Changes in activities of circulating MMP-2 and MMP-9 in patients suffering from heart failure in relation to gender, hypertension and treatment: a cross-sectional study
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
27643937
DOI
10.33549/physiolres.933412
PII: 933412
Knihovny.cz E-resources
- MeSH
- Antihypertensive Agents therapeutic use MeSH
- Hypertension blood complications drug therapy MeSH
- Middle Aged MeSH
- Humans MeSH
- Matrix Metalloproteinase 2 blood MeSH
- Matrix Metalloproteinase 9 blood MeSH
- Cross-Sectional Studies MeSH
- Aged MeSH
- Sex Factors MeSH
- Heart Failure blood complications MeSH
- Case-Control Studies MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antihypertensive Agents MeSH
- Matrix Metalloproteinase 2 MeSH
- Matrix Metalloproteinase 9 MeSH
- MMP2 protein, human MeSH Browser
- MMP9 protein, human MeSH Browser
Matrix metalloproteinases (MMPs) play an important role in the pathogenesis of heart failure (HF). Our aim was to determine the activities of circulating MMP-2 and MMP-9 in patients with HF in respect of gender, comorbidities and treatment (n=51). We did not reveal any differences in circulating pro-MMP-2 and pro-MMP-9 activities between the patients with HF and without it. However, there was a decrease in activity of pro-MMP-2 in treated hypertensive participants versus healthy ones. In contrast, we observed increased pro-MMP-2 activity in hypertensive participants with coexistent HF versus hypertensive participants without HF. In addition, a decrease in pro-MMP-2 activity was shown in women suffering from HF versus men suffering from HF. In conclusion, potential inhibitory effect of antihypertensive treatment on pro-MMP-2 activity was found. Coexistent HF with hypertension probably reduces the inhibitory effect of antihypertensive treatment on pro-MMP-2 activity. Our data also suggest the role of potential cardioprotective factors influencing the activity of pro-MMP-2 in women.
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