Evidence map›Paper›PMID 32912361›Full record

SynthesisEpidemiology and infection2020

Association of TLR3 (rs3775291) and IL-10 (rs1800871) gene polymorphisms with susceptibility to Hepatitis B infection: A meta-analysis.

Susu Ye, Xinlei Zhang, Yu Bao Zhang, Xintao Tian, Ailing Liu, Changxing Cui, Lei Shi, Di Xia

Abstract readMeta-Analysis
In one paragraph

Synthesis in Epidemiology and infection, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Association ofFrontiers in neuroscience · 2023
    Article
  7. Analysis of associations between theFrontiers in cellular and infection microbiology · 2023
    Article
  8. Article
  9. Article
  10. Review
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

8 authors.

Susu YeLiver Disease Center, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Xinlei ZhangDepartment of Medical Engineering, The 971st Hospital of the PLA, Qingdao, Shandong, China.
Yu Bao ZhangDepartment of Emergency, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Xintao TianDepartment of Emergency, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Ailing LiuDepartment of Gastroenterology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Changxing CuiDepartment of Emergency, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Lei ShiDepartment of Emergency, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Di XiaDepartment of Emergency, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.ORCID 0000-0001-6065-2543

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TLR3 and IL-10 play a crucial role in antiviral defence. However, there is a controversy between TLR3 rs3775291 and IL-10 rs1800871 polymorphisms and the risk of hepatitis B virus (HBV) infection. The purpose of this study is to explore the relationship between the two single nucleotide mutations and the risk of HBV infection by meta-analysis. Medline, EMBASE, Web of Science, CNKI, China Wanfang database were searched for the case-control studies on the relationship between TLR3 rs3775291 and IL-10 rs1800871 polymorphism and susceptibility to HBV, updated to June 2020. The data were analysed by Stata 15.0 software. A total of 22 articles were included. The results showed that in the analysis of IL10 rs1800871 polymorphism and the risk of HBV infection, the pooled OR was 1.21 (95% CI 1.06-1.37), 1.28 (95% CI 1.04-1.56) and 1.20 (95% CI 1.06-1.37) and 1.40 (95% CI 1.07-1.83) in the allele model (C vs. T), dominant model (CC+CT vs. TT), recessive model (CC vs. CT+TT) and homozygous model (CC vs. TT), respectively. There was no statistical significance in the heterozygote model. A subgroup analysis of the Asian population showed similar results. The analysis of TLR3 rs3775291 polymorphism and the risk of HBV showed that in the allele model (T vs. C), the pooled OR was 1.30 (95% CI 1.05-1.61). Except for the recessive model, no significances were found in other genetic models. In conclusion, TLR3 rs3775291 and IL-10 rs1800871 polymorphisms are associated with the risk of HBV. Allele C and genotype CC at IL10 rs1800871 loci, as well as allele T and genotype TT at TLR rs3775291 loci, may increase susceptibility to Hepatitis B infection.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideHepatitis BHumansInterleukin-10Toll-Like Receptor 3IL10 protein, humanInterleukin-10TLR3 protein, humanToll-Like Receptor 3Hepatitis B virusInterleukin 10meta-analysispolymorphismToll-like receptor 3

Identifiers

PMID32912361
PMCPMC7557109

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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.