AI Article Synopsis

  • This study explored the link between a specific genetic variation (rs3804099) in a gene related to immune response and its impact on amebiasis infections in Lebanese children.
  • It included 180 participants, with 68 diagnosed with amebiasis, and utilized advanced genetic analysis methods to examine polymorphisms.
  • The findings indicated that the rare CC genotype significantly increased the risk of infection, with odds ratios showing a threefold risk compared to controls, highlighting a potential genetic factor in susceptibility to the disease.

Article Abstract

Toll-like receptors (TLRs), particularly the TLR2, take part in the elicitation of immune responses against . This study aimed to investigate the relationship between a specific polymorphism called rs3804099 in the gene and infection among Lebanese children. A case-control study encompassed 180 participants including 68 children with amebiasis and 112 matched controls. Blood samples were collected, and genomic DNA was extracted using the classical proteinase K digestion and phenol-chloroform extraction method. The variant rs3804099 was examined using the Amplification Refractory Mutation System Polymerase Chain Reaction. The accuracy of the genotyping was supported by sequencing 5% of samples. The rs3804099 polymorphism was identified in the studied population, and the observed genotypic distributions were consistent with equilibrium ( > 0.05). The frequency of the rare CC genotype was significantly higher in patients compared to the noninfected group ( < 0.01). In controls, the homozygous TT genotype was less frequent than the heterozygous CT genotype. The rare CC genotype was associated with a higher risk of amebiasis among children (odds ratios = 3.27, = 0.002). These findings provide evidence supporting the association between the rs3804099 SNP in the gene and infection among Lebanese children.

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Source
http://dx.doi.org/10.1089/jir.2024.0183DOI Listing

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