Genetic variants and anterior cruciate ligament rupture – elastin proteins gene and fibromodulin gene polymorphisms

IF 0.7 Q4 SPORT SCIENCES
E. Lulinska, J. Żelazny, Agnieszka Lulińska, Elzbieta Grzywacz, Aleksandra Stroinska-Pluta, M. Sawczuk
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引用次数: 0

Abstract

Introduction: Anterior cruciate ligament (ACL) injuries are among the most common ligament injuries of the knee and often require reconstruction. The etiology of the molecular mechanisms of rupture of the anterior cruciate ligament (ACL) is poorly understood, and many external and internal factors have been associated with it, including genetics. This study aimed to investigate the association of sequence variants in the ELN and FMOD candidate genes with ACL ruptures based on the essential biological functions of these two proteoglycan-encoding genes in maintaining the structural integrity of tissues and regulating fibrillogenesis. Material and Methods: The partici-pants consisted of 229 (164 male and 65 female) individuals with a surgically diagnosed ACL rup-ture (ACLR) who qualified for ligament reconstruction and 192 (107 male and 85 female) healthy participants with no history of ACL injury (CON group). All 229 participants in the ACLR group sustained injuries through non-contact mechanisms. The chi-square tests were used for association analysis of ELN rs2071307 and FMOD rs7543148 between the anterior cruciate ligament rupture (ACLR) group and the control (CON) group. Results: It follows from the study that the tested group of athletes shows a statistically significantly more frequent AA genotype in the ELN rs2071307 gene polymorphism than the control group. However, looking at gender, one can observe that these are significantly more frequent. In the polymorphism of the FMOD rs7543148 gene, a significantly rarer TT genotype was observed in the study group compared to the control group and, similarly to the previous polymorphism, the TT genotype was significantly less frequent in the group of males com-pared to the control group. Conclusions: Genetic research in sports, especially concerning injuries connected to characteristic polymorphic variants of selected genes, is justified, particularly as regards gender-homogenous groups.
遗传变异和前交叉韧带断裂-弹性蛋白基因和纤维调节蛋白基因多态性
前言:前交叉韧带(ACL)损伤是膝关节最常见的韧带损伤之一,通常需要重建。前交叉韧带(ACL)断裂的分子机制的病因学尚不清楚,许多外部和内部因素与之相关,包括遗传学。本研究旨在探讨ELN和FMOD候选基因序列变异与ACL破裂的关系,基于这两个蛋白聚糖编码基因在维持组织结构完整性和调节纤维形成方面的重要生物学功能。材料和方法:参与者包括229名(164名男性和65名女性)手术诊断为ACL断裂(ACLR)并符合韧带重建条件的个体和192名(107名男性和85名女性)无ACL损伤史的健康参与者(CON组)。ACLR组所有229名参与者均通过非接触机制受伤。采用卡方检验对前交叉韧带破裂(ACLR)组与对照组(CON)的ELN rs2071307和FMOD rs7543148进行相关性分析。结果:从研究中可以看出,运动员被测组在ELN rs2071307基因多态性中AA基因型的出现频率明显高于对照组。然而,从性别上看,人们可以观察到,这种情况明显更频繁。在FMOD rs7543148基因多态性中,研究组TT基因型明显少于对照组,与之前的多态性相似,男性组TT基因型明显少于对照组。结论:体育运动中的基因研究,特别是与选定基因的特征多态性变异有关的损伤,是合理的,特别是在性别同质群体中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
17
审稿时长
30 weeks
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