PMID- 17915152 OWN - NLM STAT- MEDLINE DCOM- 20071102 LR - 20190917 IS - 1579-2242 (Electronic) IS - 0300-8932 (Linking) VI - 60 IP - 9 DP - 2007 Sep TI - [Metalloproteases, vascular remodeling and atherothrombotic syndromes]. PG - 959-67 AB - Defects in the synthesis and breakdown of the extracellular matrix (ECM) are now seen as key processes in the development of atherosclerosis and its thrombotic complications. Correlations have been observed between circulating levels of ECM biomarkers and the clinical manifestations of and risk factors for atherosclerosis. Several matrix metalloproteinases (MMPs), endopeptidases that can degrade the ECM, such as MMP-9 and MMP-10, play important roles in the pathophysiology of atherothrombosis and contribute to the expansion of abdominal aortic aneurysms. Moreover, they may also be useful biomarkers of atherosclerotic risk and serve as predictors of coronary and cerebrovascular disease recurrence. Although at present the effect of tissue inhibitors of MMPs (TIMPs) on cardiovascular disease prognosis is still uncertain, the ECM could be a promising therapeutic target in atherothrombotic disease, and several MMP inhibitors are currently undergoing clinical trials. FAU - Rodriguez, Jose A AU - Rodriguez JA AD - Laboratorio de Aterosclerosis, Area de Ciencias Cardiovasculares, CIMA-Universidad de Navarra, Pamplona, Espana. josean@unav.es FAU - Orbe, Josune AU - Orbe J FAU - Paramo, Jose A AU - Paramo JA LA - spa PT - English Abstract PT - Journal Article PT - Review TT - Metaloproteasas, remodelado vascular y sindromes aterotromboticos. PL - Spain TA - Rev Esp Cardiol JT - Revista espanola de cardiologia JID - 0404277 RN - EC 3.4.- (Metalloproteases) SB - IM CIN - Rev Esp Cardiol. 2008 Mar;61(3):327; author reply 327-8. PMID: 18361910 MH - Atherosclerosis/*enzymology/*physiopathology MH - Blood Vessels/physiopathology MH - Extracellular Matrix/physiology MH - Humans MH - Metalloproteases/*physiology MH - Risk Factors MH - Syndrome MH - Thrombosis/*enzymology/*physiopathology RF - 89 EDAT- 2007/10/05 09:00 MHDA- 2007/11/06 09:00 CRDT- 2007/10/05 09:00 PHST- 2007/10/05 09:00 [pubmed] PHST- 2007/11/06 09:00 [medline] PHST- 2007/10/05 09:00 [entrez] AID - 13109649 [pii] AID - 10.1157/13109649 [doi] PST - ppublish SO - Rev Esp Cardiol. 2007 Sep;60(9):959-67. doi: 10.1157/13109649.