Neuron Specific Enolase, S100-beta protein and progranulin as diagnostic biomarkers of status epilepticus.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 01 12 2021
accepted: 30 01 2022
revised: 29 01 2022
pubmed: 23 2 2022
medline: 25 6 2022
entrez: 22 2 2022
Statut: ppublish

Résumé

Status epilepticus (SE) is a life-threatening prolonged epileptic seizure. A rapid diagnosis is fundamental to initiate antiepileptic treatment and to prevent the development of neurological sequels. Several serum and cerebrospinal fluid biomarkers have been proposed to help in the diagnosis of SE. Nevertheless, previous studies were conducted on too small patient cohorts, precluding the utilization of interesting biomarkers for the SE diagnosis. Here, we aimed to assess the ability of Neuron Specific Enolase (NSE), S100-beta protein (S100B) and progranulin to help in the diagnosis of SE in a large cohort of patients (36 control patients, 56 patients with pharmacoresistant epilepsy and 82 SE patients). Blood NSE, S100B and progranulin levels were higher in SE patients when compared with control patients or patients with pharmacoresistant epilepsy. Both NSE and progranulin levels were higher in cerebrospinal fluid from SE patients when compared with control patients. The receiver-operating characteristics curves revealed good accuracy at detecting SE for serum S100B (AUC 0.748) and plasma progranulin (AUC 0.756). The performances were lower for serum NSE (AUC 0.624). Eighty-four percent of patients with serum S100B levels above 0.09 ng/mL presented with a SE, whereas 90% of patients without SE had serum S100B levels lower than 0.09 ng/mL. Serum S100B levels were not significantly different according to SE etiology, SE semiology or SE refractoriness. Our results confirm that NSE, S100B and progranulin levels are increased after SE. We suggest that serum S100B levels might be added to clinical evaluation and electroencephalogram to identify difficult-to-diagnose form of SE.

Identifiants

pubmed: 35190890
doi: 10.1007/s00415-022-11004-2
pii: 10.1007/s00415-022-11004-2
doi:

Substances chimiques

Biomarkers 0
Progranulins 0
S100 Calcium Binding Protein beta Subunit 0
S100B protein, human 0
Phosphopyruvate Hydratase EC 4.2.1.11

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3752-3760

Subventions

Organisme : Agence Nationale de la Recherche
ID : ANR-10-IAIHU-06
Organisme : Fondation Recherche Médicale
ID : FDM20170839111
Organisme : Fondation Assitance Publique-Hôpitaux de Paris
ID : EPIRES- Marie Laure PLV Merchandising

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

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Auteurs

Aurélie Hanin (A)

Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
AP-HP, Epilepsy Unit and Clinical Neurophysiology Department, DMU Neurosciences, Pitié-Salpêtrière Hospital, Paris, France.

Jérôme Alexandre Denis (JA)

Sorbonne Université, Paris, France.
AP-HP, Endocrine and Oncological Biochemistry Department, Pitié-Salpêtrière Hospital, Paris, France.

Valerio Frazzini (V)

Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
AP-HP, Epilepsy Unit and Clinical Neurophysiology Department, DMU Neurosciences, Pitié-Salpêtrière Hospital, Paris, France.

Louis Cousyn (L)

Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
AP-HP, Epilepsy Unit and Clinical Neurophysiology Department, DMU Neurosciences, Pitié-Salpêtrière Hospital, Paris, France.

Françoise Imbert-Bismut (F)

AP-HP, Metabolic Biochemistry Department, Pitié-Salpêtrière Hospital, Paris, France.

Benoit Rucheton (B)

AP-HP, Metabolic Biochemistry Department, Pitié-Salpêtrière Hospital, Paris, France.

Dominique Bonnefont-Rousselot (D)

AP-HP, Metabolic Biochemistry Department, Pitié-Salpêtrière Hospital, Paris, France.
UTCBS, CNRS, INSERM, Université de Paris, Paris, France.

Clémence Marois (C)

AP-HP, Neuro-Intensive Care Unit, Pitié-Salpêtrière Hospital, Paris, France.

Virginie Lambrecq (V)

Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
AP-HP, Epilepsy Unit and Clinical Neurophysiology Department, DMU Neurosciences, Pitié-Salpêtrière Hospital, Paris, France.
Sorbonne Université, Paris, France.

Sophie Demeret (S)

AP-HP, Neuro-Intensive Care Unit, Pitié-Salpêtrière Hospital, Paris, France.

Vincent Navarro (V)

Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France. vincent.navarro@aphp.fr.
AP-HP, Epilepsy Unit and Clinical Neurophysiology Department, DMU Neurosciences, Pitié-Salpêtrière Hospital, Paris, France. vincent.navarro@aphp.fr.
Sorbonne Université, Paris, France. vincent.navarro@aphp.fr.
AP-HP, Center of Reference for Rare Epilepsies, Pitié-Salpêtrière Hospital, Paris, France. vincent.navarro@aphp.fr.

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