Profile of von Willebrand factor antigen and von Willebrand factor propeptide in an overall TIA and ischaemic stroke population and amongst subtypes

被引:12
作者
Tobin, W. O. [1 ,2 ]
Kinsella, J. A. [1 ,8 ]
Kavanagh, G. F. [1 ]
O'Donnell, J. S. [3 ]
McGrath, R. T. [3 ]
Tierney, S. [4 ,5 ]
Egan, B. [4 ,5 ]
Feeley, T. M. [4 ,5 ]
Coughlan, T. [6 ,7 ]
Collins, D. R. [6 ,7 ]
O'Neill, D. [6 ,7 ]
Murphy, S. J. X. [1 ,7 ]
Lim, S. J. [1 ,7 ]
Murphy, R. P. [1 ,7 ]
McCabe, D. J. H. [1 ,7 ,9 ,10 ]
机构
[1] Trinity Coll Dublin, Incorporating Natl Childrens Hosp, Adelaide & Meath Hosp, Vasc Neurol Res Fdn, Dublin, Ireland
[2] Mayo Clin, Coll Med, Dept Neurol, Rochester, MN USA
[3] Royal Coll Surgeons Ireland, Irish Ctr Vasc Biol, Dublin, Ireland
[4] Trinity Coll Dublin, Incorporating Natl Childrens Hosp, Adelaide & Meath Hosp, Dept Neurol, Dublin, Ireland
[5] Trinity Coll Dublin, Incorporating Natl Childrens Hosp, Adelaide & Meath Hosp, Dept Vasc Surg, Dublin, Ireland
[6] Trinity Coll Dublin, Incorporating Natl Childrens Hosp, Adelaide & Meath Hosp, Dept Age Related Hlth Care, Dublin, Ireland
[7] Trinity Coll Dublin, Incorporating Natl Childrens Hosp, Adelaide & Meath Hosp, Stroke Serv, Dublin, Ireland
[8] Univ Coll Dublin, St Vincents Univ Hosp, Dept Neurol, Elm Pk, Dublin 4, Ireland
[9] UCL Inst Neurol, Dept Clin Neurosci, Royal Free Campus, London, England
[10] Trinity Coll Dublin, Sch Med, Acad Unit Neurol, Dublin, Ireland
关键词
Von Willebrand factor; Von Willebrand factor propeptide; TIA; Stroke; Case-control; ANTIPLATELET RESPONSIVENESS TRAP; PLATELET COMPLEX-FORMATION; LATE PHASES; VASCULAR DISORDERS; ENDOTHELIAL-CELLS; CAROTID STENOSIS; ACTIVATION; ATTACK; ADAMTS13; VWF;
D O I
10.1016/j.jns.2017.02.045
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Von Willebrand factor propeptide (VWF:Ag II) is proposed to be a more sensitive marker of acute endothelial activation than von Willebrand factor antigen (VWF:Ag). Simultaneous data on VWF:Ag and VWF:Ag II profiles are very limited following TIA and ischaemic stroke. Methods: In this prospective, observational, case-control study, plasma VWF:Ag and VWF:Ag II levels were quantified in 164 patients <= 4 weeks of TIA or ischaemic stroke (baseline), and then >= 14 days (14d) and >= 90 days (90d) later, and compared with those from 27 healthy controls. TIA and stroke subtyping was performed according to the TOAST classification. The relationship between VWF:Ag and VWF:Ag II levels and platelet activation status was assessed. Results: 'Unadjusted' VWF:Ag and VWF:Ag II levels were higher in patients at baseline, 14d and 90d than in controls (p <= 0.03). VWF:Ag levels remained higher in patients than controls at baseline (p <= 0.03), but not at 14d or 90d after controlling for differences in age or hypertension, and were higher in patients at baseline and 90d after controlling for smoking status (p <= 0.04). 'Adjusted' VWF:Ag II levels were not higher in patients than controls after controlling for age, hypertension or smoking (p >= 0.1). Patients with symptomatic carotid stenosis (N = 46) had higher VWF:Ag and VWF:Ag II levels than controls at all time-points (p <= 0.002). There was no significant correlation between platelet activation status and VWF:Ag or VWF:Ag II levels. Conclusions: VWF:Ag and VWF:Ag II levels are increased in an overall TIA and ischaemic stroke population, especially in patients with recently symptomatic carotid stenosis. VWF:Ag II was not superior to VWF:Ag at detecting acute endothelial activation in this cohort and might reflect timing of blood sampling in our study. (C) 2017 Elsevier B.V. All rights reserved.
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收藏
页码:404 / 410
页数:7
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