Evidence map›Paper›PMID 26626589›Full record

ArticleBMC infectious diseases2015

The variations of IL-23R are associated with susceptibility and severe clinical forms of pulmonary tuberculosis in Chinese Uygurs.

Daobin Jiang, Atikaimu Wubuli, Xin Hu, Syed Ikramullah, Abudoujilili Maimaiti, Wenbao Zhang, Qimanguli Wushouer

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2015. 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
1.2field-weighted citation impact, top 22% 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, 24 citations in OpenAlex.

  1. Article
  2. Article
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  7. Genetics and evolution of tuberculosis pathogenesis: New perspectives and approaches.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2020
    Review
  8. Oncotarget · 2018
    Article
  9. Article
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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

7 authors at 2 institutions in 1 country.

Daobin JiangDepartment of Pulmonology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China. fangxueer1027@163.com.
Atikaimu WubuliDepartment of Pulmonology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China. 492242282@qq.com.
Xin HuDepartment of Pulmonology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China. 147951422@qq.com.
Syed IkramullahDepartment of Pulmonology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China. dr.ikram96@yahoo.com.
Abudoujilili MaimaitiDepartment of Pulmonology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China. 276576643@qq.com.
Wenbao ZhangClinical Medical Research Institute, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830054, China. wenbaozhang2013@163.com.
Qimanguli WushouerDepartment of Pulmonology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China. qimenw@hotmail.com.
First Affiliated Hospital of Xinjiang Medical University · CNXinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence of tuberculosis (TB) remains high among Chinese Uygurs (a long-dwelling ethnic minority in Xinjiang) in China and the variants in IL-23R likely contribute to individual's diversity in host response during infection.

methodsA hospital based one to one matched case-control study was performed to assess the role of single nucleotide polymorphisms (SNPs) and copy number variation (CNV) of IL-23R in susceptibility and clinical features of pulmonary TB in Chinese Uygurs. Thirteen SNPs in IL-23R were genotyped by multiplex SNaPshot and a CNV was analyzed using Taqman real-time PCR in 250 pairs of pulmonary TB patients and controls.

resultsThe SNP rs7518660 (OR = 4.78, 95% CI 3.14-8.52) and the CNV in IL23R (OR = 2.75, 95% CI 1.51-4.98) were significantly associated with susceptibility to pulmonary TB. The SNP rs11465802 (OR = 3.23, 95% CI 1.85-5.62) was significantly associated with drug-resistance and the SNP rs1884444 (OR = 3.61, 95% CI 1.90-6.85) was significantly related to cavitary lesion in Chinese Uygurs.

conclusionsOur study shows for the first time that SNP and CNV in IL23R were associated with susceptibility, drug resistance and cavity formation of pulmonary TB. Our findings indicate that these IL-23R polymorphisms may be considered as risk factors for active pulmonary TB and its severe clinical forms.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAgedAsian PeopleCase-Control StudiesChinaDNA Copy Number VariationsEthnicityFemaleGene FrequencyGenetic Predisposition to DiseaseHumansMaleMiddle AgedReal-Time Polymerase Chain ReactionIL23R protein, humanReceptors, Interleukin

Identifiers

PMID26626589
PMCPMC4665827
OpenAlexW2187313729

What OpenQuestion holds

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LicenceCC BY
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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.