Evidence map›Paper›PMID 35190890›Full record

ArticleJournal of neurology2022

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

Aurélie Hanin, Jérôme Alexandre Denis, Valerio Frazzini, Louis Cousyn, Françoise Imbert-Bismut, Benoit Rucheton, Dominique Bonnefont-Rousselot, Clémence Marois, Virginie Lambrecq, Sophie Demeret and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
6.1field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Observational
  6. The Role of GDNF and NSE in Attention-deficit/Hyperactivity Disorder: The Relationship with Sleep and Eating.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2026
    Article
  7. Pathophysiology of Status Epilepticus Revisited.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Review
  10. Circulating microRNAs as Biomarkers of Various Forms of Epilepsy.Medical sciences (Basel, Switzerland) · 2025
    Article
  11. Review
  12. Article
  13. Observational
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
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  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Aurélie HaninSorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.ORCID http://orcid.org/0000-0002-5912-9998
Jérôme Alexandre DenisSorbonne Université, Paris, France.ORCID http://orcid.org/0000-0002-1617-4617
Valerio FrazziniSorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.ORCID http://orcid.org/0000-0003-1187-3352
Louis CousynSorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.ORCID http://orcid.org/0000-0003-1407-5575
Françoise Imbert-BismutAP-HP, Metabolic Biochemistry Department, Pitié-Salpêtrière Hospital, Paris, France.
Benoit RuchetonAP-HP, Metabolic Biochemistry Department, Pitié-Salpêtrière Hospital, Paris, France.ORCID http://orcid.org/0000-0002-5893-6595
Dominique Bonnefont-RousselotAP-HP, Metabolic Biochemistry Department, Pitié-Salpêtrière Hospital, Paris, France.ORCID http://orcid.org/0000-0003-4689-9202
Clémence MaroisAP-HP, Neuro-Intensive Care Unit, Pitié-Salpêtrière Hospital, Paris, France.ORCID http://orcid.org/0000-0002-3266-0623
Virginie LambrecqSorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.ORCID http://orcid.org/0000-0001-9442-0302
Sophie DemeretAP-HP, Neuro-Intensive Care Unit, Pitié-Salpêtrière Hospital, Paris, France.ORCID http://orcid.org/0000-0002-0523-6472
Vincent NavarroSorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France. vincent.navarro@aphp.fr.ORCID http://orcid.org/0000-0003-0077-8114
Centre National de la Recherche Scientifique · FRSorbonne Université · FR

Funding

Agence Nationale de la Recherche ANR-10-IAIHU-06Fondation Assitance Publique-Hôpitaux de Paris EPIRES- Marie Laure PLV MerchandisingFondation Recherche Médicale FDM20170839111
6 · The paper itself

Abstract

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.

Indexed as

EpilepsyStatus EpilepticusBiomarkersHumansPhosphopyruvate HydrataseProgranulinsS100 Calcium Binding Protein beta SubunitBiomarkersPhosphopyruvate HydrataseProgranulinsS100B protein, humanS100 Calcium Binding Protein beta SubunitDiagnosisEtiologyNeuron Specific EnolaseProgranulinS100-beta proteinStatus epilepticus

Identifiers

PMID35190890
OpenAlexW4212782998

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.