Neuron-specific enolase is correlated with lesion topology, relative infarct volume and outcome of symptomatic NAIS.


Journal

Archives of disease in childhood. Fetal and neonatal edition
ISSN: 1468-2052
Titre abrégé: Arch Dis Child Fetal Neonatal Ed
Pays: England
ID NLM: 9501297

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 11 12 2018
revised: 27 03 2019
accepted: 12 05 2019
pubmed: 16 6 2019
medline: 10 3 2020
entrez: 16 6 2019
Statut: ppublish

Résumé

To correlate neuron-specific enolase (NSE) levels in cerebrospinal fluid (CSF) in neonate infants with symptomatic neonatal arterial ischaemic stroke (NAIS) with the arterial distribution of infarct, infarct volume and outcome. Prospective observational multicentre cohort. Three paediatric university hospitals in Spain. Thirty-eight neonates with more than 35 weeks' gestational age between 2006 and 2016 were studied. They were diagnosed with NAIS by MRI. They underwent a lumbar puncture to measure CSF-NSE concentrations within 96 hours after the onset of symptoms. Sixty-seven neonates admitted with suspected infections served as controls. We used a classification based on the arterial distribution, and the lesions were segmented with ITK-Snap software to determine their volume. Neurodevelopment was assessed at 24 months using the Bayley-III, Gross Motor Function Classification System and Bimanual Fine Motor Function. CSF-NSE levels were higher in patients with symptomatic NAIS when compared with controls. Neonates with multifocal NAIS and with NAIS located in middle cerebral artery (MCA)-M1 arterial territory showed higher CSF-NSE levels when compared with cases with MCA-M2-M3-M4 territories (p<0.001). A significant correlation was found between CSF-NSE and relative infarction volume (r CSF-NSE is a potential early prognostic biomarker after an NAIS due to the relation between volume, topology and neurodevelopment at 2 years of age.

Identifiants

pubmed: 31201253
pii: archdischild-2018-316680
doi: 10.1136/archdischild-2018-316680
doi:

Substances chimiques

Biomarkers 0
Phosphopyruvate Hydratase EC 4.2.1.11

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

132-137

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Gemma Arca (G)

Department of Neonatology, Clinic Maternitat University Hospital, Barcelona, Spain.
Fundación NeNe, Madrid, Spain.

Juan Arnaez (J)

Fundación NeNe, Madrid, Spain.
Department of Neonatology, Burgos University Hospital, Burgos, Spain.

Thais Agut (T)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Department of Neonatology, Hospital Sant Joan de Déu, Barcelona, Spain.

Christian Núñez (C)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Parc Sanitari Sant Joan de Déu, Sant Boi de Llobregat, Barcelona, Spain.

Christian Stephan-Otto (C)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Parc Sanitari Sant Joan de Déu, Sant Boi de Llobregat, Barcelona, Spain.
Centro de Investigación Biomédica en Red de Salud Mental, Madrid, Spain.

Anna Valls (A)

Hospital Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.

Alfredo García-Alix (A)

Fundación NeNe, Madrid, Spain.
Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.

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