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基质金属蛋白酶-1基因多态性与下颌后缩的关系。

Relationship between matrilin-1 gene polymorphisms and mandibular retrognathism.

作者信息

Balkhande Pranita B, Lakkakula Bhaskar V K S, Chitharanjan Arun B

机构信息

Department of Orthodontics and Dentofacial Orthopaedics, Sri Ramachandra University, Porur, Chennai, India.

Sickle Cell Institute, Chhattisgarh, Raipur, India.

出版信息

Am J Orthod Dentofacial Orthop. 2018 Feb;153(2):255-261.e1. doi: 10.1016/j.ajodo.2017.06.023.

Abstract

INTRODUCTION

Mandibular retrognathism is a type of malocclusion that refers to an abnormal posterior position of the mandible as a result of a developmental abnormality. From the literature, it is evident that the mandibular growth pattern is determined by the intramembranous ossification of the mandibular body and endochondral ossification of the condyle. Matrilin-1 is a cartilage extracellular matrix protein, and matrilin-1 gene (MATN1) polymorphisms have been found to be involved in dental malocclusions of humans. In this study, we aimed to examine the association between MATN1 polymorphisms and the risk of mandibular retrognathism, in a case-control study with a South Indian population.

METHODS

Eighty-one patients with mandibular retrognathism (SNB, <78°) and 71 controls having an orthognathic mandible (SNB, 80° ± 2°) were recruited. In both the patient and control groups, subjects with an orthognathic maxilla (SNA, 82° ± 2°) were included. Three single nucleotide polymorphisms of the MATN1 gene (rs1149048, rs1149042, and rs1065755) were genotyped using polymerase chain reaction-restriction fragment length polymorphism. The statistical association analysis was performed using the chi-square test. Pair-wise linkage disequilibrium was computed, and haplotypes were compared between subjects and controls. Nonparametric tests were used to compare cephalometric measurements between groups.

RESULTS

No polymorphic site deviated from Hardy-Weinberg equilibrium in the controls. The rs1149042 genotypes and alleles were found to be associated with reduced risk of mandibular retrognathism. Furthermore, rs1149042 genotypes were associated with mandibular measurements (SNB and ANB). There was no strong and consistent linkage disequilibrium linkage disequilibrium across two different single nucleotide polymorphisms and haplotypes were not associated with mandibular retrognathism.

CONCLUSIONS

The results of our study suggest an association between the MATN1 gene polymorphisms and mandibular retrognathism.

摘要

引言

下颌后缩是一种错牙合畸形,指由于发育异常导致下颌骨处于异常的后位。从文献中可知,下颌骨的生长模式由下颌体的膜内成骨和髁突的软骨内成骨决定。基质金属蛋白酶-1是一种软骨细胞外基质蛋白,已发现基质金属蛋白酶-1基因(MATN1)多态性与人类牙齿错牙合畸形有关。在本研究中,我们旨在通过一项针对南印度人群的病例对照研究,探讨MATN1多态性与下颌后缩风险之间的关联。

方法

招募了81名下颌后缩患者(SNB,<78°)和71名具有正常下颌骨的对照者(SNB,80°±2°)。患者组和对照组均纳入上颌骨正常的受试者(SNA,82°±2°)。使用聚合酶链反应-限制性片段长度多态性对MATN1基因的三个单核苷酸多态性(rs1149048、rs1149042和rs1065755)进行基因分型。采用卡方检验进行统计关联分析。计算成对连锁不平衡,并比较受试者与对照者之间的单倍型。使用非参数检验比较组间的头影测量值。

结果

对照组中无多态性位点偏离哈迪-温伯格平衡。发现rs1149042基因型和等位基因与下颌后缩风险降低有关。此外,rs1149042基因型与下颌测量值(SNB和ANB)有关。在两个不同的单核苷酸多态性之间没有强且一致的连锁不平衡,单倍型与下颌后缩无关。

结论

我们的研究结果表明MATN1基因多态性与下颌后缩之间存在关联。

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