Aging and ABO blood type influence von Willebrand factor and factor VIII levels through interrelated mechanisms.

scientific article published on 27 April 2016

Aging and ABO blood type influence von Willebrand factor and factor VIII levels through interrelated mechanisms. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/JTH.13294
P932PMC publication ID5949873
P698PubMed publication ID26875505

P2093author name stringP James
K Ogiwara
D Lillicrap
A Michels
J Grabell
W Hopman
S Albánez
P2860cites workThe influence of the ABO blood type on the distribution of von Willebrand factor in healthy children with no bleeding symptomsQ45730907
Plasma von Willebrand factor and arterial agingQ46447114
Heterogeneous detection of A-antigen on von Willebrand factor derived from platelets, endothelial cells and plasmaQ50237767
No evidence for a direct effect of von Willebrand factor's ABH blood group antigens on von Willebrand factor clearance.Q53619865
von Willebrand factor and its propeptide: the influence of secretion and clearance on protein levels and the risk of venous thrombosisQ59242720
Relation of the Prothrombotic State to Increasing Age (from the Framingham Offspring Study)Q59608032
The effect of exercise on von Willebrand factor and ADAMTS-13 in individuals with type 1 and type 2B von Willebrand diseaseQ59679399
Human Umbilical Vein Endothelial Cells Differ from Other Endothelial Cells in Failing to Express ABO Blood Group AntigensQ60034609
von Willebrand disease and aging: an evolving phenotypeQ62107242
Independent association of von Willebrand factor with surrogate markers of atherosclerosis in middle-aged asymptomatic subjectsQ62693846
Comparative study of the sugar chains of factor VIII purified from human plasma and from the culture media of recombinant baby hamster kidney cellsQ68101165
Human plasma alpha 2-macroglobulin and von Willebrand factor possess covalently linked ABO(H) blood group antigens in subjects with corresponding ABO phenotypeQ72087210
von Willebrand factor and its propeptide in children with diabetes. Relation between endothelial dysfunction and microalbuminuriaQ73023597
Von Willebrand factor propeptide in vascular disordersQ74314907
Von Willebrand factor in Italian centenariansQ78846136
ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigensQ80059284
Von Willebrand diseaseQ80994281
Correlation between von Willebrand factor antigen, von Willebrand factor ristocetin cofactor activity and factor VIII activity in plasmaQ81041403
Reassessment of ABO blood group, sex, and age on laboratory parameters used to diagnose von Willebrand disorder: potential influence on the diagnosis vs the potential association with risk of thrombosisQ82279339
Possible role of ABO system in age-related diseases and longevity: a narrative reviewQ21093222
Endothelium-based biomarkers are associated with cerebral malaria in Malawian children: a retrospective case-control studyQ28743878
Hemostasis factors and agingQ33299066
von Willebrand factor propeptide in vascular disorders: A tool to distinguish between acute and chronic endothelial cell perturbationQ33329307
Elevated Von Willebrand factor propeptide for the diagnosis of thrombotic microangiopathy and for predicting a poor outcomeQ33393270
Plasma ADAMTS13, von Willebrand factor (VWF) and VWF propeptide profiles in patients with DIC and related diseasesQ33398134
Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) ConsortiumQ33817075
Amount of H antigen expressed on circulating von Willebrand factor is modified by ABO blood group genotype and is a major determinant of plasma von Willebrand factor antigen levelsQ34113248
The effect of ABO blood group on the diagnosis of von Willebrand disease.Q34180946
Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival.Q35848737
ABO Blood Groups and Cardiovascular DiseasesQ36361023
Changes in von Willebrand factor level and von Willebrand activity with age in type 1 von Willebrand diseaseQ36369902
von Willebrand factor, endothelial dysfunction, and cardiovascular diseaseQ36481209
Hemostasis and agingQ36543985
ABO blood group determines plasma von Willebrand factor levels: a biologic function after all?Q36604393
Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD).Q36658007
ABO(H) blood groups and vascular disease: a systematic review and meta-analysis.Q36987171
von Willebrand factor in cardiovascular disease: focus on acute coronary syndromes.Q37112364
Von Willebrand factor, type 2 diabetes mellitus, and risk of cardiovascular disease: the framingham offspring studyQ37353655
von Willebrand factor to the rescue.Q37422872
Evolutionary aspects of ABO blood group in humansQ38358460
von Willebrand factor biosynthesis, secretion, and clearance: connecting the far endsQ38364984
Von Willebrand factor drives the association between elevated factor VIII and poor outcomes in patients with ischemic strokeQ39426411
Relation of ABO blood groups to the severity of coronary atherosclerosis: an Gensini score assessment.Q41739487
Structures of the asparagine-linked oligosaccharide chains of human von Willebrand factor. Occurrence of blood group A, B, and H(O) structuresQ41906702
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factorQ42524319
VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand diseaseQ42937413
Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case seriesQ43123377
Association of ABO(H) and I blood group system development with von Willebrand factor and Factor VIII plasma levels in children and adolescentsQ43138945
Aberrant expression of histo-blood group A type 3 antigens in vascular endothelial cells in inflammatory sitesQ43153106
Altered glycosylation of platelet-derived von Willebrand factor confers resistance to ADAMTS13 proteolysisQ43701770
Quantitative analysis of von Willebrand factor propeptide release in vivo: effect of experimental endotoxemia and administration of 1-deamino-8-D-arginine vasopressin in humansQ44638884
Generation and validation of the Condensed MCMDM-1VWD Bleeding Questionnaire for von Willebrand diseaseQ45145414
Relationship between ABO and Secretor genotype with plasma levels of factor VIII and von Willebrand factor in thrombosis patients and control individualsQ45192189
P433issue5
P304page(s)953-963
P577publication date2016-04-27
P1433published inJournal of Thrombosis and HaemostasisQ6296004
P1476titleAging and ABO blood type influence von Willebrand factor and factor VIII levels through interrelated mechanisms.
P478volume14

