Evidence map›Paper›PMID 31728561›Full record

SynthesisInflammation research : official journal of the European Histamine Research Society ... [et al.]2020

Genetic association between IL23R rs11209026 and rs10889677 polymorphisms and risk of Crohn's disease and ulcerative colitis: evidence from 41 studies.

Yi Zhu, HongGang Jiang, ZhiHeng Chen, BoHao Lu, Jin Li, XuNing Shen

Abstract readMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
0.9field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Yi ZhuDepartment of Gastrointestinal Surgery, The Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China. zhuanwen456@163.com.
HongGang JiangDepartment of Gastrointestinal Surgery, The Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
ZhiHeng ChenDepartment of Gastrointestinal Surgery, The Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
BoHao LuDepartment of Gastrointestinal Surgery, The Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
Jin LiDepartment of Gastrointestinal Surgery, The Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
XuNing ShenDepartment of Gastrointestinal Surgery, The Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
Jiaxing University · CN

Funding

The Medical and Health Science and Technology Project of Zhejiang Province 2019KY214
6 · The paper itself

Abstract

objectiveIL23R plays an important role in the pathogenesis of inflammatory bowel disease (IBD). The IL23R rs11209026 and rs10889677 polymorphisms have been shown to be associated with the development of Crohn's disease (CD) and ulcerative colitis (UC). But the results were inconsistent and inconclusive. So, we aim to investigate the genetic association between rs11209026 and rs10889677 polymorphisms and UC and CD risk by a meta-analysis.

methodsLiterature search was conducted through PubMed, CNKI, and web of science databases. Pooled OR and 95% CI was used to assess the association between the allelic, dominant and recessive models of IL23R rs11209026 and rs10889677 polymorphisms and UC and CD risk.

results41 publications with 13,803 patients with CD and 17,446 controls, as well as 5876 patients with UC and 10,053 controls were included in the present study. All the genetic models of rs11209026 polymorphism significantly decrease CD and UC risk (except for the recessive model in UC) (p < 0.05). A subgroup analysis based on ethnicity showed that the allelic (p < 0.00001, OR = 0.65) and dominant models (p < 0.00001, OR = 0.61) of rs11209026 polymorphism were significantly associated with UC risk in Caucasians, but not in Asians (p > 0.05). In addition, the allelic (CD: p < 0.00001, OR = 1.34; UC: p < 0.00001, OR = 1.22) and dominant models (CD: p = 0.002, OR = 1.39; UC: p = 0.01, OR = 1.29), but not the recessive model of rs10889677 polymorphism significantly increase the risk of CD and UC (p > 0.05). A subgroup analysis showed that the genetic models of rs10889677 polymorphism were associated with CD risk in Caucasians (p < 0.05), but not in Asians (p > 0.05). The dominant model of rs10889677 polymorphism was associated with UC risk in Asians (p = 0.04, OR = 1.54), but not in Caucasians (p > 0.05).

conclusionsOur meta-analysis demonstrated that the rs11209026 polymorphism might be a protective factor against developing IBD, while the rs10889677 polymorphism might be a risk factor for IBD.

Indexed as

Colitis, UlcerativeCrohn DiseaseGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideReceptors, InterleukinRisk FactorsIL23R protein, humanReceptors, InterleukinCrohn’s diseaseIL23RMeta-analysisPolymorphismUlcerative colitis

Identifiers

PMID31728561
OpenAlexW2984929914

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.