Evidence map›Paper›PMID 30617966›Full record

SynthesisImmunologic research2019

Correlations between TLR polymorphisms and inflammatory bowel disease: a meta-analysis of 49 case-control studies.

Huijuan Wang, Shuhong Zhou, Jiahong Zhang, Shangwen Lei, Jing Zhou

Abstract readMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Immunologic research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Mediators of inflammation · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Huijuan WangDepartment of Immunology and Rheumatology, Gansu Provincial Hospital, No. 204 Donggang West Road, Lanzhou, 730000, Gansu, China. huijuanwang898@aliyun.com.
Shuhong ZhouDepartment of Immunology and Rheumatology, Gansu Provincial Hospital, No. 204 Donggang West Road, Lanzhou, 730000, Gansu, China.
Jiahong ZhangDepartment of Immunology and Rheumatology, Gansu Provincial Hospital, No. 204 Donggang West Road, Lanzhou, 730000, Gansu, China.
Shangwen LeiDepartment of Immunology and Rheumatology, Gansu Provincial Hospital, No. 204 Donggang West Road, Lanzhou, 730000, Gansu, China.
Jing ZhouDepartment of Immunology and Rheumatology, Gansu Provincial Hospital, No. 204 Donggang West Road, Lanzhou, 730000, Gansu, China.
Gansu Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, the roles of toll-like receptor (TLR) polymorphisms in inflammatory bowel disease (IBD) were intensively explored, with conflicting results. Therefore, we performed this study to better assess the relationship between TLR polymorphisms and the risk of IBD. Eligible studies were searched in PubMed, Medline, Embase, and Web of Science. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to estimate associations between TLR polymorphisms and IBD. Significant associations with the risk of IBD were detected for the TLR1 rs5743611, TLR4 rs4986790, TLR4 rs4986791, and TLR6 rs5743810 polymorphisms in overall analyses. Further subgroup analyses according to ethnicity of participants revealed that the TLR1 rs5743611, TLR4 rs4986790, TLR4 rs4986791, TLR6 rs5743810, and TLR9 rs352140 polymorphisms were significantly associated with the risk of IBD in Caucasians. Moreover, the TLR4 rs4986790 polymorphism was significantly correlated with the risk of IBD in West Asians, while the TLR9 rs352140 polymorphism was significantly associated with the risk of IBD in Africans. When we stratified available data according to type of disease, we found similar positive results for TLR1 rs5743611, TLR4 rs4986790, TLR4 rs4986791, and TLR6 rs5743810 polymorphisms. Our findings indicate that TLR1 rs5743611, TLR4 rs4986790, TLR4 rs4986791, TLR6 rs5743810, and TLR9 rs352140 polymorphisms may serve as genetic biomarkers of IBD in certain ethnicities. However, further well-designed studies are still warranted to confirm our findings.

Indexed as

BiomarkersGenetic Predisposition to DiseaseHumansInflammatory Bowel DiseasesPhenotypePolymorphism, GeneticPolymorphism, Single NucleotideRiskToll-Like ReceptorsBiomarkersToll-Like ReceptorsCrohn’s disease (CD)Gene polymorphismsInflammatory bowel disease (IBD)Meta-analysisToll-like receptor (TLR)Ulcerative colitis (UC)

Identifiers

PMID30617966
OpenAlexW2910650158

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.