Graduate Program in Oral Biology and Center of Excellence on Oral Microbiology and Immunology, Faculty of Dentistry, Chulalongkorn University, Wang-Mai, Pathumwan, Bangkok, Thailand.
Department of Microbiology and Center of Excellence on Oral Microbiology and Immunology, Faculty of Dentistry, Chulalongkorn University, Wang-Mai, Pathumwan, Bangkok, Thailand.
J Dent Res. 2023 Jun;102(6):626-635. doi: 10.1177/00220345231152802. Epub 2023 Mar 15.
Dental caries is the most common chronic disease in children that causes negative effects on their health, development, and well-being. Early preventive interventions are key to reduce early childhood caries prevalence. An efficient strategy is to provide risk-based targeted prevention; however, this requires an accurate caries risk predictor, which is still lacking for infants before caries onset. We aimed to develop a caries prediction model based on the salivary microbiome of caries-free 1-y-old children. Using a nested case-control design within a prospective cohort study, we selected 30 children based on their caries status at 1-y follow-up (at 2 y old): 10 children who remained caries-free, 10 who developed noncavitated caries, and 10 who developed cavitated caries. Saliva samples collected at baseline before caries onset were analyzed through 16S rRNA gene sequencing. The results of β diversity analysis showed a significant difference in salivary microbiome composition between children who remained caries-free and those who developed cavitated caries at 2 y old (analysis of similarities, Benjamini-Hochberg corrected, = 0.042). The relative abundance of , sp. HMT 215, , and in children who remained caries-free was significantly higher than in children who developed cavitated caries (Wilcoxon rank sum test, = 0.024, 0.040, 0.049, and 0.049, respectively). These taxa were also identified as biomarkers for children who remained caries-free (linear discriminant analysis effect size, linear discriminant analysis score = 3.69, 3.74, 3.53, and 3.46). A machine learning model based on these 4 species distinguished between 1-y-old children who did and did not develop cavitated caries at 2 y old, with an accuracy of 80%, sensitivity of 80%, and specificity of 80% (area under the curve, 0.8; 95% CI, 44.4 to 97.5). Our findings suggest that these salivary microbial biomarkers could assist in predicting future caries in caries-free 1-y-old children and, upon validation, are promising for development into an adjunctive tool for caries risk prediction for prevention and monitoring.
龋齿是儿童中最常见的慢性疾病,会对其健康、发育和幸福感产生负面影响。早期预防干预是降低儿童早期龋齿患病率的关键。一种有效的策略是提供基于风险的靶向预防;然而,这需要一个准确的龋齿风险预测器,而对于龋齿发病前的婴儿来说,这仍然是缺乏的。我们旨在基于无龋 1 岁儿童的唾液微生物组开发龋齿预测模型。使用前瞻性队列研究中的嵌套病例对照设计,我们根据 1 年随访时(2 岁时)的龋齿状况选择了 30 名儿童:10 名仍无龋的儿童、10 名发生非龋性龋齿的儿童和 10 名发生龋性龋齿的儿童。在龋齿发病前收集基线唾液样本,通过 16S rRNA 基因测序进行分析。β多样性分析结果显示,在 2 岁时仍无龋和发生龋性龋齿的儿童之间,唾液微生物组组成存在显著差异(相似性分析,Benjamini-Hochberg 校正, = 0.042)。在仍无龋的儿童中, 、 sp. HMT 215、 、 和 的相对丰度明显高于发生龋性龋齿的儿童(Wilcoxon 秩和检验, = 0.024、0.040、0.049 和 0.049)。这些分类群也被确定为仍无龋儿童的生物标志物(线性判别分析效应大小,线性判别分析评分 = 3.69、3.74、3.53 和 3.46)。基于这 4 个物种的机器学习模型能够区分在 2 岁时是否发生龋性龋齿的 1 岁儿童,准确率为 80%,敏感度为 80%,特异性为 80%(曲线下面积,0.8;95%CI,44.4 至 97.5)。我们的研究结果表明,这些唾液微生物生物标志物可用于预测无龋 1 岁儿童未来的龋齿,在验证后,它们有望成为龋齿风险预测的辅助工具,用于预防和监测。