Inhibitory Effect of TIMP Influences the Morphology of Varicose Veins

Abstract Objectives Imbalance of matrix metalloproteinase enzymes (MMP) and their inhibitors (TIMPs) may contribute to the development of varicose veins. We hypothesised that, histological changes in varicose vein wall correlate with alterations in expression of MMP/TIMP. Methods Varicose veins ( n...

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Veröffentlicht in:European journal of vascular and endovascular surgery 2010-12, Vol.40 (6), p.754-765
Hauptverfasser: Aravind, B, Saunders, B, Navin, T, Sandison, A, Monaco, C, Paleolog, E.M, Davies, A.H
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Sprache:eng
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Zusammenfassung:Abstract Objectives Imbalance of matrix metalloproteinase enzymes (MMP) and their inhibitors (TIMPs) may contribute to the development of varicose veins. We hypothesised that, histological changes in varicose vein wall correlate with alterations in expression of MMP/TIMP. Methods Varicose veins ( n  = 26) were compared with great saphenous vein (GSV) segments ( n  = 11) from arterial bypass, and with arm and neck veins from fistula and carotid operations ( n  = 13). Varicose vein wall thickness was measured, enabling categorisation as atrophic and hypertrophic. MMP-2, MT1-MMP, TIMP-2, and TIMP-3 expression were quantitatively analysed by immunohistochemistry. Results There was significantly higher expression of TIMP-2 (immunopositive area 4.34% versus 0.26%), linked with connective tissue accumulation in the tunica media of varicose veins as compared with arm and neck vein controls. TIMP-2 and TIMP-3 expression was higher in hypertrophic than atrophic segments (3.2% versus 0.99% for TIMP-2, 1.7% versus 0.08% for TIMP-3). Similarly, TIMP-2 and TIMP-3 had elevated expression in the thicker proximal varicose vein segments compared to distal (4.3% versus 1.3% for TIMP-2 and 0.94% versus 0.41% for TIMP-3). Conclusions This study linked morphological changes in varicose vein walls with MMP/TIMP balance. A higher TIMP expression favours deposition of connective tissue and thus thicker vein wall, reducing matrix turnover by suppression of protease activity.
ISSN:1078-5884
1532-2165
DOI:10.1016/j.ejvs.2010.04.028