Reverse relations

cites work (P2860)
Q57456624A decreased and less sustained desmopressin response in hemophilia A carriers contributes to bleeding
Q92657008ADAMTS13 maintains cerebrovascular integrity to ameliorate Alzheimer-like pathology
Q104610460Acquired von Willebrand syndrome and factor VIII in patients with moderate to severe mitral regurgitation undergoing transcatheter mitral valve repair
Q64240724Analytical characterization and reference interval of an enzyme-linked immunosorbent assay for active von Willebrand factor
Q92983714Bleeding assessment tools to predict von Willebrand disease: Utility of individual bleeding symptoms
Q45874634Can you grow out of von Willebrand disease?
Q55617050Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease.
Q38690381Controversies in the diagnosis of Type 1 von Willebrand disease
Q33608224Diagnosis and Treatment of von Willebrand Disease and Rare Bleeding Disorders
Q38814362Discrepant platelet and plasma von Willebrand factor in von Willebrand disease patients with p.Pro2808Leufs*24.
Q38822601Elucidation of Factor VIII Activity Pharmacokinetics: A Pooled Population Analysis in Patients With Hemophilia A Treated With Moroctocog Alfa
Q33435117Histones link inflammation and thrombosis through the induction of Weibel-Palade body exocytosis
Q89774833Influence of blood group, von Willebrand factor levels, and age on factor VIII levels in non-severe haemophilia A
Q37733182Influences of ABO blood group, age and gender on plasma coagulation factor VIII, fibrinogen, von Willebrand factor and ADAMTS13 levels in a Chinese population.
Q99566288Intronic regions of the human coagulation factor VIII gene harboring transcription factor binding sites with a strong bias towards the short-interspersed elements
Q97551370Low VWF: insights into pathogenesis, diagnosis, and clinical management
Q48719553New insights into the non-hemostatic role of von Willebrand factor in endothelial protection
Q33436573PT-VWD posing diagnostic and therapeutic challenges - small case series.
Q90441308Physiological Roles of the von Willebrand Factor-Factor VIII Interaction
Q49246959Regulation of plasma von Willebrand factor.
Q89800067Significant decrease of von Willebrand factor and plasminogen activator inhibitor-1 by providing supplementation with selenium and coenzyme Q10 to an elderly population with a low selenium status
Q59511557The common single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance
Q89691100The impact of ABO blood type on the prevalence of portal vein thrombosis in patients with advanced chronic liver disease
Q58781583Von Willebrand disease in the elderly: clinical perspectives
Q30240214What have we learned from large population studies of von Willebrand disease?

Search more.