological response. The life table indicated that patients with IL28B rs1298075 AG genotype were slower to achieve a viral load 106 copies/ml (all P < 0.05). This study illustrated that the carriage of IL28B rs12980275 AA had a positive effect on treatment response to pegIFN-α/RBV among Chinese CHC patients.

Indexed as

Polymorphism, GeneticChinaGenotypeHepacivirusHepatitis C, ChronicHumansInterferon LambdaInterferonsInterleukinsMyxovirus Resistance ProteinsSustained Virologic ResponseViral LoadInterferon Lambdainterferon-lambda, humanInterferonsInterleukinsMX1 protein, humanMyxovirus Resistance ProteinsChronic hepatitis CIL28BMxAspontaneous clearancetreatment response

Identifiers

PMID29271328
PMCPMC9134562
OpenAlexW2780933414

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.