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编码Ⅱ型胶原α1链的基因与下颌运动的关系。

Involvement of the gene encoding the collagen type II alpha 1 chain in mandibular mobility.

作者信息

Cavalcante-Leão Bianca, Brancher João Armando, Bertoli Fernanda, Meger Michelle Nascimento, Batista Luisa Helena, Vilalba Thais, de Menezes-Oliveira Maria Angélica Hueb, Baratto-Filho Flares, Kirschneck Christian, Feltrin-Souza Juliana, Küchler Erika Calvano

机构信息

School of Dentistry, Tuiuti University of Paraná, Curitiba, Paraná, Brazil.

Postgraduate Program in Cell and Molecular Biology, Federal University of Paraná, Curitiba, PR, Brazil.

出版信息

BMC Oral Health. 2025 Jun 25;25(1):958. doi: 10.1186/s12903-025-06245-2.

Abstract

BACKGROUND

There are no studies investigating the role of COL2A1 genes for mandibular mobility. The aim of this study was investigate the association between mandible mobility with single nucleotide polymorphisms (SNPs) in gene encoding collagen type II alpha 1 chain (COL2A1).

METHODS

Adolescents age from 10 to 14 years old without restrictions in mandibular movement were evaluated. The mandibular mobility was recorded using rule. Genomic DNA was obtained from saliva and the SNPs in COL2A1 gene (rs1793953 and rs2276454) were genotyped by real time polymerase chain reactions. One-way ANOVA with Tukey's post-test was used to compare the mean values of the mandibular mobility among genotypes in the co-dominant model. A linear regression analysis was also performed.

RESULTS

99 adolescents were included (53 boys and 46 girls). Gender and age were not associated with mandibular movements. For the rs1793953, unassisted opening, assisted opening and contralateral movements were statistically different among genotypes. The rs2276454 was associated with larger protrusive movements, in patients carrying TT genotype presented higher protrusion mean values than CT and TT individuals (p = 0.0046).

CONCLUSIONS

Our findings suggest that genes may play an essential role for the normal variation in mandibular movement and SNPs rs1793953 and rs2276454 in COL2A1 may explain mandibular mobility variations.

摘要

背景

尚无研究调查COL2A1基因在颌骨活动度方面的作用。本研究的目的是调查编码II型胶原α1链(COL2A1)的基因中的单核苷酸多态性(SNP)与下颌骨活动度之间的关联。

方法

对10至14岁下颌运动无限制的青少年进行评估。使用量表记录下颌活动度。从唾液中获取基因组DNA,并通过实时聚合酶链反应对COL2A1基因中的SNP(rs1793953和rs2276454)进行基因分型。在共显性模型中,采用单因素方差分析和Tukey事后检验比较各基因型下颌活动度的平均值。还进行了线性回归分析。

结果

纳入99名青少年(53名男孩和46名女孩)。性别和年龄与下颌运动无关。对于rs1793953,各基因型在自主开口、辅助开口和对侧运动方面存在统计学差异。rs2276454与更大的前伸运动有关,携带TT基因型的患者前伸平均值高于CT和TT个体(p = 0.0046)。

结论

我们的研究结果表明,基因可能在颌骨运动正常变异中起重要作用,COL2A1基因中的SNP rs1793953和rs2276454可能解释下颌活动度的变异。

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