Department of Orthopedics and Traumatology, University of São Paulo, São Paulo, SP, Brazil.
Scand J Med Sci Sports. 2014 Feb;24(1):220-3. doi: 10.1111/j.1600-0838.2012.01469.x. Epub 2012 Apr 9.
Posterior tibial tendon is particularly vulnerable and is responsible for much morbidity in sportspersons. Some patients have a predisposition without a clinically recognized cause, suggesting that individual characteristics, inclusive genetic inheritance, play an important role in tendinopathy. Matrix metalloproteinase (MMP)-8 is a proteinase capable of degrading a large amount of extracellular proteins, and influence degradation and remodeling of collagen. To determine whether the -799 polymorphism in the promoter of MMP-8 gene is associated with tendinopathy in posterior tibial tendon, 50 patients undergoing surgical procedures and anatomopathological diagnosis of degenerative lesions of the posterior tibial tendon and 100 control patients with posterior tibial tendon integrity and without signs of degeneration in magnetic resonance imaging were evaluated for the -799 MMP-8 polymorphism. There was a significant difference in the presence of the different alleles (P = 0.001) and genotype (P = 0.003) between the control group and the test group for the MMP-8 gene. The polymorphism at position -799 of the gene for MMP-8 is associated with tendinopathy primary posterior tibial tendon in the population studied. The results suggest that individuals with the T allele are at greater risk of developing tendinopathy.
后胫肌腱特别脆弱,是运动员患病的主要原因之一。一些患者存在无临床公认原因的易感性,这表明个体特征,包括遗传因素,在肌腱病中发挥着重要作用。基质金属蛋白酶(MMP)-8 是一种能够降解大量细胞外蛋白的蛋白酶,影响胶原的降解和重塑。为了确定 MMP-8 基因启动子中的 -799 多态性是否与后胫肌腱肌腱病有关,对 50 名接受手术和后胫肌腱退行性病变解剖病理诊断的患者和 100 名后胫肌腱完整且磁共振成像无退变迹象的对照组患者进行了 MMP-8-799 多态性评估。对照组和实验组之间不同等位基因(P=0.001)和基因型(P=0.003)的存在存在显著差异。在研究人群中,MMP-8 基因的 -799 位置多态性与原发性后胫肌腱病有关。结果表明,携带 T 等位基因的个体发生肌腱病的风险更高。