Evidence map›Paper›PMID 41002933›Full record

ArticleNeurology international2025

Biological Plausibility of Using Plasma Amino Acid Profile Determination as a Potential Biomarker for Pediatric Patients with Mild Traumatic Brain Injuries.

Adán Pérez-Arredondo, Eduardo Cázares-Ramírez, Luis Tristán-López, Carlos Jiménez-Gutiérrez, Diana L Pérez-Lozano, Ivette A Martínez-Hernández, Valentina Vega-Rangel, Hugo F Narváez-González, Camilo Rios, Marina Martínez-Vargas and 2 more

Abstract read
In one paragraph

Article in Neurology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Adán Pérez-ArredondoDepartamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.ORCID 0000-0002-0479-6734
Eduardo Cázares-RamírezDepartamento de Urgencias Médicas Pediátricas, Instituto Nacional de Pediatría, Mexico City 04530, Mexico.ORCID 0000-0002-0918-3910
Luis Tristán-LópezLaboratorio de Neuroquímica, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Mexico City 14269, Mexico.ORCID 0000-0002-8033-0629
Carlos Jiménez-GutiérrezPrograma de Maestría y Doctorado en Ciencias Médicas, Odontológicas y de la Salud, Investigación Clínica Experimental, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.ORCID 0000-0003-1108-2139
Diana L Pérez-LozanoCoordinación de Medicina General y Comunitaria, Universidad de la Salud, Campus Santa Fe, Mexico City 01210, Mexico.
Ivette A Martínez-HernándezHospital "Primero de Octubre", Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado (ISSSTE), Mexico City 73000, Mexico.
Valentina Vega-RangelDepartamento de Urgencias Médicas Pediátricas, Instituto Nacional de Pediatría, Mexico City 04530, Mexico.
Hugo F Narváez-GonzálezCentro Médico Nacional "20 de Noviembre", Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado (ISSSTE), Mexico City 03100, Mexico.ORCID 0000-0001-7229-4675
Camilo RiosInstituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.
Marina Martínez-VargasDepartamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.
Luz NavarroDepartamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.ORCID 0000-0002-5519-0871
Liliana Carmona-AparicioPrograma de Maestría y Doctorado en Ciencias Médicas, Odontológicas y de la Salud, Investigación Clínica Experimental, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.

Funding

DGAPA PAPIIT IN228223Instituto Nacional de Pediatria Protocol 030/2015 (Program E-022)SECIHTI No. 261721
6 · The paper itself

Abstract

backgroundAmino acid biomarkers have a crucial influence on our understanding of brain injury mechanisms, and their plasma concentrations may indicate neurological damage and recovery patterns. Pediatric mild traumatic brain injury (mTBI) assessment particularly benefits from such molecular indicators, as clinical presentations can be subtle and variable. However, current diagnostic and prognostic tools lack reliable biochemical markers that can track the temporal evolution of injuries and recovery.

methodsWe conducted a prospective longitudinal cohort study involving 36 pediatric mTBI patients and 44 controls to characterize the temporal evolution of key amino acids and their derived indices. Blood samples were collected at 3, 6, 12, and 24 h and at 7, 14, and 28 days post-injury, with amino acids quantified using high-performance liquid chromatography.

resultsOur analysis revealed significant temporal changes in glutamate, glutamine, and glycine concentrations, with glutamate peaking at day 7 before declining, while glutamine showed steady increases throughout. The GLN/GLU ratio demonstrated an early excitatory imbalance followed by astrocytic compensation, and the GLX ratio indicated progressive recovery.

conclusionsThese patterns represent continuous neurochemical processes involving excitotoxicity and glial regulation, suggesting potential utility as biomarkers for mTBI diagnosis and monitoring. While further validation using larger cohorts is needed, these findings provide compelling evidence of the efficacy of using amino acid profiles to track pediatric mTBI progression and recovery.

Indexed as

amino acidsaspartateglutamateglutamineglycinemild traumatic brain injurypediatric

Identifiers

PMID41002933
PMCPMC12473026

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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.