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基质金属蛋白酶基因变异与捷克儿童龋齿的关系。

Matrix metalloproteinases gene variants and dental caries in Czech children.

机构信息

Clinic of Stomatology, Institution Shared with St. Anne's University Hospital, Faculty of Medicine, Masaryk University, Pekarska 53, 656 91, Brno, Czech Republic.

Department of Pathophysiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.

出版信息

BMC Oral Health. 2020 May 12;20(1):138. doi: 10.1186/s12903-020-01130-6.

Abstract

BACKGROUND

Matrix metalloproteinases (MMPs) play an important role in tooth formation and the mineralization of dental tissue. The aim of the study was to analyse Czech children with primary/permanent dentition polymorphisms in those genes encoding MMP2, MMP3, MMP9, MMP13, MMP16, and MMP20, which had been previously associated with dental caries in other populations.

METHODS

In total, 782 Czech children were included in this case-control study. DNA samples were taken from 474 subjects with dental caries (with decayed/missing/filled teeth, DMFT ≥ 1) and 155 caries free children (DMFT = 0) aged 13-15 years, as well as 101 preschool children with early childhood caries (ECC, dmft ≥ 1) and 52 caries free children (dmft = 0), were analyzed for nine MMPs single nucleotide polymorphisms (SNPs) using real time polymerase chain reaction TaqMan assays.

RESULTS

There were no significant differences in the allele and/or genotype frequencies of all the studied MMPs SNPs among children with dental caries in primary/permanent dentition and the healthy controls (P > 0.05). In addition, similar allele or genotype frequencies of the studied MMPs SNPs were found in children with severe dental caries in their permanent teeth (children with DMFT ≥ 6) and the healthy controls (DMFT = 0, P > 0.05).

CONCLUSIONS

This study demonstrated the lack of association between the selected SNPs in candidate genes of MMPs and the susceptibility to or severity of dental caries in both primary and permanent dentitions in Czech children.

摘要

背景

基质金属蛋白酶(MMPs)在牙齿形成和牙组织矿化中发挥重要作用。本研究旨在分析捷克儿童在编码 MMP2、MMP3、MMP9、MMP13、MMP16 和 MMP20 的基因中的多态性,这些基因与其他人群的龋齿有关。

方法

本病例对照研究共纳入 782 名捷克儿童。从 474 名患有龋齿的儿童(有龋齿/缺失/补牙,DMFT≥1)和 155 名无龋齿的儿童(DMFT=0)、101 名患有早期儿童龋(ECC,dmft≥1)的学龄前儿童和 52 名无龋齿的儿童(dmft=0)中抽取 DNA 样本,采用实时聚合酶链反应 TaqMan 分析 9 种 MMPs 单核苷酸多态性(SNP)。

结果

在乳牙和恒牙有龋齿的儿童与健康对照组之间,所有研究 MMPs SNP 的等位基因和/或基因型频率均无显著差异(P>0.05)。此外,在恒牙严重龋齿(DMFT≥6)的儿童和健康对照组(DMFT=0)中,研究 MMPs SNP 的等位基因或基因型频率相似(P>0.05)。

结论

本研究表明,候选基因 MMPs 中选定 SNP 与捷克儿童乳牙和恒牙龋齿易感性或严重程度之间不存在关联。

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