Quantitative analysis of von Willebrand factor and its propeptide in plasma in acquired von Willebrand syndrome

被引:0
作者
van Genderen, PJJ
Boertjes, RC
van Mourik, JA
机构
[1] Univ Hosp Dijkzigt, Dept Hematol, NL-3015 GD Rotterdam, Netherlands
[2] Netherlands Red Cross, Blood Transfus Serv, Cent Lab, Amsterdam, Netherlands
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R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Measurement of the von Willebrand factor (vWF) propeptide, also known as von Willebrand antigen II, has been suggested to be helpful in the discrimination of congenital von Willebrand disease type I from type 2 and in assessing the extent of activation of the endothelium. We performed a quantitative analysis of mature VWF and its propeptide in plasma in 8 patients with acquired von Willebrand syndrome (AvWS) and in 20 normal individuals. Mature vWF levels were significantly lower in AvWS as compared with normal individuals (13.4 +/- 3.5 vs 35.6 +/- 3.3 nM, p < 0.001). In contrast, propeptide levels were significantly higher in AvWS (11.4 +/- 1.1 vs 4.7 +/- 0.2 nM, p < 0.001), probably reflecting a compensatory increase in vWF synthesis or increased perturbation of the endothelium in AvWS. After treatment with DDAVP, propeptide and mature vWF levels rose 5-fold in AvWS, whereas propeptide levels were not altered by the infusion of a VWF concentrate or treatment with high dose intravenous immunoglobulins, indicating that plasma propeptide levels are a reliable reflection of VWF synthesis. Measurement of propeptide levels may provide additional:information in AvWS as to whether decreased levels of mature vWF ii the circulation are due to a decrease in synthesis or due to ar. accelerated removal of vWF from the circulation.
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页码:495 / 498
页数:4
相关论文
共 15 条
[1]   Quantitative analysis of von Willebrand factor propeptide release in vivo: Effect of experimental endotoxemia and administration of 1-deamino-8-D-arginine vasopressin in humans [J].
Borchiellini, A ;
Fijnvandraat, K ;
tenCate, JW ;
Pajkrt, D ;
vanDeventer, SJH ;
Pasterkamp, G ;
MeijerHuizinga, F ;
ZwartHuinink, L ;
Voorberg, J ;
vanMourik, JA .
BLOOD, 1996, 88 (08) :2951-2958
[2]   Acquired von Willebrand disease in patients with high platelet counts [J].
Budde, U ;
Van Genderen, PJJ .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1997, 23 (05) :425-431
[3]  
FAY PJ, 1993, THROMB HAEMOSTASIS, V70, P63
[4]   PROPOLYPEPTIDE OF VONWILLEBRAND-FACTOR CIRCULATES IN BLOOD AND IS IDENTICAL TO VONWILLEBRAND ANTIGEN-II [J].
FAY, PJ ;
KAWAI, Y ;
WAGNER, DD ;
GINSBURG, D ;
BONTHRON, D ;
OHLSSONWILHELM, BM ;
CHAVIN, SI ;
ABRAHAM, GN ;
HANDIN, RI ;
ORKIN, SH ;
MONTGOMERY, RR ;
MARDER, VJ .
SCIENCE, 1986, 232 (4753) :995-998
[5]   MONOCYTES ENHANCE ENDOTHELIAL VONWILLEBRAND-FACTOR RELEASE AND PROSTACYCLIN PRODUCTION WITH DIFFERENT KINETICS AND DEPENDENCY ON INTERCELLULAR CONTACT BETWEEN THESE 2 CELL-TYPES [J].
HAKKERT, BC ;
RENTENAAR, JM ;
VANMOURIK, JA .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 80 (04) :495-503
[6]  
MCCARROLL DR, 1984, BLOOD, V63, P532
[7]  
MCCARROLL DR, 1984, J LAB CLIN MED, V103, P704
[8]  
Scott J. P., 1995, Blood, V86, p196A
[9]  
STEL HV, 1984, BLOOD, V63, P1408
[10]  
VANGENDEREN PJJ, 1994, BLOOD, V84, P3378