Relationship Between Gene Polymorphisms of the Renin-Angiotensin System and Dental Caries Experience

Sergey N. Levitsky, Natalia A. Bebyakova, Nadezhda G. Davydova, Aleksandra S. Galieva
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Abstract

When it comes to studying periodontal diseases and their correlation with general physical pathology, the relationship between the state of oral organs and tissues and the haemodynamic system is of interest; however, research is often conducted without taking into account molecular genetic determinants. The purpose of this article was to determine the relationship of the T704C and C521C polymorphisms of the angiotensinogen (AGT) gene and A1166C polymorphism of the angiotensin II receptor type 1 (AGT2R1) gene with dental caries experience in young people living in the European North of Russa. Materials and methods. The research included 57 healthy male and female subjects (mean age 18.2 years; confidence interval 17.9–19.4) permanently residing in the Arkhangelsk Region. The polymorphisms under study were genotyped by means of pyrosequencing; their allele and genotype frequencies were determined. Angiotensin II level in blood plasma was measured using enzyme-linked immunosorbent assay. Decay-missing-filled (DMF) index and forms of caries in subjects with and without mutant alleles for each gene variant were determined. Results. Young individuals with mutant AGT and AGT2R1 gene alleles showed high DMF index; however, a statistically significant increase in DMF index was observed only in the case of the T704C polymorphism. Angiotensin II levels in young subjects did not differ statistically significantly by sex; however, a tendency was observed towards increased angiotensin II level in the presence of mutant alleles of all the genes under study in the genotype. Among the carriers of the mutant C allele of the T704C polymorphism of the AGT gene, subjects with the decompensated form of caries prevailed, while carriers of the mutant T allele of the C521T polymorphism of the AGT gene showed higher frequency of the subcompensated form of caries. Carriers of the mutant C allele of the A1166C polymorphism of the AGT2R1 gene demonstrated increased frequency of the compensated form of caries with a slight decrease in the frequency of the subcompensated and decompensated forms.
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肾素-血管紧张素系统基因多态性与龋齿经历之间的关系
在研究牙周疾病及其与一般生理病理的相关性时,口腔器官和组织的状态与血液动力系统之间的关系很受关注;然而,研究往往没有考虑到分子遗传决定因素。本文旨在确定血管紧张素原(AGT)基因的 T704C 和 C521C 多态性以及血管紧张素 II 受体 1 型(AGT2R1)基因的 A1166C 多态性与居住在俄罗斯欧洲北部的年轻人龋齿经历的关系。材料与方法研究对象包括 57 名常住阿尔汉格尔斯克州的健康男性和女性受试者(平均年龄 18.2 岁;可信区间 17.9-19.4)。研究中的多态性通过热测序法进行了基因分型,并确定了其等位基因和基因型频率。血浆中的血管紧张素 II 水平是通过酶联免疫吸附法测定的。测定了每种基因变异的突变等位基因和非突变等位基因受试者的龋齿缺失指数(DMF)和龋齿形式。结果显示AGT和AGT2R1基因等位基因突变的年轻人显示出较高的DMF指数;然而,只有在T704C多态性的情况下,DMF指数才会出现统计学意义上的显著增加。年轻受试者的血管紧张素 II 水平在统计学上没有明显的性别差异;但是,如果基因型中存在所有研究基因的突变等位基因,则血管紧张素 II 水平有升高的趋势。在 AGT 基因 T704C 多态性突变等位基因 C 的携带者中,患有失代偿型龋齿的受试者居多,而 AGT 基因 C521T 多态性突变等位基因 T 的携带者患有亚代偿型龋齿的频率较高。AGT2R1 基因 A1166C 多态性突变等位基因 C 的携带者患代偿型龋齿的频率增加,而患亚代偿型和失代偿型龋齿的频率略有下降。
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