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Increased von Willebrand factor parameters in children with febrile seizures

INTRODUCTION: Primary blood coagulation and wound sealing are orchestrated by von Willebrand factor (VWF), a large multimeric glycoprotein. Upon release of arginine vasopressin (AVP), VWF containing high molecular weight multimers is secreted. By measuring copeptin, the C-terminal part of the AVP pr...

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Autores principales: Pechmann, Astrid, Wellmann, Sven, Stoecklin, Benjamin, Krüger, Marcus, Zieger, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317815/
https://www.ncbi.nlm.nih.gov/pubmed/30605489
http://dx.doi.org/10.1371/journal.pone.0210004
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author Pechmann, Astrid
Wellmann, Sven
Stoecklin, Benjamin
Krüger, Marcus
Zieger, Barbara
author_facet Pechmann, Astrid
Wellmann, Sven
Stoecklin, Benjamin
Krüger, Marcus
Zieger, Barbara
author_sort Pechmann, Astrid
collection PubMed
description INTRODUCTION: Primary blood coagulation and wound sealing are orchestrated by von Willebrand factor (VWF), a large multimeric glycoprotein. Upon release of arginine vasopressin (AVP), VWF containing high molecular weight multimers is secreted. By measuring copeptin, the C-terminal part of the AVP prohormone, we recently found strongly increased AVP levels in children with febrile seizures (FS) as compared to children with fever but without seizures. It is unknown if increased AVP levels in FS are of any biological function. Therefore, our a priori hypothesis was that children with FS have increased VWF parameters in parallel with higher AVP levels. METHODS: We conducted a prospective, cross-sectional study of children aged between 6 months and 5 years. Children that presented at our emergency department with fever or a recent FS (within four hours) were evaluated to be included to the study. We measured serum copeptin and VWF parameters, including analyses of VWF:Antigen (WVF:Ag), VWF:collagen binding activity (VWF:CB) and VWF multimers in children with FS, febrile infections without seizures and additionally, in a non-febrile control group. RESULTS: We included 54 children in our study, 30 with FS, 10 in the febrile control group, and 14 in the non-febrile control group. Serum copeptin levels were significantly higher in children with FS (median [IQR] 24.73 pmol/l [13.65–68.65]) compared to the febrile control group (5.66 pmol/l [4.15–8.07], p = 0.002) and the non-febrile control group (4.78 pmol/l [3.33–5.3], p<0.001). VWF:CB levels were also significantly higher in children with FS (VWF:CB 2.29 U/ml [1.88–2.97]) as compared to the febrile (VWF:CB 1.41 U/ml [1.27–1.93], p = 0.048) and the non-febrile control group (VWF:CB 1.15 U/ml [0.98–1.21], p<0.001). VWF:Ag tended to be higher in children with FS compared to both control groups. Multivariate regression analysis revealed FS and copeptin as major determinants of VWF:CB. CONCLUSIONS: Our results suggest that increased secretion of AVP in children with FS is associated with higher plasma levels of VWF parameters. Especially VWF:CB may serve as additional biomarker in the diagnosis of FS.
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spelling pubmed-63178152019-01-19 Increased von Willebrand factor parameters in children with febrile seizures Pechmann, Astrid Wellmann, Sven Stoecklin, Benjamin Krüger, Marcus Zieger, Barbara PLoS One Research Article INTRODUCTION: Primary blood coagulation and wound sealing are orchestrated by von Willebrand factor (VWF), a large multimeric glycoprotein. Upon release of arginine vasopressin (AVP), VWF containing high molecular weight multimers is secreted. By measuring copeptin, the C-terminal part of the AVP prohormone, we recently found strongly increased AVP levels in children with febrile seizures (FS) as compared to children with fever but without seizures. It is unknown if increased AVP levels in FS are of any biological function. Therefore, our a priori hypothesis was that children with FS have increased VWF parameters in parallel with higher AVP levels. METHODS: We conducted a prospective, cross-sectional study of children aged between 6 months and 5 years. Children that presented at our emergency department with fever or a recent FS (within four hours) were evaluated to be included to the study. We measured serum copeptin and VWF parameters, including analyses of VWF:Antigen (WVF:Ag), VWF:collagen binding activity (VWF:CB) and VWF multimers in children with FS, febrile infections without seizures and additionally, in a non-febrile control group. RESULTS: We included 54 children in our study, 30 with FS, 10 in the febrile control group, and 14 in the non-febrile control group. Serum copeptin levels were significantly higher in children with FS (median [IQR] 24.73 pmol/l [13.65–68.65]) compared to the febrile control group (5.66 pmol/l [4.15–8.07], p = 0.002) and the non-febrile control group (4.78 pmol/l [3.33–5.3], p<0.001). VWF:CB levels were also significantly higher in children with FS (VWF:CB 2.29 U/ml [1.88–2.97]) as compared to the febrile (VWF:CB 1.41 U/ml [1.27–1.93], p = 0.048) and the non-febrile control group (VWF:CB 1.15 U/ml [0.98–1.21], p<0.001). VWF:Ag tended to be higher in children with FS compared to both control groups. Multivariate regression analysis revealed FS and copeptin as major determinants of VWF:CB. CONCLUSIONS: Our results suggest that increased secretion of AVP in children with FS is associated with higher plasma levels of VWF parameters. Especially VWF:CB may serve as additional biomarker in the diagnosis of FS. Public Library of Science 2019-01-03 /pmc/articles/PMC6317815/ /pubmed/30605489 http://dx.doi.org/10.1371/journal.pone.0210004 Text en © 2019 Pechmann et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pechmann, Astrid
Wellmann, Sven
Stoecklin, Benjamin
Krüger, Marcus
Zieger, Barbara
Increased von Willebrand factor parameters in children with febrile seizures
title Increased von Willebrand factor parameters in children with febrile seizures
title_full Increased von Willebrand factor parameters in children with febrile seizures
title_fullStr Increased von Willebrand factor parameters in children with febrile seizures
title_full_unstemmed Increased von Willebrand factor parameters in children with febrile seizures
title_short Increased von Willebrand factor parameters in children with febrile seizures
title_sort increased von willebrand factor parameters in children with febrile seizures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317815/
https://www.ncbi.nlm.nih.gov/pubmed/30605489
http://dx.doi.org/10.1371/journal.pone.0210004
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