von Willebrand Factor in Plasma and Urine of Men with Premature Coronary Artery Disease

Summary Plasma and urine samples from 17 men who had suffered a myocardial infarction before the age of 45 years were quantitatively and qualitatively analyzed for von Willebrand factor antigen (vWF), and compared with samples obtained from controls. The levels of vWF in plasma and its characteristic multimeric composition in the patient samples were not different from those of the controls. However, when analyzed for lower molecular weight components, plasma samples from some patients contained more degraded material than those of the controls as indicated by the presence of an extra protein band of vWF related material having a molecular weight of about 200 kDa. The levels in urine of vWF and the molecular weight of the fragments excreted did not differ between patients and controls. A relative increase in excretion of lower molecular fragments was, however, observed in the patient group. In a second group of 97 consecutive post-infarction patients under the age of 45 years the extra 200 kDa vWF band was found in 46% of the patients, whereas it was not detected in control plasmas. Taken together these findings suggest that degraded forms of vWF occur in normal plasma and that a more extensive degradation may occur in patients with coronary atherosclerosis, which could account for the relative increase in the excretion of lower molecular weight fragments observed in these patients.

[1]  M. Blombäck,et al.  Coagulation, fibrinolysis, and kallikrein systems in sepsis: relation to outcome. , 1989, Critical care medicine.

[2]  A. Woolf,et al.  Factor VIII related antigen in the assessment of vasculitis. , 1987, Annals of the rheumatic diseases.

[3]  T. Yamamoto,et al.  von Willebrand factor antigen in urine. , 1987, Thrombosis research.

[4]  T. Yamamoto,et al.  Application of an enzyme-linked immunosorbent assay (ELISA) to von Willebrand factor (vWF) and its derivatives. , 1986, Thrombosis research.

[5]  A. Hamsten,et al.  Relationship of angiographically defined coronary artery disease to serum lipoproteins and apolipoproteins in young survivors of myocardial infarction. , 1986, Circulation.

[6]  I. Kjønniksen,et al.  Visualization of von Willebrand Factor Multimers by Enzyme-Conjugated Secondary Antibodies , 1986, Thrombosis and Haemostasis.

[7]  Z. Ruggeri,et al.  Subunit composition of plasma von Willebrand factor. Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE). , 1986, The Journal of clinical investigation.

[8]  K. Mettinger A study of hemostasis in ischemic cerebrovascular disease: IV. A five year follow-up of some blood coagulation parameters also including fibrinopeptide A, factor XII and prekallikrein. , 1982, Thrombosis research.

[9]  A. Bloom The biosynthesis of factor VIII. , 1979, Clinics in haematology.

[10]  V. Fuster,et al.  Resistance to arteriosclerosis in pigs with von Willebrand's disease. Spontaneous and high cholesterol diet-induced arteriosclerosis. , 1978, The Journal of clinical investigation.

[11]  J. Erikssen,et al.  Plasma Antithrombin III and Factor VIII Antigen in Relation to Angiographic Findings, Angina and Blood Groups in Middle-Aged Men , 1977, Thrombosis and Haemostasis.

[12]  D. Heinegård,et al.  Determination of serum creatinine by a direct colorimetric method. , 1973, Clinica chimica acta; international journal of clinical chemistry.

[13]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.