Marian Diana, Rusu Darian, Stratul Stefan-Ioan, Calniceanu Horia, Sculean Anton, Anghel Andrei
Oral Health Prev Dent. 2019;17(2):157-165. doi: 10.3290/j.ohpd.a39738.
Recent data indicate that gene polymorphisms, e.g. those of vitamin D-receptor (VDR), are associated with an increased susceptibility to chronic periodontitis (CP). This study investigated whether VDR gene polymorphism is associated with chronic periodontitis in a population in Western Romania, by determining the prevalence of the BsmI (rs1544410), ApaI (rs7975232), TaqI (rs731236) and FokI (rs2228570) genotypes and comparing the CP group with a periodontally healthy group.
This case-control study included 53 patients with CP and 47 healthy patients. VDR polymorphisms were genotyped using real-time polymerase chain reaction (PCR). The associations between VDR polymorphisms and CP were determined using logistic regression models, adjusted for patient age and serum level of Vitamin D.
We found a statistically significant association between the single nucleotide polymorphism (SNP) rs2228570 (FokI) and CP. Compared with subjects having the Thymine-Thymine (TT) genotype, those with the Cytosine-Cytosine (CC) variant were 19 times more likely to have the disease (adjusted odd ratio [OR]: 19.58; 95% confidence interval [CI]: 2.67 - 198.92) and with the Thymine-Cytosine (TC) variant, 8 times more likely (adjusted OR: 7.86; 95% CI: 1.29 - 61.56). Also, for the SNP rs1544410 (BsmI), compared with the Adenine-Adenine (AA) genotype, the Adenine-Guanine (AG) variant had an increased risk of periodontal disease (crude OR: 3.76; 95% CI: 1.15 - 13.80).
This case-control study of a Western Romanian population shows an association between vitamin D receptor (VDR) polymorphisms (FokI and BsmI) and CP susceptibility.
近期数据表明,基因多态性,如维生素D受体(VDR)的多态性,与慢性牙周炎(CP)易感性增加有关。本研究通过测定BsmI(rs1544410)、ApaI(rs7975232)、TaqI(rs731236)和FokI(rs2228570)基因型的患病率,并将CP组与牙周健康组进行比较,调查罗马尼亚西部人群中VDR基因多态性是否与慢性牙周炎有关。
本病例对照研究包括53例CP患者和47例健康患者。使用实时聚合酶链反应(PCR)对VDR多态性进行基因分型。采用逻辑回归模型确定VDR多态性与CP之间的关联,并对患者年龄和血清维生素D水平进行校正。
我们发现单核苷酸多态性(SNP)rs2228570(FokI)与CP之间存在统计学显著关联。与胸腺嘧啶-胸腺嘧啶(TT)基因型的受试者相比,胞嘧啶-胞嘧啶(CC)变异型受试者患该病的可能性高19倍(校正比值比[OR]:19.58;95%置信区间[CI]:2.67 - 198.92),与胸腺嘧啶-胞嘧啶(TC)变异型相比,高8倍(校正OR:7.86;95%CI:1.29 - 61.56)。此外,对于SNP rs1544410(BsmI),与腺嘌呤-腺嘌呤(AA)基因型相比,腺嘌呤-鸟嘌呤(AG)变异型患牙周病的风险增加(粗OR:3.76;95%CI:1.15 - 13.80)。
这项对罗马尼亚西部人群的病例对照研究表明,维生素D受体(VDR)多态性(FokI和BsmI)与CP易感性之间存在关联。