Investigation of association between genetic polymorphisms of MMP2, MMP8, MMP9 and TIMP2 and development of varicose veins in the Slovak Population - pilot study
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
33471544
PubMed Central
PMC8603714
DOI
10.33549/physiolres.934597
PII: 934597
Knihovny.cz E-resources
- MeSH
- Adult MeSH
- Genetic Predisposition to Disease MeSH
- Genotype MeSH
- Polymorphism, Single Nucleotide MeSH
- Middle Aged MeSH
- Humans MeSH
- Matrix Metalloproteinase 2 genetics MeSH
- Matrix Metalloproteinase 8 genetics MeSH
- Matrix Metalloproteinase 9 genetics MeSH
- Matrix Metalloproteinases genetics MeSH
- Adolescent MeSH
- Young Adult MeSH
- Pilot Projects MeSH
- Promoter Regions, Genetic MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Tissue Inhibitor of Metalloproteinase-2 genetics MeSH
- Varicose Veins epidemiology genetics pathology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Slovakia epidemiology MeSH
- Names of Substances
- Matrix Metalloproteinase 2 MeSH
- Matrix Metalloproteinase 8 MeSH
- Matrix Metalloproteinase 9 MeSH
- Matrix Metalloproteinases MeSH
- MMP2 protein, human MeSH Browser
- MMP8 protein, human MeSH Browser
- MMP9 protein, human MeSH Browser
- TIMP2 protein, human MeSH Browser
- Tissue Inhibitor of Metalloproteinase-2 MeSH
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.
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