[Von Willebrand factor, endothelial lesion, and ischemic heart disease]. 2008

B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
Servicio de Medicina Intensiva, Hospital Universitario Miguel Servet, Zaragoza, España. beaagus@wanadoo.es

OBJECTIVE To analyze if the levels of von Willebrand factor (FvW) are higher in patients with ischemic heart disease than in healthy subjects and evaluate the relationship of these levels with clinical recurrence and coronary interventionism. METHODS Observational prospective study. METHODS We analyzed the levels of FvW in 75 patients with ischemic heart disease who underwent coronary interventionism (Group I) and compared them with those of 30 healthy subjects with no cardiovascular risk factors and who, theoretically, had no coronary injuries (Group II). METHODS Levels of FvW before coronary interventionism (sample 0), 24 hours after (sample 1), and at three months of out-patient follow-up (sample 2). A single measurement was made of the FvW levels in Group II. RESULTS Subjects with ischemic heart disease had higher levels of FvW than healthy subjects (162+/-74% versus 95+/-33%; p=0.0001). FvW levels were significantly increased after coronary interventionism (162.4+/-74.9% in sample 0 versus 213+/-90% in sample 1; p=0.0001). Patients with clinical symptoms at three months have no significant difference regarding those with no symptoms in the FvW levels (125+/-63% versus 133+/-60%; p=0.57). CONCLUSIONS FvW levels reflect an endothelial alteration in patients with ischemic heart disease. The increase of the levels after coronary interventionism could be due to the endothelial aggression itself of the intervention. It was not possible to demonstrate higher levels of FvW in patients with symptoms in the three month follow-up.

UI MeSH Term Description Entries
D008297 Male Males
D011446 Prospective Studies Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group. Prospective Study,Studies, Prospective,Study, Prospective
D004730 Endothelium, Vascular Single pavement layer of cells which line the luminal surface of the entire vascular system and regulate the transport of macromolecules and blood components. Capillary Endothelium,Vascular Endothelium,Capillary Endotheliums,Endothelium, Capillary,Endotheliums, Capillary,Endotheliums, Vascular,Vascular Endotheliums
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D014841 von Willebrand Factor A high-molecular-weight plasma protein, produced by endothelial cells and megakaryocytes, that is part of the factor VIII/von Willebrand factor complex. The von Willebrand factor has receptors for collagen, platelets, and ristocetin activity as well as the immunologically distinct antigenic determinants. It functions in adhesion of platelets to collagen and hemostatic plug formation. The prolonged bleeding time in VON WILLEBRAND DISEASES is due to the deficiency of this factor. Factor VIII-Related Antigen,Factor VIIIR-Ag,Factor VIIIR-RCo,Plasma Factor VIII Complex,Ristocetin Cofactor,Ristocetin-Willebrand Factor,von Willebrand Protein,Factor VIII Related Antigen,Factor VIIIR Ag,Factor VIIIR RCo,Ristocetin Willebrand Factor
D017202 Myocardial Ischemia A disorder of cardiac function caused by insufficient blood flow to the muscle tissue of the heart. The decreased blood flow may be due to narrowing of the coronary arteries (CORONARY ARTERY DISEASE), to obstruction by a thrombus (CORONARY THROMBOSIS), or less commonly, to diffuse narrowing of arterioles and other small vessels within the heart. Severe interruption of the blood supply to the myocardial tissue may result in necrosis of cardiac muscle (MYOCARDIAL INFARCTION). Heart Disease, Ischemic,Ischemia, Myocardial,Ischemic Heart Disease,Disease, Ischemic Heart,Diseases, Ischemic Heart,Heart Diseases, Ischemic,Ischemias, Myocardial,Ischemic Heart Diseases,Myocardial Ischemias

Related Publications

B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
January 1988, Sovetskaia meditsina,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
May 2022, Haemophilia : the official journal of the World Federation of Hemophilia,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
December 2001, Reviews in clinical and experimental hematology,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
October 1987, Blood,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
January 2016, [Rinsho ketsueki] The Japanese journal of clinical hematology,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
January 2014, Nederlands tijdschrift voor geneeskunde,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
January 1993, Ocular immunology and inflammation,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
June 2006, Journal of thrombosis and haemostasis : JTH,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
April 1985, The Journal of clinical investigation,
B Virgós-Señor, and A Nebra-Puertas, and M A Suárez-Pinilla, and R Cornudella-Lacasa, and P Portero-Pérez
January 1986, Terapevticheskii arkhiv,
Copied contents to your clipboard!