Abstract

Von Willebrand factor (VWF) is a multimeric plasma glycoprotein that plays a central role in the initiation of blood coagulation. Through interactions between its specific functional domains, the vascular wall, coagulation factor VIII, and platelet receptors, VWF maintains hemostasis by binding to platelets and delivering factor VIII to the sites of vascular injury. In the healthy human population, plasma VWF levels vary widely. The important role of VWF is illustrated by individuals at the extremes of the normal distribution of plasma VWF concentrations where individuals with low VWF levels are more likely to present with mucocutaneous bleeding. Conversely, people with high VWF levels are at higher risk for venous thromboembolic disease, stroke, and coronary artery disease. This report will summarize recent advances in our understanding of environmental influences and the genetic control of VWF plasma variation in healthy and symptomatic populations and will also highlight the unanswered questions that are currently driving this field of study.

Highlights

  • Genetic studies of plasma von Willebrand factor (VWF) variation are a paradigm for the genetic regulation of quantitative traits

  • While other important medical diseases such as type II diabetes and coronary artery disease rely on descriptive clinical phenotyping and arose relatively recently in human populations, plasma VWF levels are an measured proxy for bleeding or thrombosis risk, which are two traits with likely high selective pressures in human evolution

  • These pressures may have led to a genetic architecture where a relatively limited number of genes determine plasma VWF levels compared with several hundreds of genes that have been associated with other complex traits, such as human height variation[2]

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Summary

Karl C Desch

Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan, USA v1 First published: 23 Jan 2018, 7(F1000 Faculty Rev):[96] ( https://doi.org/10.12688/f1000research.13056.1) Latest published: 23 Jan 2018, 7(F1000 Faculty Rev):[96] ( https://doi.org/10.12688/f1000research.13056.1)

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