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基质金属蛋白酶 3(MMP3)单核苷酸多态性与腱病的相关性:高水平运动员的病例对照研究。

Association of the matrix metalloproteinase 3 (MMP3) single nucleotide polymorphisms with tendinopathies: case-control study in high-level athletes.

机构信息

Genos Ltd, Borongajska cesta 83h, 10000, Zagreb, Croatia.

Faculty of Kinesiology, University of Zagreb, Horvaćanski zavoj 15, 10000, Zagreb, Croatia.

出版信息

Int Orthop. 2021 May;45(5):1163-1168. doi: 10.1007/s00264-020-04684-w. Epub 2020 Jun 30.

Abstract

BACKGROUND

Matrix metalloproteinases (MMPs) play an important role in matrix remodelling, as well as in tendon integrity. Due to overuse, athletes often develop chronic tendinopathies. If not treated, they lead to severe impairment, even complete tendon ruptures.

AIM

The main purpose of this study was to investigate whether three functional polymorphisms within the MMP3 gene are associated with increased risk of developing tendinopathies in high-level Croatian athletes.

METHODS

We have recruited one hundred fifty-five (63 high-level athletes with diagnosed tendinopathies and 92 asymptomatic controls) unrelated Caucasians for this case-control genetic study. All participants were genotyped for three single nucleotide polymorphisms (SNP) within the MMP3 gene: rs591058 C/T, rs650108 A/G and rs679620 G/A using the pyrosequencing method.

RESULTS

The MMP3 rs650108 GG (P = 0.0074) and rs679620 AA (P = 0.0119) genotypes were significantly over-represented in cases compared with controls, while rs591058 TT (P = 0.0759), as well as haplotype variant T - G - A (P = 0.06), implicated that there is an indication of predisposition for tendinopathies.

CONCLUSION

These results support association between functional variants within the MMP3 gene and the risk of tendinopathies in high-level athletes. Further research is needed to replicate these results in a larger population.

摘要

背景

基质金属蛋白酶(MMPs)在基质重塑以及肌腱完整性中发挥着重要作用。由于过度使用,运动员经常会患上慢性腱病。如果不加以治疗,它们会导致严重的损伤,甚至完全肌腱断裂。

目的

本研究的主要目的是研究 MMP3 基因内的三个功能多态性是否与克罗地亚高水平运动员腱病发病风险增加有关。

方法

我们进行了这项病例对照遗传研究,共招募了 155 名(63 名患有腱病的高水平运动员和 92 名无症状对照者)无关的白种人。所有参与者均采用焦磷酸测序法对 MMP3 基因内的三个单核苷酸多态性(SNP)进行基因分型:rs591058 C/T、rs650108 A/G 和 rs679620 G/A。

结果

与对照组相比,MMP3 rs650108 GG(P=0.0074)和 rs679620 AA(P=0.0119)基因型在病例中明显过表达,而 rs591058 TT(P=0.0759)以及 T-G-A 单倍型变异(P=0.06)表明存在腱病易感性的迹象。

结论

这些结果支持 MMP3 基因内功能变体与高水平运动员腱病风险之间的关联。需要进一步的研究来在更大的人群中复制这些结果。

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