Department of Stomatology, Universidade Federal do Paraná, Curitiba, PR, Brazil.
School of Dentistry, Guairaca College, Guarapuava, PR, Brazil.
Clin Oral Investig. 2020 Nov;24(11):3971-3980. doi: 10.1007/s00784-020-03263-y. Epub 2020 Mar 31.
The purpose of this cross-sectional study was to investigate whether polymorphisms in vitamin D receptor (VDR) genes increase the prevalence of dental caries, molar incisor hypomineralization (MIH), and hypomineralized primary second molars (HPSM).
A representative population-based sample of 731 schoolchildren, 8 years of age, was randomly selected in Curitiba, Paraná, Brazil. MIH, HPSM, and dental caries were clinically assessed by four calibrated examiners (kappa > 0.80) using European Academy of Pediatric Dentistry (2003) criteria, the modified Developmental Defects of Enamel (DDE) index, and the Decayed, Missing, or Filled Teeth (DMFT) index by the World Health Organization (2013), respectively. The VDR rs739837 and rs2228570 polymorphisms were genotyped using real-time polymerase chain reaction. Associations were analyzed by Poisson regression with robust variance (α = 0.05).
Schoolchildren with MIH presented a higher prevalence of dental caries (DMFT > 1, PR = 2.52, confidence interval = 1.60-3.97, p ≤ 0.001). No association was observed between MIH, HPSM, and dental caries, with rs739837 and rs2228570 polymorphisms. Individuals with the GT/GG genotype in rs739837 polymorphism presented a higher prevalence of MIH in molars and incisors than individuals TT (PR = 2.34, confidence interval = 1.08-5.07, p = 0.03).
Children with MIH presented a significant higher prevalence of dental caries than children without MIH. To carry at least one G allele in rs739837 was associated to higher prevalence of MIH in molars and incisors.
Our findings suggested that more severe cases with incisors affected by MIH could be associated with polymorphism in VDR gene.
本横断面研究旨在探讨维生素 D 受体(VDR)基因多态性是否会增加龋齿、磨牙切牙釉质发育不全(MIH)和低矿化乳第二磨牙(HPSM)的患病率。
在巴西巴拉那州库里蒂巴,随机选择了一个具有代表性的 731 名 8 岁学龄儿童的人群样本。使用欧洲儿童牙科学会(2003 年)标准、改良发育性牙釉质不全(DDE)指数和世界卫生组织(2013 年)的龋齿、缺失或补牙(DMFT)指数,由四位经过校准的检查者(kappa > 0.80)对 MIH、HPSM 和龋齿进行临床评估。VDR rs739837 和 rs2228570 多态性通过实时聚合酶链反应进行基因分型。采用泊松回归分析具有稳健方差(α = 0.05)。
患有 MIH 的儿童龋齿患病率更高(DMFT > 1,PR = 2.52,置信区间 1.60-3.97,p ≤ 0.001)。MIH、HPSM 和龋齿之间与 rs739837 和 rs2228570 多态性无关联。rs739837 多态性 GT/GG 基因型个体的磨牙和切牙 MIH 患病率高于 TT 个体(PR = 2.34,置信区间 1.08-5.07,p = 0.03)。
患有 MIH 的儿童龋齿患病率明显高于未患有 MIH 的儿童。rs739837 多态性中至少携带一个 G 等位基因与磨牙和切牙 MIH 患病率较高相关。
我们的研究结果表明,患有 MIH 的切牙病情较重的患者可能与 VDR 基因多态性有关。