Department of Medical Biology, Jessenius Faculty of Medicine, Martin, Slovakia.
Physiol Res. 2020 Dec 31;69(Suppl 3):S443-S454. doi: 10.33549/physiolres.934597.
Matrix metalloproteinases (MMPs) are a family of zinc-dependent metalloendopeptidases that degrades extracellular matrix (ECM) components. MMPs are associated with venous wall remodelling, proliferation, migration, phenotypic and functional transformation of vascular smooth muscle cells and ECM organization under the physiological and pathophysiological conditions. We investigated possible association of genetic promoter polymorphisms of MMP2 (rs243866), MMP8 (rs11225395), MMP9 (rs3918242) and TIMP2 (rs8179090) to varicose veins development in the Slovak population. Genomic DNA from 276 Slovak individuals (138 cases, 138 controls) was genotyped for selected SNPs (rs243866, rs11225395, rs3918242 and rs8179090) using the PCR-RFLP analysis. The data were analysed by chi-squared (chi2) test, logistic regression, and Mann-Whitney test. The risk of varicose veins development was evaluated in dominant, codominant and recessive genetic models. The statistical evaluation of selected polymorphisms in patients in all three genetic models has not shown a significant risk of varicose veins development. Our study has not shown the association between selected polymorphisms and increased risk of varicose veins development in Slovak population. More evidence with broaden sample size is needed.
基质金属蛋白酶(MMPs)是一组锌依赖性金属内肽酶,可降解细胞外基质(ECM)成分。在生理和病理生理条件下,MMPs 与静脉壁重塑、增殖、迁移、血管平滑肌细胞的表型和功能转化以及 ECM 组织有关。我们研究了 MMP2(rs243866)、MMP8(rs11225395)、MMP9(rs3918242)和 TIMP2(rs8179090)基因启动子多态性与斯洛伐克人群静脉曲张发展之间的可能关联。使用 PCR-RFLP 分析,对来自 276 名斯洛伐克个体(138 例病例,138 例对照)的基因组 DNA 进行了选定 SNP(rs243866、rs11225395、rs3918242 和 rs8179090)的基因分型。通过卡方检验(chi2 检验)、逻辑回归和曼-惠特尼检验对数据进行分析。在显性、共显性和隐性遗传模型中评估了静脉曲张发展的风险。在所有三种遗传模型中,对患者中选定的多态性进行的统计学评估并未显示静脉曲张发展的风险增加。我们的研究并未显示所选多态性与斯洛伐克人群静脉曲张发展风险增加之间存在关联。需要更多证据和更广泛的样本量。