Evidence map›Paper›PMID 37202334›Full record

ArticleHematology, transfusion and cell therapy

IL-4Rα (rs1801275) A>G polymorphism in Egyptian immune thrombocytopenia (ITP) patients: a single center experience.

Mohamed Abdelkader Morad, Noha A Doudar, Nehad Tawfeek, Maha Yacoub, Taha Azoz, Doaa El Demerdash

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Article in Hematology, transfusion and cell therapy. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Mohamed Abdelkader MoradKasr Al-Ainy Hospital, Faculty of Medicine, Cairo University, Egypt.
Noha A DoudarBeni-Suef University Hospital, Faculty of Medicine, Beni-Suef University, Egypt.
Nehad TawfeekKasr Al-Ainy Hospital, Faculty of Medicine, Cairo University, Egypt.
Maha YacoubKasr Al-Ainy Hospital, Faculty of Medicine, Cairo University, Egypt.
Taha AzozFaculty of Medicine, Cairo University, Egypt.
Doaa El DemerdashKasr Al-Ainy Hospital, Faculty of Medicine, Cairo University, Egypt. Electronic address: dr_eldemerdash@kasralainy.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionChronic immune thrombocytopenia (cITP) is characterized by dysregulation of the immune response. Until recently, the role of Th2-related cytokine gene polymorphisms was unclear. Interleukin 4 (IL-4) exerts its functions by binding to three types of IL-4 receptor (IL-4R) complexes. We aimed to explore the potential association between the gene polymorphism of IL-4Rα and cITP.

methodsWe investigated the clinical impact of the IL-4Rα (rs1801275) A>G single nucleotide polymorphism (SNP) using the polymerase chain reaction (PCR) followed by the restriction fragment length polymorphism (RFLP) method in 82 cITP patients and 60 healthy controls (HCs).

resultsThe IL-4Rα (rs1801275) A>G polymorphism analysis showed the mutant GG genotype was significantly higher in control females (p = 0.033). The wild AA genotype had a higher bleeding score (p = 0.02) in the adulthood onset group. Furthermore, the wild AA genotype in the cITP childhood onset group was significantly associated with the disease severity, as well as the response to treatment (p = 0.040).

conclusionThe mutant G allele is protective against the susceptibility to cITP in the Egyptian females. The IL-4Rα (rs1801275) A>G polymorphism may affect the clinical severity of cITP and treatment response in the Egyptian population.

Indexed as

IL4Immune thrombocytopenic purpuraTh2 cells, Cytokine receptor

Identifiers

PMID37202334
PMCPMC11451371

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