Evidence map›Paper›PMID 39103590›Full record

ArticleInflammation2025

MiR-146a (rs2910164) Gene Polymorphism and Its Impact on Circulating MiR-146a Levels in Patients with Inflammatory Bowel Diseases.

Rasha Ahmed Ghorab, Shaimaa H Fouad, Ahmed F Sherief, Eman M El-Sehsah, Sara Shamloul, Sara I Taha

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Article in Inflammation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rasha Ahmed GhorabDepartment of Clinical Pathology, Faculty of Medicine, Ain-Shams University, 11591 Abbasia, Cairo, Egypt.
Shaimaa H FouadDepartment of Internal Medicine /Allergy and Clinical Immunology, Faculty of Medicine, Ain-Shams University, Cairo, Egypt.
Ahmed F SheriefDepartment of Tropical Medicine, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Eman M El-SehsahDepartment of Medical Microbiology and Immunology, Mansoura Faculty of Medicine, Mansoura, Egypt.
Sara ShamloulDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Sara I TahaDepartment of Clinical Pathology, Faculty of Medicine, Ain-Shams University, 11591 Abbasia, Cairo, Egypt. dr_sara_ib@med.asu.edu.eg.ORCID http://orcid.org/0000-0001-8224-8701

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA-146a (miR-146a) has been involved in the pathophysiology of inflammatory bowel disease (IBD). However, the precise processes are still not entirely understood. Contradictory studies suggest that miR-146a expression could be influenced by the miR-146a rs2910164 C > G polymorphism. This case-control study aimed to investigate the association of miR-146a rs2910164 C > G gene polymorphism and its impact on circulating miR-146a expression levels in Egyptian IBD patients. We included 40 IBD patients and 30 matched healthy controls. Genotyping of miR-146a rs2910164 polymorphism and assessment of miR-146a expression level were done using quantitative real-time PCR in all participants. MiR-146a rs2910164 GG genotype and the G allele were reported in 47% and 70% of the IBD patient group, respectively. And they were associated with increased IBD risk. All the IBD patients with the CC genotype (100%) and most of those with the CG genotype (66.67%) had an inactive disease, while most IBD patients with the GG genotype (73.68%) had an active disease. The miR-146a expression level was the highest with the CC genotype and the lowest with the GG genotype. Also, miR-146a expression level decreased significantly in IBD patients than controls and with disease activity. Combined detection of fecal calprotectin with miR-146a expression level improved the diagnostic sensitivity and the negative predictive value in differentiating IBD patients with active disease from those inactive. Our study identified a strong association of miR-146a rs2910164 GG genotype and G allele with IBD-increased susceptibility and activity in the Egyptian population. The miR-146a rs2910164 polymorphism can reduce miR-146a expression levels in these patients as well. Further research on a larger sample size and different ethnic populations can be the key to progress in establishing this genetic association.

Indexed as

Inflammatory Bowel DiseasesMicroRNAsPolymorphism, Single NucleotideAdultCase-Control StudiesEgyptFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedMicroRNAsMIRN146 microRNA, humanactivityCrohn’s diseaseinflammatory bowel diseasemicroRNApolymorphismulcerative colitis

Identifiers

PMID39103590
PMCPMC12234608

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