Cafiero Concetta, Grippaudo Cristina, Dell'Aquila Marco, Cimmino Pasquale, D'Addona Antonio, De Angelis Paolo, Ottaiano Maria Pia, Costagliola Domenico, Benincasa Giulio, Micera Alessandra, Santacroce Luigi, Palmirotta Raffaele
Pathology Unit, Fabrizio Spaziani Hospital, 03100 Frosinone, Italy.
Department of Head and Neck, Division of Oral Surgery and Implantology, Catholic University of the Sacred Heart, Fondazione Policlinico Gemelli IRCCS, 00168 Rome, Italy.
Biomolecules. 2022 Jun 15;12(6):833. doi: 10.3390/biom12060833.
Periodontitis is an inflammatory disease caused by microorganisms involving the supporting tissues of the teeth. Gene variants may influence both the composition of the biofilm in the oral cavity and the host response. The objective of the study was to investigate the potential correlations between the disease susceptibility, the presence and the quantity of periodontopathogenic oral bacterial composition and the VDR gene polymorphisms. Fifty (50) unrelated periodontal patients and forty-one (41) healthy controls were selected for genomic DNA extraction. DNA concentration was measured and analyzed. The periodontopathogenic bacterial species were identified and quantified using a Real Time PCR performed with species-specific primers and probes. Genotype distribution showed a different distribution between the groups for BsmI rs1544410 genotypes ( = 0.0001) with a prevalence of the G(b) allele in periodontal patients ( = 0.0003). Statistical significance was also found for VDR TaqI rs731236 ( ≤ 0.00001) with a prevalence of the T(T) allele in periodontal patients ( ≤ 0.00001). The average bacterial copy count for the periodontitis group was significantly higher than that of control group. Dividing patients into two groups based on high or low bacterial load, FokI rs2228570 T allele (f) was statistically more represented in patients with high bacterial load. The findings of the study suggest the involvement of the VDR gene BsmI and TaqI polymorphisms in periodontal disease, while FokI and BsmI may be involved in determining an increased presence of periodontopathogens.
牙周炎是一种由微生物引起的涉及牙齿支持组织的炎症性疾病。基因变异可能会影响口腔生物膜的组成以及宿主反应。本研究的目的是调查疾病易感性、牙周致病口腔细菌组成的存在及数量与维生素D受体(VDR)基因多态性之间的潜在相关性。选取了50名无亲属关系的牙周病患者和41名健康对照者进行基因组DNA提取。测量并分析DNA浓度。使用针对特定物种的引物和探针进行实时聚合酶链反应(Real Time PCR)来鉴定和定量牙周致病细菌种类。基因型分布显示,BsmI rs1544410基因型在两组之间分布不同(P = 0.0001),牙周病患者中G(b)等位基因的患病率较高(P = 0.0003)。对于VDR TaqI rs731236也发现了统计学意义(P ≤ 0.00001),牙周病患者中T(T)等位基因的患病率较高(P ≤ 0.00001)。牙周炎组的平均细菌拷贝数显著高于对照组。根据细菌载量高低将患者分为两组,FokI rs2228570 T等位基因(f)在细菌载量高的患者中在统计学上更具代表性。该研究结果表明VDR基因的BsmI和TaqI多态性与牙周疾病有关,而FokI和BsmI可能参与决定牙周病原体的增加存在。