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重新定义龋齿的表型。

Redefining the Phenotype of Dental Caries.

机构信息

University of Pittsburgh School of Dental Medicine, Pittsburgh, PA, USA.

出版信息

Caries Res. 2018;52(4):263-271. doi: 10.1159/000481414. Epub 2018 Jan 25.

DOI:10.1159/000481414
PMID:29393149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6013308/
Abstract

Dental caries is a multifactorial infectious disease and a major public health problem estimated to affect 60-90% of school children as well as a vast number of adults. The aim of this work was to define patterns of progression of the disease based on longitudinal data in contrast to using a cross-sectional assessment. dmft/DMFT scores were collected at ages 5, 12, 14, 16, 17, and 18 from 876 individuals. We tested our newly defined phenotypes for association with genetic variants in genes shown to be associated with caries. We generated genotyping data using Taqman chemistry in markers of genes involved in processes such as enamel formation and salivary contributions. Kallikrein 4 (KLK4) was found to show a significant association with the created phenotypes (p = 0.0008 in a recessive model for low caries experience in the primary dentition vs. high caries experience in the primary dentition, and p = 0.0004 in a recessive model for caries free primary dentition vs. high caries experience in the primary dentition).

摘要

龋齿是一种多因素的传染病,也是一个主要的公共卫生问题,据估计,它会影响 60-90%的学龄儿童以及大量成年人。这项工作的目的是根据纵向数据来定义疾病的进展模式,而不是使用横断面评估。从 876 个人中收集了 dmft/DMFT 评分,这些人在 5 岁、12 岁、14 岁、16 岁、17 岁和 18 岁时进行了测量。我们测试了我们新定义的表型与已证明与龋齿相关的基因中的遗传变异之间的关联。我们使用 Taqman 化学方法在参与牙釉质形成和唾液贡献等过程的基因的标记物中生成了基因分型数据。Kallikrein 4 (KLK4) 被发现与创建的表型显著相关(在原发性牙齿中低龋齿经历的隐性模型中,与高龋齿经历相比,p = 0.0008,在原发性牙齿中无龋齿经历的隐性模型中,与高龋齿经历相比,p = 0.0004)。

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本文引用的文献

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Meta-analysis of teeth from European populations before and after the 18th century reveals a shift towards increased prevalence of caries and tooth loss.对18世纪前后欧洲人群牙齿的荟萃分析显示,龋齿和牙齿脱落的患病率呈上升趋势。
Arch Oral Biol. 2017 Jan;73:7-15. doi: 10.1016/j.archoralbio.2016.08.018. Epub 2016 Aug 20.
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Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries.水通道蛋白5与氟化物相互作用并可能预防龋齿。
PLoS One. 2015 Dec 2;10(12):e0143068. doi: 10.1371/journal.pone.0143068. eCollection 2015.
3
Gene-environment Interactions in the Etiology of Dental Caries.
[某些基因]、[某些基因]和[某些基因]的多态性使埃及成年人易患龋齿:一项横断面研究。 (注:原文中未明确写出具体是哪些基因,这里用[某些基因]代替)
Saudi Dent J. 2024 Jun;36(6):915-919. doi: 10.1016/j.sdentj.2024.03.014. Epub 2024 Mar 20.
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Association of Dental Caries in Primary Teeth With HLA Class II Gene Among Syrian Children.叙利亚儿童乳牙龋齿与人类白细胞抗原II类基因的关联
Cureus. 2024 Jan 27;16(1):e53081. doi: 10.7759/cureus.53081. eCollection 2024 Jan.
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Association between polymorphisms of immune response genes and early childhood caries - systematic review, gene-based, gene cluster, and meta-analysis.免疫反应基因多态性与幼儿龋齿之间的关联——系统评价、基于基因的研究、基因簇分析和荟萃分析
J Genet Eng Biotechnol. 2023 Nov 16;21(1):124. doi: 10.1186/s43141-023-00566-x.
6
Dental Caries Risk Assessment in Children 5 Years Old and under via Machine Learning.通过机器学习对5岁及以下儿童进行龋齿风险评估。
Dent J (Basel). 2022 Sep 1;10(9):164. doi: 10.3390/dj10090164.
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Current State and Challenges of the Global Outcomes of Dental Caries Research in the Meta-Omics Era.元组学时代全球龋齿研究结局的现状与挑战
Front Cell Infect Microbiol. 2022 Jun 17;12:887907. doi: 10.3389/fcimb.2022.887907. eCollection 2022.
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Clin Oral Investig. 2020 Nov;24(11):3723-3738. doi: 10.1007/s00784-019-03146-x. Epub 2020 Sep 18.
基因-环境交互作用在龋齿发病机制中的作用。
J Dent Res. 2016 Jan;95(1):74-9. doi: 10.1177/0022034515605281. Epub 2015 Sep 16.
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Eur Arch Paediatr Dent. 2014 Jun;15(3):211-6. doi: 10.1007/s40368-013-0096-6. Epub 2013 Nov 8.
10
Genetic mapping of high caries experience on human chromosome 13.人类染色体 13 上高龋齿体验的遗传定位。
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