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TLR 9 (rs352140) gene polymorphism in Helicobacter pylori infection in children
Nashwa Farouk Mohamed1, Ola Galal Ali Behairy2, Hebatallah Emam Mohammed Ahmed3
1Pediatrics, Faculty of Medicine, Benha University, Benha, 15131, Egypt. nashwa.farouk@fmed.bu.edu.eg.
Insights
The Toll-like receptor 9 (TLR9) rs352140 gene polymorphism significantly increases H. pylori infection risk in children. Children with TT or CT genotypes face a higher hazard of infection and gastritis.
Area of Science:
- Genetics
- Immunology
- Pediatrics
Background:
- Helicobacter pylori (H. pylori) infection is common globally, often acquired in childhood.
- Inflammation associated with H. pylori infection can lead to various gastrointestinal issues.
Purpose of the Study:
- To investigate the association between Toll-like receptor 9 (TLR9) gene polymorphism (rs352140) and H. pylori infection in children.
- To determine if TLR9 rs352140 influences inflammation and gastritis risk in pediatric H. pylori cases.
Main Methods:
- Cross-sectional study of 100 children with dyspeptic symptoms undergoing upper endoscopy.
- Inclusion of 50 H. pylori-positive and 50 H. pylori-negative children as controls.
- Genotyping of TLR9 (rs352140) and correlation with H. pylori status and gastritis incidence.
Main Results:
- A significant difference in TLR9 rs352140 gene polymorphism was observed between H. pylori-positive and negative children.
- Higher frequencies of TT and CT genotypes, and the T allele, were found in H. pylori-positive children.
- Children with TT genotype had 7.9 times higher H. pylori hazard; CT genotype had 3.6 times higher hazard; T allele carriers had 2.3 times higher risk.
Conclusions:
- TLR9 rs352140 gene polymorphism is significantly associated with H. pylori infection susceptibility in children.
- The TT and CT genotypes, and the T allele of TLR9 rs352140, are linked to an increased risk of H. pylori infection and gastritis.
Abstract:
Most of the global populace is susceptible to Helicobacter pylori (H. pylori) infection, which typically manifests in childhood. This study aimed to identify the role of TLR9 (rs352140) gene in suppressing or promoting the inflammation related to H. pylori infection in children. This cross-sectional study enrolled 100 children with dyspeptic symptoms undergoing upper endoscopy, including 50 with confirmed H. pylori infection and 50 age- and sex-matched H. pylori-negative controls. All children undertook full history, complete clinical investigation, laboratory testing, upper digestive endoscopies and genotyping of TLR9 (rs352140). A statistically significant difference presented among H. pylori positive and H. pylori negative children as regards TLR rs352140 gene polymorphism, as patients have statistically higher frequencies of homozygous TT genotype, CT genotype and of variant T allele in contrast to H. pylori negative group. Hazard of H. pylori is 7.9 times higher in children with TT genotype and 3.6 times higher in children with CT genotype in contrast to children carrying CC genotype. Also, children carrying the altered T allele had a statistically higher risk of H. pylori, 2.3 times in contrast to those carrying C allele. TLR9 rs352140 gene polymorphism was correlated with of H. pylori infection and incidence of gastritis in children.
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