Department of Hygiene and Epidemiology, Pomeranian Medical University in Szczecin, Powstańców Wlkp. 72, 70-111 Szczecin, Poland.
Department of General Pharmacology and Pharmacoeconomics, Pomeranian Medical University in Szczecin, Żołnierska 48, 71-210 Szczecin, Poland.
Int J Mol Sci. 2024 Jun 26;25(13):6985. doi: 10.3390/ijms25136985.
The aim of the present study was to analyze the association of the (Toll-like receptor 2 gene) 2258G>A (rs5743708), (Toll-like receptor 4 gene) 896A>G (rs4986790), and 1196C>T (rs4986791) polymorphisms with dental caries in Polish children. The participants, 261 15-year-old children, were divided into two groups: 82 cases (i.e., children with DMFT (Decayed, Missing, and Filled Teeth) index >5, having either moderate or high caries experience, assigned as the "higher" caries experience group) and 179 controls (i.e., children with DMFT ≤ 5, having either low or very low caries experience, assigned as the "lower" caries experience group). Genomic DNA was isolated from buccal swabs, and genotyping was determined by means of real-time PCR (polymerase chain reaction). There were no significant differences in the genotype or allele distributions in all tested SNPs (single nucleotide polymorphisms) between children with "higher" caries experience and those with "lower" caries experience. haplotype frequencies did not differ significantly between cases and controls. In an additional analysis with another case definition applied (subjects with DMFT ≥ 1 were assigned as "cases", whereas children with DMFT = 0 were assigned as "controls"), no significant differences in the and genotype, allele frequencies, and haplotype frequencies were found between the case and the control groups. The results of the present study broaden our knowledge on the potential genetic factors that might affect caries risk and suggest that rs5743708 and rs4986790 and rs4986791 SNPs are not associated with dental caries susceptibility in Polish children.
本研究旨在分析波兰儿童中 (Toll 样受体 2 基因)2258G>A(rs5743708)、 (Toll 样受体 4 基因)896A>G(rs4986790)和 1196C>T(rs4986791)多态性与龋齿的关系。参与者为 261 名 15 岁儿童,分为两组:82 例(DMFT(龋失补牙数)指数>5,具有中等到高度龋齿经验,分为“较高”龋齿经验组)和 179 例对照(DMFT≤5,具有低到非常低的龋齿经验,分为“较低”龋齿经验组)。从颊拭子中提取基因组 DNA,采用实时 PCR(聚合酶链反应)进行基因分型。在所有测试的 SNP(单核苷酸多态性)中,“较高”龋齿经验儿童与“较低”龋齿经验儿童之间的基因型或等位基因分布无显著差异。病例组和对照组之间的 haplotype 频率也无显著差异。在应用另一种病例定义的额外分析中(DMFT≥1 的受试者被分配为“病例”,而 DMFT=0 的儿童被分配为“对照”),病例组和对照组之间的 和 基因型、等位基因频率和 haplotype 频率无显著差异。本研究的结果拓宽了我们对可能影响龋齿风险的潜在遗传因素的认识,并表明 rs5743708 和 rs4986790 和 rs4986791 SNPs 与波兰儿童的龋齿易感性无关。