Graduate Program in Dentistry, Federal University of Juiz de Fora, Governador Valadares, MG, Brazil.
International Center for Equity in Health, Postgraduate Program of Epidemiology, Federal University of Pelotas, Pelotas, Brazil.
J Dent Res. 2023 Apr;102(4):422-430. doi: 10.1177/00220345221138569. Epub 2023 Jan 7.
This study aims to investigate whether the trajectory of dental caries in the life course is associated with rs307355 () and rs35874116 () and if there is an epistatic association between rs307355 () and rs35874116 (). A representative sample of all 5,914 births from the 1982 Pelotas birth cohort was prospectively investigated, and the decayed, missing, and filled teeth (DMF-T) components were assessed at ages 15 ( = 888), 24 ( = 720), and 31 ( = 539) y. Group-based trajectory modeling was used to identify groups with similar trajectories of DMF-T components in the life course. Genetic material was collected, and rs307355 () and rs35874116 () were genotyped. Ethnicity was evaluated using ADMIXTURE. Generalized multifactor dimensionality reduction software was used to investigate epistatic interactions. Considering rs307355 () in the additive effect, the genotype TT was associated with the high decayed trajectory group (odds ratio [OR] = 4.52; 95% confidence interval [CI], 1.15-17.74) and the high missing trajectory group (OR = 3.35; 95% CI, 1.09-10.26). In the dominant effect, the genotype CT/TT was associated with the high decayed trajectory group (OR = 1.64; 95% CI, 1.14-2.35). Allele T was associated with an increased odds of 64% (OR = 1.64; 95% CI, 1.20-2.25) for the decayed component and 41% (OR = 1.41; 95% CI, 1.04-1.92) for the missing component. No associations were observed between rs307355 () and the filled component. rs35874116 () was not associated with DMF-T components. Positive epistatic interactions were observed involving rs307355 () and rs35874116 () with the decayed component (OR = 1.72; 95% CI, 1.04-2.84). Thus, rs307355 () genotypes and alleles seem positively associated with the trajectory of decayed and missing components in the life course. Epistatic interaction between rs307355 and rs35874116 may increase the decayed caries trajectory.
本研究旨在探讨生命历程中龋齿的轨迹是否与 rs307355()和 rs35874116()相关,以及 rs307355()和 rs35874116()之间是否存在上位性关联。前瞻性调查了来自 1982 年佩洛塔斯出生队列的所有 5914 名出生婴儿的代表性样本,并在 15 岁(n=888)、24 岁(n=720)和 31 岁(n=539)时评估了龋齿、缺失和填补牙齿(DMF-T)的成分。使用基于群组的轨迹建模来识别生命历程中 DMF-T 成分具有相似轨迹的群组。收集遗传物质,并对 rs307355()和 rs35874116()进行基因分型。使用 ADMIXTURE 评估种族。使用广义多因素维度缩减软件研究上位性相互作用。考虑到 rs307355()的加性效应,基因型 TT 与高龋齿轨迹组(比值比[OR] = 4.52;95%置信区间[CI],1.15-17.74)和高缺失轨迹组(OR = 3.35;95%CI,1.09-10.26)相关。在显性效应中,基因型 CT/TT 与高龋齿轨迹组相关(OR = 1.64;95%CI,1.14-2.35)。等位基因 T 与龋齿成分的 64%(OR = 1.64;95%CI,1.20-2.25)和缺失成分的 41%(OR = 1.41;95%CI,1.04-1.92)的比值增加相关。rs307355()与 DMF-T 成分无关。rs35874116()与 DMF-T 成分无关。rs307355()和 rs35874116()与龋齿成分之间存在阳性上位性相互作用(OR = 1.72;95%CI,1.04-2.84)。因此,rs307355()基因型和等位基因似乎与生命历程中龋齿和缺失成分的轨迹呈正相关。rs307355 与 rs35874116 之间的上位性相互作用可能会增加龋齿的轨迹。