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中国汉族人群中EDAR基因多态性与非综合征型牙发育不全的关联

Association between EDAR Polymorphisms and Non-Syndromic Tooth Agenesis in the Chinese Han Population.

作者信息

Chen Yi Ting, Liu Hao Chen, Han Dong, Liu Yang, Feng Hai Lan

出版信息

Chin J Dent Res. 2017;20(3):153-159. doi: 10.3290/j.cjdr.a38770.

Abstract

OBJECTIVE

To explore the relationship between single nuclear polymorphisms (SNPs) in ectodysplasin A receptor (EDAR) and EDAR-associated death domain (EDARADD) genes and non-syndromic tooth agenesis.

METHODS

Ten putative SNPs in EDAR and EDARADD were selected, and a case-control study was conducted in 112 subjects with non-syndromic tooth agenesis and 112 normal control subjects. DNA was obtained from peripheral blood samples. Genotyping was performed by Sanger sequencing.

RESULTS

Three SNPs (rs3749098, rs3749099, and rs10432616) in EDAR exhibited significant differences in the alleles and/or genotype frequencies between the case group (individuals with non-syndromic tooth agenesis) and control group (normal individuals). The T allele was identified in the SNP rs3749098 in 99.1% of the case group and in 96.0% of the control group (P = 0.0326). Regarding the SNP rs3749099, the C allele was identified in 99.1% of the case group and in 96.0% of the control group (P = 0.0326). Regarding the SNP rs10432616, the C allele was identified in 97.8% of the case group and in 100.0% of the control group (P = 0.0245).

CONCLUSION

Our results suggested that SNPs in EDAR could be a pathogenic factor for non-syndromic tooth agenesis. Furthermore, EDAR can be regarded as a marker gene for the risk of tooth agenesis.

摘要

目的

探讨外胚层发育不良蛋白A受体(EDAR)和EDAR相关死亡结构域(EDARADD)基因中的单核苷酸多态性(SNP)与非综合征性牙齿缺失之间的关系。

方法

选择EDAR和EDARADD中的10个假定SNP,对112例非综合征性牙齿缺失患者和112例正常对照者进行病例对照研究。从外周血样本中获取DNA。采用桑格测序法进行基因分型。

结果

EDAR中的3个SNP(rs3749098、rs3749099和rs10432616)在病例组(非综合征性牙齿缺失个体)和对照组(正常个体)之间的等位基因和/或基因型频率存在显著差异。在rs3749098 SNP中,病例组99.1%的个体检测到T等位基因,对照组96.0%的个体检测到T等位基因(P = 0.0326)。对于rs3749099 SNP,病例组99.1%的个体检测到C等位基因,对照组96.0%的个体检测到C等位基因(P = 0.0326)。对于rs10432616 SNP,病例组97.8%的个体检测到C等位基因,对照组100.0%的个体检测到C等位基因(P = 0.0245)。

结论

我们的结果表明,EDAR中的SNP可能是非综合征性牙齿缺失的致病因素。此外,EDAR可被视为牙齿缺失风险的标记基因。

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