Cerebrospinal fluid neopterin as a biomarker of neuroinflammatory diseases.

The elevation of neopterin in cerebrospinal fuid (CSF) has been reported in several neuroinfammatory disorders. However, it is not expected that neopterin alone can discriminate among diferent neuroinfammatory etiologies. We conducted an observational retrospective and case-control study to analyze...

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Detalles Bibliográficos
Autores: Molero Luis, Marta, Casas Alba, Dídac, Orellana, Gabriela, Ormazabal Herrero, Aida, Sierra, Cristina, Oliva, Clara, Valls, Anna, Velasco, Jesus, Launes Montaña, Cristian, Cuadras, Daniel, Pérez Dueñas, Belén, Jordán García, Iolanda, Cambra Lasaosa, Francisco José, Ortigoza Escobar, Juan D., Muñoz Almagro, Carmen, Garcia-Cazorla, Àngels, Armangué, Thaís, Artuch Iriberri, Rafael
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/186686
Acceso en línea:https://hdl.handle.net/2445/186686
Access Level:acceso abierto
Palabra clave:Líquid cefalorraquidi
Neopterina
Virologia
Cromatografia
Cerebrospinal fluid
Neopterin
Virology
Chromatography
Descripción
Sumario:The elevation of neopterin in cerebrospinal fuid (CSF) has been reported in several neuroinfammatory disorders. However, it is not expected that neopterin alone can discriminate among diferent neuroinfammatory etiologies. We conducted an observational retrospective and case-control study to analyze the CSF biomarkers neopterin, total proteins, and leukocytes in a large cohort of pediatric patients with neuroinfammatory disorders. CSF samples from 277 subjects were included and classifed into four groups: Viral meningoencephalitis, bacterial meningitis, acquired immunemediated disorders, and patients with no-immune diseases (control group). CSF neopterin was analyzed with high-performance liquid chromatography. Microbiological diagnosis included bacterial CSF cultures and several specifc real-time polymerase chain reactions. Molecular testing for multiple respiratory pathogens was also included. Antibodies against neuronal and glial proteins were tested. Canonical discriminant analysis of the three biomarkers was conducted to establish the best discriminant functions for the classifcation of the diferent clinical groups. Model validation was done by biomarker analyses in a new cohort of 95 pediatric patients. CSF neopterin displayed the highest values in the viral and bacterial infection groups. By applying canonical discriminant analysis, it was possible to classify the patients into the diferent groups. Validation analyses displayed good results for neuropediatric patients with no-immune diseases and for viral meningitis patients, followed by the other groups. This study provides initial evidence of a more efcient approach to promote the timely classifcation of patients with viral and bacterial infections and acquired autoimmune disorders. Through canonical equations, we have validated a new tool that aids in the early and diferential diagnosis of these neuroinfammatory conditions.