Copeptin as a serum biomarker of febrile seizures.

Accurate diagnosis of febrile seizures in children presenting after paroxysmal episodes associated with fever, is hampered by the lack of objective postictal biomarkers. The aim of our study was to investigate whether FS are associated with increased levels of serum copeptin, a robust marker of argi...

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Main Authors: Benjamin Stöcklin, Sotirios Fouzas, Paula Schillinger, Sevgi Cayir, Roswitha Skendaj, Michel Ramser, Peter Weber, Sven Wellmann
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4404343?pdf=render
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spelling doaj-b1add3181341434aae14489419c05cc62020-11-24T22:03:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01104e012466310.1371/journal.pone.0124663Copeptin as a serum biomarker of febrile seizures.Benjamin StöcklinSotirios FouzasPaula SchillingerSevgi CayirRoswitha SkendajMichel RamserPeter WeberSven WellmannAccurate diagnosis of febrile seizures in children presenting after paroxysmal episodes associated with fever, is hampered by the lack of objective postictal biomarkers. The aim of our study was to investigate whether FS are associated with increased levels of serum copeptin, a robust marker of arginine vasopressin secretion.This was a prospective emergency-setting cross-sectional study of 161 children between six months and five years of age. Of these, 83 were diagnosed with febrile seizures, 69 had a febrile infection without seizures and nine had epileptic seizures not triggered by infection. Serum copeptin and prolactin levels were measured in addition to standard clinical, neurophysiological, and laboratory assessment.NCT01884766.Circulating copeptin was significantly higher in children with febrile seizures (median [interquartile range] 18.9 pmol/L [8.5-36.6]) compared to febrile controls (5.6 pmol/L [4.1-9.4]; p < 0.001), with no differences between febrile and epileptic seizures (21.4 pmol/L [16.1-46.6]; p = 0.728). In a multivariable regression model, seizures were the major determinant of serum copeptin (beta 0.509; p < 0.001), independently of clinical and baseline laboratory indices. The area under the receiver operating curve for copeptin was 0.824 (95% CI 0.753-0.881), significantly higher compared to prolactin (0.667 [0.585-0.742]; p < 0.001). The diagnostic accuracy of copeptin increased with decreasing time elapsed since the convulsive event (at 120 min: 0.879 [0.806-0.932] and at <60 min: 0.975 [0.913-0.997]).Circulating copeptin has high diagnostic accuracy in febrile seizures and may be a useful adjunct for accurately diagnosing postictal states in the emergency setting.http://europepmc.org/articles/PMC4404343?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Benjamin Stöcklin
Sotirios Fouzas
Paula Schillinger
Sevgi Cayir
Roswitha Skendaj
Michel Ramser
Peter Weber
Sven Wellmann
spellingShingle Benjamin Stöcklin
Sotirios Fouzas
Paula Schillinger
Sevgi Cayir
Roswitha Skendaj
Michel Ramser
Peter Weber
Sven Wellmann
Copeptin as a serum biomarker of febrile seizures.
PLoS ONE
author_facet Benjamin Stöcklin
Sotirios Fouzas
Paula Schillinger
Sevgi Cayir
Roswitha Skendaj
Michel Ramser
Peter Weber
Sven Wellmann
author_sort Benjamin Stöcklin
title Copeptin as a serum biomarker of febrile seizures.
title_short Copeptin as a serum biomarker of febrile seizures.
title_full Copeptin as a serum biomarker of febrile seizures.
title_fullStr Copeptin as a serum biomarker of febrile seizures.
title_full_unstemmed Copeptin as a serum biomarker of febrile seizures.
title_sort copeptin as a serum biomarker of febrile seizures.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Accurate diagnosis of febrile seizures in children presenting after paroxysmal episodes associated with fever, is hampered by the lack of objective postictal biomarkers. The aim of our study was to investigate whether FS are associated with increased levels of serum copeptin, a robust marker of arginine vasopressin secretion.This was a prospective emergency-setting cross-sectional study of 161 children between six months and five years of age. Of these, 83 were diagnosed with febrile seizures, 69 had a febrile infection without seizures and nine had epileptic seizures not triggered by infection. Serum copeptin and prolactin levels were measured in addition to standard clinical, neurophysiological, and laboratory assessment.NCT01884766.Circulating copeptin was significantly higher in children with febrile seizures (median [interquartile range] 18.9 pmol/L [8.5-36.6]) compared to febrile controls (5.6 pmol/L [4.1-9.4]; p < 0.001), with no differences between febrile and epileptic seizures (21.4 pmol/L [16.1-46.6]; p = 0.728). In a multivariable regression model, seizures were the major determinant of serum copeptin (beta 0.509; p < 0.001), independently of clinical and baseline laboratory indices. The area under the receiver operating curve for copeptin was 0.824 (95% CI 0.753-0.881), significantly higher compared to prolactin (0.667 [0.585-0.742]; p < 0.001). The diagnostic accuracy of copeptin increased with decreasing time elapsed since the convulsive event (at 120 min: 0.879 [0.806-0.932] and at <60 min: 0.975 [0.913-0.997]).Circulating copeptin has high diagnostic accuracy in febrile seizures and may be a useful adjunct for accurately diagnosing postictal states in the emergency setting.
url http://europepmc.org/articles/PMC4404343?pdf=render
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