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Relationship of the rs10850110 and rs11611277 polymorphisms of the MYO1H gene with non-syndromic mandibular prognathism in the Iranian population

机译:伊朗人口对非综合颌骨颌骨预后的rs10850110和rs11611277多态性的关系

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Background. The myosin 1H (MYO1H) gene, located on chromosome 12, encodes the unconventional MYO1H protein, which is involved in the intracellular movement and morphology of?chondrocytes, and plays a?vital role in the prognathism or retrognathism of?the mandible. Objectives. The objective of?this study was to assess the relationship between the polymorphisms of?the MYO1H gene and mandibular prognathism in the Iranian population. Material and methods. The current project evaluated 64 patients with mandibular prognathism requiring orthognathic surgery and 60 controls with skeletal class I occlusion. Genome amplification was performed using specific primer pairs to assess the rs10850110 and rs11611277 polymorphisms of?the MYO1H gene through the polymerase chain reaction (PCR). The restriction fragment length polymorphism (RFLP) technique was used to detect single-nucleotide polymorphisms. The data was analyzed using the χ 2 test. Results. The patient and control groups were not significantly different in terms of? age or gender (p??0.05). In all, 3.1% of?patients and 6.7% of?controls had the rs10850110 polymorphism (p?=?0.680), and 1.6% of?patients and 5% of?controls had the rs11611277 polymorphism (p?=?0.602). Conclusions. No significant correlation was noted between the rs10850110 and rs11611277 polymorphisms of?the MYO1H gene and mandibular prognathism in the Iranian population. However, the lower frequency of?these polymorphisms in the patient group suggests a?possible association with mandibular retrognathism, which needs to be investigated with a?larger sample size.
机译:背景。位于染色体12上的肌球蛋白1H(MyO1H)基因编码非传统的MyO1H蛋白,其参与细胞内运动和形态的蛋白质?软骨细胞,并在预后或回肠中发挥作用?下颌骨。目标。本研究的目的是评估伊朗人口中肌肉1H基因的多态性与颌骨颌骨预后之间的关系。材料与方法。目前的项目评估了64例颌骨预后患者,需要正畸手术和60例用骨骼级闭塞的对照。使用特异性引物对进行基因组扩增,以评估RS10850110和RS11611277通过聚合酶链式反应(PCR)的myO1H基因的多态性。限制片段长度多态性(RFLP)技术用于检测单核苷酸多态性。使用χ2检验分析数据。结果。患者和对照组在什么方面没有显着差异年龄或性别(p?> 0.05)。总而言之,3.1%的患者和6.7%的控制有Rs10850110多态性(p?= 0.680),1.6%?患者和5%的患者有1R11611277多态性(p?= 0.602)。结论。 RS10850110与RS11611277多态性没有显着相关性?伊朗人群中的myO1H基因和下颌预后性。然而,较低的频率?患者组中的这些多态性表明了与下颌再冻死的可能性,这需要用较大的样本量来研究。

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