Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease

被引:45
作者
Atiq, Ferdows [1 ]
Meijer, Karina [2 ]
Eikenboom, Jeroen [3 ,4 ]
Fijnvandraat, Karin [5 ]
Mauser-Bunschoten, Eveline P. [6 ]
van Galen, Karin P. M. [6 ]
Nijziel, Marten R. [7 ,8 ]
Ypma, Paula F. [9 ]
de Meris, Joke [10 ]
Laros-van Gorkom, Britta A. P. [7 ]
van der Bom, Johanna G. [11 ,12 ]
de Maat, Moniek P. [1 ]
Cnossen, Marjon H. [13 ]
Leebeek, Frank W. G. [1 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Haematol, POB 2040, NL-3000 CA Rotterdam, Netherlands
[2] Univ Groningen, Med Ctr Groningen, Dept Haematol, Groningen, Netherlands
[3] Leiden Univ, Med Ctr, Dept Thrombosis & Haemostasis, Leiden, Netherlands
[4] Leiden Univ, Med Ctr, Einthoven Lab Vasc & Regenerat Med, Leiden, Netherlands
[5] Emma Childrens Hosp, Acad Med Ctr, Pediat Haematol, Amsterdam, Netherlands
[6] Univ Utrecht, Univ Med Ctr, Van Creveldklin, Utrecht, Netherlands
[7] Radboud Univ Nijmegen, Med Ctr, Dept Haematol, Nijmegen, Netherlands
[8] Catharina Hosp, Dept Haematol, Eindhoven, Netherlands
[9] Haga Hosp, Dept Haematol, The Hague, Netherlands
[10] Netherlands Haemophilia Soc, Amsterdam, Netherlands
[11] Leiden Univ, Med Ctr, Dept Clin Epidemiol, Leiden, Netherlands
[12] Sanquin Res, Jon J van Rood Ctr Clin Transfus Med, Leiden, Netherlands
[13] Erasmus Univ, Sophia Childrens Hosp, Med Ctr, Dept Pediat Haematol, Rotterdam, Netherlands
关键词
VWD; VWF; diabetes; cancer; elderly; ABO BLOOD-GROUP; FACTOR-VIII; ADULT PATIENTS; PLASMA-LEVELS; RISK-FACTORS; DIAGNOSIS; CANCER; ATHEROSCLEROSIS; HYPOTHYROIDISM; CLASSIFICATION;
D O I
10.1111/bjh.15277
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Some comorbidities, such as hypertension, are associated with higher von Willebrand factor (VWF) levels in the general population. No studies have been conducted to assess this association in patients with von Willebrand disease (VWD). Therefore, we studied this association in patients with type 1 (n=333) and type 2 (n=203) VWD from the WiN study. VWF antigen (VWF:Ag) was higher in type 1 VWD patients with hypertension [difference: 023iu/ml, 95% confidence interval (CI): 011-035], diabetes mellitus (011iu/ml, 95% CI: -002 to 023), cancer (014iu/ml, 95% CI: 003-025) and thyroid dysfunction (014iu/ml, 95% CI: 003-026) than in patients without these comorbidities (all corrected for age, sex and blood group). Similar results were observed for VWF collagen binding capacity (VWF:CB), VWF activity as measured by the VWF monoclonal antibody assay (VWF:Ab) and factor VIII (FVIII) coagulant activity (FVIII:C). In type 1 VWD, age was associated with higher VWF:Ag (003iu/ml; 95% CI: 001-004), VWF:CB (002iu/ml; 95% CI: 000-004), VWF:Ab (004iu/ml; 95% CI: 002-006) and FVIII:C (003iu/ml; 95% CI: 001-006) per decade increase. After adjustment for relevant comorbidities, these associations were no longer significant. Despite the higher VWF and FVIII levels, type 1 VWD patients with comorbidities had more bleeding episodes, particularly during surgery. There was no association between comorbidities and VWF/FVIII levels or bleeding phenotype in type 2 VWD patients. In conclusion, comorbidities are associated with higher VWF and FVIII levels in type 1 VWD and may explain the age-related increase of VWF and FVIII levels.
