COL27A1和COL11A1基因变异与波兰运动员前交叉韧带断裂易感性无关

IF 0.7 Q4 SPORT SCIENCES
Zhuo Sun, Aleksandra Bojarczuk, P. Cięszczyk
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引用次数: 0

摘要

前言:运动损伤是导致前交叉韧带(ACL)断裂最常见的原因。先前的研究已经证明了COL27A1和COL11A1基因变异与肌肉骨骼软组织损伤之间的联系。然而,之前没有研究调查COL27A1 rs1570460和COL11A1 rs3753841在任何人群中ACL破裂的情况。因此,我们的研究旨在评估特定单核苷酸多态性(snp),即COL27A1 rs946053和COL11A1 rs3753841与波兰运动员队列中ACL损伤(ACL- i)发生之间的关系。方法:研究纳入233名患有ACL-I的运动员(男161人,女71人)和228名没有ACL-I病史的健康对照组运动员(男143人,女85人)。进行基因分型以评估COL27A1 rs946053和COL11A1 rs3753841遗传变异的存在。使用R编程环境和软件包进行统计分析,并在四种遗传模型中测试snp与acl - 1之间的关联:显性、共显性、隐性和过显性。结果:所有分析的多态性均符合Hardy-Weinberg平衡(HWE)。研究显示acl - 1组与对照组之间无显著差异。结论:尽管本研究中所调查的snp与ACL-I之间没有显著关联,但我们的发现强调了继续研究以揭示导致ACL-I的精确遗传风险机制和病因的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The COL27A1 and COL11A1 gene variants are not associated with the susceptibility to anterior cruciate ligament rupture in Polish athletes
Introduction: Sports injuries are the most common cause of anterior cruciate ligament (ACL) ruptures. Previous research has demonstrated links between some of the COL27A1 and COL11A1 genetic variants and musculoskeletal soft tissue injuries. However, no previous research has investigated the COL27A1 rs1570460 and the COL11A1 rs3753841 in the context of ACL rupture in any population. Thus, our study aimed to assess the association between specific single nucleotide polymorphisms (SNPs), i.e., COL27A1 rs946053 and COL11A1 rs3753841, and the occurrence of ACL injury (ACL-I) in a cohort of Polish athletes. Methods: The study enrolled 233 athletes with ACL-I (161 males and 71 females) and 228 healthy control athletes (143 males and 85 females) with no prior ACL-I history. Genotyping was conducted to assess the presence of COL27A1 rs946053 and COL11A1 rs3753841 genetic variants. Statistical analyses were performed using the R programming environment and package, and an association between SNPs and ACL-I was tested in four genetic models: dominant, co-dominant recessive, and over-dominant. Results: All the analyzed polymorphisms conformed to Hardy-Weinberg equilibrium (HWE). The study revealed no significant differences between the ACL-I and control groups. Conclusions: Despite the absence of significant associations between the investigated SNPs and ACL-I in this study, our findings highlight the importance of continued research to unravel the precise genetic risk mechanisms and etiological factors contributing to ACL-I.
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CiteScore
1.50
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0.00%
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17
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30 weeks
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