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Effects of enamel matrix genes on dental caries are moderated by fluoride exposures

机译:搪瓷基质基因对龋齿的影响可通过氟化物暴露来缓解

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摘要

Dental caries (tooth decay) is the most common chronic disease, worldwide, affecting most children and adults. Though dental caries is highly heritable, few caries-related genes have been discovered. We investigated whether 18 genetic variants in the group of nonamelogenin enamel matrix genes (AMBN, ENAM, TUFT1, and TFIP11) were associated with dental caries experience in 13 age- and race-stratified samples from six parent studies (N=3,600). Linear regression was used to model genetic associations and test gene-byfluoride interaction effects for two sources of fluoride: daily tooth brushing and home water fluoride concentration. Meta-analysis was used to combine results across five child and eight adult samples. We observed the statistically significant association of rs2337359 upstream of TUFT1 with dental caries experience via meta-analysis across adult samples (p<0.002) and the suggestive association for multiple variants in TFIP11 across child samples (p<0.05). Moreover, we discovered two genetic variants (rs2337359 upstream of TUFT1 and missense rs7439186 in AMBN) involved in gene-by-fluoride interactions. For each interaction, participants with the risk allele/genotype exhibited greater dental caries experience only if they were not exposed to the source of fluoride. Altogether, these results confirm that variation in enamel matrix genes contributes to individual differences in dental caries liability, and demonstrate that the effects of these genes may be moderated by protective fluoride exposures. In short, genes may exert greater influence on dental caries in unprotected environments, or equivalently, the protective effects of fluoride may obviate the effects of genetic risk alleles.
机译:龋齿(蛀牙)是世界范围内最常见的慢性疾病,影响大多数儿童和成人。尽管龋齿是高度可遗传的,但很少发现与龋齿相关的基因。我们调查了非釉原蛋白釉质基质基因(AMBN,ENAM,TUFT1和TFIP11)组中的18种遗传变异是否与来自六个父母研究的13个年龄和种族分层样本中的龋齿经历相关(N = 3,600)。线性回归被用来建立遗传联系的模型,并测试两种氟化物来源的基因-氟化物相互作用效应:日常刷牙和家庭用水中氟化物的浓度。荟萃分析用于合并五个儿童和八个成人样本的结果。我们通过成人样本之间的荟萃分析观察了TUFT1上游rs2337359与龋齿经验的统计显着相关性(p <0.002),而儿童样本中TFIP11的多个变体的暗示性相关性(p <0.05)。此外,我们发现了两个遗传变异(TUFT1上游的rs2337359和AMBN中的错义rs7439186)参与了基因与氟化物的相互作用。对于每次互动,只有等位基因/基因型风险参与者不暴露于氟化物源时,他们才会表现出更好的龋齿经历。总而言之,这些结果证实了釉质基质基因的变异导致了龋齿责任的个体差异,并证明了这些基因的作用可以通过保护性氟化物暴露来缓解。简而言之,基因可能在不受保护的环境中对龋齿产生更大的影响,或者等效地,氟化物的保护作用可能会消除遗传风险等位基因的影响。

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