引用
收藏
页码:93 / 105
页数:13
相关论文
共 51 条
[1]   Outgrowing the laboratory diagnosis of type 1 von Willebrand disease: A two decade study [J].
Abou-Ismail, Mouhamed Yazan ;
Ogunbayo, Gbolahan O. ;
Secic, Michelle ;
Kouides, Peter A. .
AMERICAN JOURNAL OF HEMATOLOGY, 2018, 93 (02) :232-237
[2]   Aging and ABO blood type influence von Willebrand factor and factor VIII levels through interrelated mechanisms [J].
Albanez, S. ;
Ogiwara, K. ;
Michels, A. ;
Hopman, W. ;
Grabell, J. ;
James, P. ;
Lillicrap, D. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2016, 14 (05) :953-963
[3]   Temporary relief of symptomatic von Willebrand disease by multiple myeloma [J].
Auwerda, JJA ;
Sonneveld, P ;
Leebeek, FWG .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2005, 3 (05) :1088-1089
[4]   Prothrombotic coagulation abnormalities in patients with newly diagnosed multiple myeloma [J].
Auwerda, Johannes J. A. ;
Sonneveld, Pieter ;
de Maat, Monica P. M. ;
Leebeek, Frank W. G. .
HAEMATOLOGICA, 2007, 92 (02) :279-280
[5]   von Willebrand factor fibers promote cancer-associated platelet aggregation in malignant melanoma of mice and humans [J].
Bauer, Alexander T. ;
Suckau, Jan ;
Frank, Kathrin ;
Desch, Anna ;
Goertz, Lukas ;
Wagner, Andreas H. ;
Hecker, Markus ;
Goerge, Tobias ;
Umansky, Ludmila ;
Beckhove, Philipp ;
Utikal, Jochen ;
Gorzelanny, Christian ;
Diaz-Valdes, Nancy ;
Umansky, Viktor ;
Schneider, Stefan W. .
BLOOD, 2015, 125 (20) :3153-3163
[6]   Platelet-dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH [J].
Bodo, I. ;
Eikenboom, J. ;
Montgomery, R. ;
Patzke, J. ;
Schneppenheim, R. ;
Di Paola, J. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2015, 13 (07) :1345-1350
[7]   Increase of von Willebrand factor with aging in type 1 von Willebrand disease: fact or fiction? [J].
Borghi, Mariachiara ;
Guglielmini, Giuseppe ;
Mezzasoma, Anna Maria ;
Falcinelli, Emanuela ;
Bury, Loredana ;
Malvestiti, Marco ;
Gresele, Paolo .
HAEMATOLOGICA, 2017, 102 (11) :E431-E433
[8]   Generation and validation of the Condensed MCMDM-1VWD Bleeding Questionnaire for von Willebrand disease [J].
Bowman, M. ;
Mundell, G. ;
Grabell, J. ;
Hopman, W. M. ;
Rapson, D. ;
Lillicrap, D. ;
James, P. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2008, 6 (12) :2062-2066
[9]   Endothelial function and dysfunction. Part II: Association with cardiovascular risk factors and diseases. A statement by the Working Group on Endothelins and Endothelial Factors of the European Society of Hypertension [J].
Brunner, H ;
Cockcroft, JR ;
Deanfield, J ;
Donald, A ;
Ferrannini, E ;
Halcox, J ;
Kiowski, W ;
Luscher, TF ;
Mancia, G ;
Natali, A ;
Oliver, JJ ;
Pessina, AC ;
Rizzoni, D ;
Rossi, GP ;
Salvetti, A ;
Spieker, LE ;
Taddei, S ;
Webb, DJ .
JOURNAL OF HYPERTENSION, 2005, 23 (02) :233-246
[10]  
Clark P, 1998, THROMB HAEMOSTASIS, V79, P1166