P2-17: Collagenase-1 and arterial hypertension in patients with metabolic syndrome - 12/02/16
Collagenase-1 et hypertension artérielle chez les patients ayant le syndrome métabolique
Résumé |
Background |
The aim of this study was to determine the collagenase-1 also named metalloproteinase-1 (MMP-1) and its tissue inhibitors, TIMP-1 and TIMP-2 in patients with metabolic syndrome (MetS) and to understand their relationship with the elevated blood pressure.
Methods |
199 patients with MetS and 150 control subjects were required in the Rabta hospital of Tunis. MMP-1, TIMP-1 and TIMP-2 levels were determined in citrate plasma by ELISA methods.
Results |
Levels of MMP-1 decreases significantly in MetS patients compared to control group (p<0.001) in contrast with TIMP-1 which was significantly higher in MetS patients compared to control group (p<0.001). A significant decrease in the levels of MMP-1 and the MMP-1/TIMP-1 ratio was found according to the elevated blood pressure in patients with MetS (p<0.001). Conversely, the TIMP-1 levels increase significantly with high blood pressure (p<0.001). In correlation analysis, negative correlations has been reported between MMP-1 and SBP (Systolic blood pressure) (r=−0.275, p<0.001) and between MMP-1 and DBP (Diastolic blood pressure) (r=−0.298, p<0.001) in patients with MetS. In contrast, the TIMP-1 is positively correlated with the same parameters (r=0.143, p=0.009; r=0.168, p=0.002). The MMP-1/TIMP-1 and MMP-1/TIMP-2 ratios shows the same correlations as those found between MMP-1 and these parameters (r=−0.284, p<0.001; r=− 0.185, p<0.001). According to the linear regression analysis, decreased levels of MMP-1 are independent of the increase in blood pressure.
Conclusions |
The decrease of the MMP-1 is associated with a significant increase of its specific inhibitor when blood pressure is high in patients with MetS. These results demonstrate the disruption of the balance between MMPs and their inhibitors and a matrix remodeling that may explain the pathophysiological changes in MetS and the elevated cardiovascular risk.
Le texte complet de cet article est disponible en PDF.Vol 64 - N° S1
P. S28 - décembre 2015 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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