Department of Orthopedics, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, Changzhou 213000, China.
Department of Orthopedic Surgery, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310000, China.
Biosci Rep. 2019 Oct 30;39(10). doi: 10.1042/BSR20191549.
An association of Matrix Metalloproteinases-1/3 (MMP-1/3) rs1799750/rs3025058 polymorphism with increased risk of rotator cuff tear (RCT) has been reported in a Brazilian population. However, this significant association has not been confirmed in the Chinese population. Genotyping was conducted by polymerase chain reaction (PCR)-restriction fragment length polymorphism and direct sequencing. Our results demonstrated that individuals with the TT genotype had a significantly higher risk of RCT compared with those with the CC genotype. The increased risk of RCT progression was associated with the 2G allele of the rs1799750 polymorphism. No significant association was observed for genotypic and allelic frequencies of the rs3025058 polymorphism. A significant association of the MMP-1 rs1799750 polymorphism was observed with smokers, drinkers and people aged ≥60 years and non-diabetic people. Additionally, the MMP-1 rs1799750 polymorphism was associated with pre-operative stiffness in RCT patients. In conclusion, a significant correlation was identified between the MMP-1 rs1799750 polymorphism and RCT. The MMP-1 rs1799750 polymorphism might be considered as a biomarker of genetically high-risk RCT, helping to clarify the mechanism of RCT.
基质金属蛋白酶-1/3(MMP-1/3)rs1799750/rs3025058 多态性与肩袖撕裂(RCT)风险增加的关联在巴西人群中已有报道。然而,这种显著的关联尚未在中国人群中得到证实。基因分型采用聚合酶链反应(PCR)-限制性片段长度多态性和直接测序法。我们的结果表明,与 CC 基因型相比,TT 基因型个体发生 RCT 的风险显著增加。rs1799750 多态性的 2G 等位基因与 RCT 进展的风险增加相关。rs3025058 多态性的基因型和等位基因频率无显著相关性。MMP-1 rs1799750 多态性与吸烟者、饮酒者和年龄≥60 岁者以及非糖尿病患者显著相关。此外,MMP-1 rs1799750 多态性与 RCT 患者术前僵硬有关。总之,MMP-1 rs1799750 多态性与 RCT 之间存在显著相关性。MMP-1 rs1799750 多态性可能被认为是遗传高风险 RCT 的生物标志物,有助于阐明 RCT 的发病机制。