Genetic Association between the Risk of Dental Caries and MTR Gene Polymorphism in Chinese Children.

IF 1.7 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Tohoku Journal of Experimental Medicine Pub Date : 2024-05-31 Epub Date: 2024-02-08 DOI:10.1620/tjem.2024.J011
Weilian Du, Lingzhen Liu, Fang Li, Shusen Xu
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引用次数: 0

Abstract

Early childhood caries (ECC) is common in children. Little is known about the genetic association of the methionine synthesis reductase (MTRR) gene rs1801394 and methionine synthetase (MTR) gene rs1805087 polymorphisms with ECC, which was examined in the Chinese Han population. Genotyping was performed using the buccal mucosa from 150 normal and 150 ECC children. For genotype and allele distribution comparison, Chi-square test and multiple logistic regression analysis were performed. The odd ratio (OR) and 95% confidence interval (CI) were calculated. MTR gene rs1805087 AG genotype distribution in the ECC group was clearly different from the control group (P = 0.029), and the ECC risk in cases with AG genotype was 0.525 times lower than those carrying AA genotype (95% CI = 0.292-0.942). Logistic regression analysis after adjustment for other clinical indicators determined that the MTR gene rs1805087 AG genotype was still strongly associated with susceptibility to ECC (OR = 0.499, 95% CI = 0.273-0.913, P = 0.024). Significant association was also seen for sugary food intakes (OR = 1.965, 95% CI = 1.162-3.321, P = 0.012), tooth brushing (OR = 0.569, 95% CI = 0.356-0.924, P = 0.023) and sex (OR = 0.562, 95% CI = 0.349-0.907, P = 0.018) with ECC risk. No notable genetic association was found between MTRR gene rs1801394 polymorphism and ECC risk. MTR gene rs1805087 polymorphism may aggrandize the susceptibility to ECC, and AA genotype appeared to be a dangerous element for the development of ECC.

中国儿童龋齿风险与 MTR 基因多态性之间的遗传关联
儿童早期龋齿(ECC)在儿童中很常见。关于蛋氨酸合成还原酶(MTRR)基因 rs1801394 和蛋氨酸合成酶(MTR)基因 rs1805087 多态性与 ECC 的遗传关联,人们知之甚少。基因分型使用了 150 名正常儿童和 150 名 ECC 儿童的口腔黏膜。在比较基因型和等位基因分布时,进行了卡方检验和多元逻辑回归分析。计算了奇异比(OR)和 95% 置信区间(CI)。ECC组的MTR基因rs1805087 AG基因型分布与对照组明显不同(P = 0.029),AG基因型病例的ECC风险比AA基因型病例低0.525倍(95% CI = 0.292-0.942)。调整其他临床指标后进行的逻辑回归分析表明,MTR基因rs1805087 AG基因型仍与ECC易感性密切相关(OR = 0.499,95% CI = 0.273-0.913,P = 0.024)。含糖食物摄入量(OR = 1.965,95% CI = 1.162-3.321,P = 0.012)、刷牙(OR = 0.569,95% CI = 0.356-0.924,P = 0.023)和性别(OR = 0.562,95% CI = 0.349-0.907,P = 0.018)与 ECC 风险也有显著关联。在 MTRR 基因 rs1801394 多态性与 ECC 风险之间未发现明显的遗传关联。MTR基因rs1805087多态性可能会增加ECC的易感性,而AA基因型似乎是ECC发病的危险因素。
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来源期刊
CiteScore
3.60
自引率
4.50%
发文量
171
审稿时长
1 months
期刊介绍: Our mission is to publish peer-reviewed papers in all branches of medical sciences including basic medicine, social medicine, clinical medicine, nursing sciences and disaster-prevention science, and to present new information of exceptional novelty, importance and interest to a broad readership of the TJEM. The TJEM is open to original articles in all branches of medical sciences from authors throughout the world. The TJEM also covers the fields of disaster-prevention science, including earthquake archeology. Case reports, which advance significantly our knowledge on medical sciences or practice, are also accepted. Review articles, Letters to the Editor, Commentary, and News and Views will also be considered. In particular, the TJEM welcomes full papers requiring prompt publication.
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