Evidence map›Paper›PMID 33412574›Full record

ArticlePloS one2021

Interleukin-18 and interferon-γ single nucleotide polymorphisms in Egyptian patients with tuberculosis.

Noha A Hassuna, Mohamed El Feky, Aliae A R Mohamed Hussein, Manal A Mahmoud, Naglaa K Idriss, Sayed F Abdelwahab, Maggie A Ibrahim

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Multiple CD59 Polymorphisms in Chinese Patients withJournal of immunology research · 2023
    Article
  7. Research progress on genetic control of host susceptibility to tuberculosis.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2022
    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

7 authors at 3 institutions in 2 countries.

Noha A HassunaDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Minia University, Minia, Egypt.ORCID 0000-0001-6702-2341
Mohamed El FekyDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Assiut University, Assiut, Egypt.
Aliae A R Mohamed HusseinDepartment of Chest Diseases and Tuberculosis, Faculty of Medicine, Assiut University, Assiut, Egypt.
Manal A MahmoudDepartment of Chest Diseases and Tuberculosis, Faculty of Medicine, Assiut University, Assiut, Egypt.
Naglaa K IdrissDepartment of Medical Biochemistry, Faculty of Medicine, Assiut University, Assiut, Egypt.
Sayed F AbdelwahabDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Minia University, Minia, Egypt.ORCID 0000-0002-9636-7485
Maggie A IbrahimDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Assiut University, Assiut, Egypt.
Assiut University · EGMinia University · EGTaif University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterleukin-18 (IL-18) and interferon-γ (IFN-γ) are cytokines of crucial role in inflammation and immune reactions. There is a growing evidence supporting important roles for IL-18 and IFN γ in tuberculosis (TB) infection and anti-tuberculosis immunity.

objectiveTo evaluate the role of polymorphisms in IL-18-607 and -137 and INF-γ +874 in susceptibility to TB infection among Egyptian patients.

methodsA case control study was conducted to investigate the polymorphism at IL-18-607, -137 and INF-γ+874 by sequence specific primer-polymerase chain reaction (SSP- PCR) in 105 patients with pulmonary and extra pulmonary tuberculosis and 106 controls.

resultsA significant protective effect against TB was found in homozygous CC genotype at IL-18 -137G/C, in addition to a 7-fold risk with GG and GC genotypes in the recessive model. Apart from a decreased risk with the AC genotype, no association was detected between the susceptibility to TB and different genotypes or alleles at the IL-18 -607A/C site. The homozygous AA genotype in INF-γ+874 showed a significant higher risk to TB than the homozygous TT or heterozygous AT genotypes with nearly a 2-fold risk of TB infection with the A allele. Regarding haplotype association, the GC haplotype was strongly associated with TB infection compared to other haplotypes.

conclusionThese findings suggest; for the first time in Egypt; a significant risk to TB infection with SNP at the IL-18-137G/C with no LD with SNP at the IL-18-607 site. The homozygous AA genotype in INF-γ+874 showed a significant higher risk to TB than the homozygous TT or heterozygous AT genotypes.

Indexed as

Genetic Predisposition to DiseaseGenotypeAdultAllelesAntitubercular AgentsCase-Control StudiesEgyptFemaleGene FrequencyHumansInterferon-gammaInterleukin-18MaleMiddle AgedPolymorphism, Single NucleotideTuberculosisAntitubercular AgentsInterferon-gammaInterleukin-18

Identifiers

PMID33412574
PMCPMC7790531
OpenAlexW3118479834

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.