Evidence map›Paper›PMID 40704442›Full record

ArticleThe Journal of international medical research2025

Association of TLR3 1337C/T and 1234C/T polymorphisms with chronic hepatitis B virus infection in Sudanese patients: A case-control study.

Khalid Elyass, Najem Aldin M Osman, Babbiker Mohammed Taher Gorish, Abdelsalam Ma Nail, Waha Ismail Yahia Abdelmula, Nadir Musa Khalil Abuzeid

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Article in The Journal of international medical research, 2025. 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.

Khalid ElyassDepartment of Microbiology, Faculty of Medical Laboratory Sciences, Omdurman Islamic University, Sudan.
Najem Aldin M OsmanDepartment of Microbiology, Faculty of Medical Laboratory Sciences, Omdurman Islamic University, Sudan.ORCID 0000-0002-0763-0334
Babbiker Mohammed Taher GorishDepartment of Microbiology, Faculty of Medical Laboratory Sciences, Omdurman Islamic University, Sudan.ORCID 0000-0002-0693-3181
Abdelsalam Ma NailDepartment of Internal Medicine, Faculty of Medicine, Omdurman Islamic University, Sudan.
Waha Ismail Yahia AbdelmulaInternational Joint Laboratory on Synthetic Biology and Biomass Biorefinery, Biofuels Institute, Jiangsu University, PR China.
Nadir Musa Khalil AbuzeidDepartment of Microbiology, Faculty of Medical Laboratory Sciences, Omdurman Islamic University, Sudan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveThis study aimed to investigate the association of TLR3 single-nucleotide polymorphisms 1337 C/T (rs3775290) and 1234 C/T (rs3775291) with the risk of chronic hepatitis B virus infection.MethodsThis case-control study enrolled 136 participants (66 patients with chronic hepatitis B virus infection (cases) and 70 healthy controls). TLR3 polymorphisms were genotyped using polymerase chain reaction-restriction fragment length polymorphism. Demographic/clinical data were collected via standardized questionnaires and analyzed using Statistical Package for Social Sciences (significance level: p < 0.05).ResultsFor TLR3 1337 C/T polymorphism, the CT genotype prevalence was significantly higher in cases (47.0%) than in controls (31.4%) (odds ratio = 0.42, 95% confidence interval: 0.20-0.87, p = 0.0187), while the CC genotype demonstrated protective effects (39.4% in cases vs. 62.9% in controls; odds ratio = 0.26, 95% confidence interval: 0.07-0.94, p = 0.0314). The C allele frequency showed significant between-group differences (odds ratio = 0.46, p = 0.0044). No associations were observed for 1234 C/T single-nucleotide polymorphism (p = 1.0). Biochemical analysis revealed significantly elevated alanine aminotransferase (p = 0.0044) and aspartate aminotransferase (p < 0.0001) levels in cases than in controls.ConclusionsRegarding TLR3 1337 C/T single-nucleotide polymorphism, the CT genotype increases the risk of chronic hepatitis B virus infection (odds ratio = 0.42), while the CC genotype demonstrates protective effects (odds ratio = 0.26) in Sudanese populations, suggesting its utility as a therapeutic target and prognostic marker. No 1234 C/T associations were observed.

Indexed as

Genetic Predisposition to DiseaseHepatitis B, ChronicHepatitis B virusPolymorphism, Single NucleotideToll-Like Receptor 3AdultAllelesCase-Control StudiesFemaleGene FrequencyGenetic Association StudiesGenotypeHumansMaleMiddle AgedSudanTLR3 protein, humanToll-Like Receptor 3chronic hepatitis Bgenetic susceptibilityrs3775290SudanTLR3 polymorphisms

Identifiers

PMID40704442
PMCPMC12322355

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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.