Evidence map›Paper›PMID 36172689›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2022

Interleukin-10-1082A>G (rs1800896) Single Nucleotide Polymorphism is Not a Risk Factor of Chronic Lymphocytic Leukemia in Sudanese Population.

Ameen Abdulaziz Basabaeen, Enaam Abdelrhman Abdelgader, Ebtihal Babekir Ahmed, Nour Mahmoud Abdelateif, Sadia Osman Abdelrahim, Omnia Mohamed Sharif, Osama Ali Altayeb, Eman Abbass Fadul, Ibrahim Osman Ibrahim

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

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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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Analysis of Mutational Status ofInternational journal of molecular sciences · 2024
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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

9 authors at 2 institutions in 2 countries.

Ameen Abdulaziz BasabaeenDepartment of Hematology, Faculty of Medical Laboratory Sciences, Al Neelain University, Khartoum, Sudan.ORCID 0000-0003-0958-5212
Enaam Abdelrhman AbdelgaderDepartment of Pathology, Faculty of Medicine, Al Neelain University, Khartoum, Sudan.
Ebtihal Babekir AhmedDepartment of Hematology, Faculty of Medical Laboratory Sciences, Al Neelain University, Khartoum, Sudan.
Nour Mahmoud AbdelateifDepartment of Hematology, Faculty of Medical Laboratory Sciences, Al Neelain University, Khartoum, Sudan.
Sadia Osman AbdelrahimDepartment of Hematology, Faculty of Medical Laboratory Sciences, Al Neelain University, Khartoum, Sudan.
Omnia Mohamed SharifDepartment of Haematology, Faculty of Medical Laboratory Sciences, Sudan University of Science and Technology, Khartoum, Sudan.
Osama Ali AltayebFlow Cytometry Laboratory for Leukemia & Lymphoma Diagnosis, Khartoum, Sudan.
Eman Abbass FadulFlow Cytometry Laboratory for Leukemia & Lymphoma Diagnosis, Khartoum, Sudan.
Ibrahim Osman IbrahimDepartment of Hematology, Faculty of Medical Laboratory Sciences, Al Neelain University, Khartoum, Sudan.ORCID 0000-0002-8223-5369
Al-Neelain University · SDHadhramout University · YE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe present study was conducted to examine the association between the IL-10-1082A>G (rs 1800896) polymorphism and risk of Chronic Lymphocytic Leukemia and to assess the correlation between this polymorphism and clinicopathological characters.

methodsA case-control study was conducted in Khartoum state, Sudan, during the period from April 2017 to April 2018, involved 110 CLL patients and 80 healthy volunteers as a control group. Physical examination, complete blood count, and immunophenotype were performed in all patients to confirm the diagnosis. Clinical staging such as Rai and Binet were studied. CD38 and ZAP70 were performed by flow cytometry. Blood samples were collected from all participants; DNA was extracted by using ANALYTIKJENA Blood DNA Extraction Kit and analyzed IL-10-1082A>G polymorphism by using Allele Specific-Polymerase Chain Reaction. The statistical analysis was performed using statistical  package  for  social  sciences  version 23.0 software.

resultsFrequency of AA, AG, and GG genotypes was 32.7%, 55.5%, and 11.8% for the patient group and 31.25%, 51.25%, and 17.5% in the control group, respectively. The genotype of IL-10 (-1082A>G) did not associate with susceptibility of CLL in our population. The study showed that the G allele of the IL-10 gene (-1082A>G) is associated with the male sex. However, no significant association was found between -1082A>G genotype and clinicopathological characters.

conclusionOur results do not support the involvement of the IL-10 -1082A>G promoter gene polymorphism in the increased CLL susceptibility. IL-10-1082G allele (IL-10-1082AG or IL-10-1082GG) was found more frequently in males. Furthermore, no association was observed between the IL-10-1082A>G polymorphism and clinical stages systems as well as established poor prognostic markers. Finally, within the group of patients with CLL, there was no difference in the age at diagnosis and hematological parameters according to genotype distributions.

Indexed as

Interleukin-10Leukemia, Lymphocytic, Chronic, B-CellPolymorphism, Single NucleotideCase-Control StudiesGenetic Predisposition to DiseaseGenotypeHumansMaleRisk FactorsIL10 protein, humanInterleukin-10CLLIL-1082A> GInterleukin-10Single nucleotide polymorphism

Identifiers

PMID36172689
PMCPMC9810308
OpenAlexW4298007533

What OpenQuestion holds

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LicenceCC BY-NC
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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.