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Metabonomic analysis of cerebrospinal fluid in epilepsy

BACKGROUND: We sought to explore the relationship between epilepsy and cerebrospinal fluid metabolomics and identify biomarkers for the diagnosis, treatment, and prognosis of epilepsy. METHODS: In total, 23 epileptic patients treated at The First Affiliated Hospital of Dalian Medical University from...

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Autores principales: Niu, Di, Sun, Pin, Zhang, Fenghua, Song, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096421/
https://www.ncbi.nlm.nih.gov/pubmed/35571432
http://dx.doi.org/10.21037/atm-22-1219
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author Niu, Di
Sun, Pin
Zhang, Fenghua
Song, Fan
author_facet Niu, Di
Sun, Pin
Zhang, Fenghua
Song, Fan
author_sort Niu, Di
collection PubMed
description BACKGROUND: We sought to explore the relationship between epilepsy and cerebrospinal fluid metabolomics and identify biomarkers for the diagnosis, treatment, and prognosis of epilepsy. METHODS: In total, 23 epileptic patients treated at The First Affiliated Hospital of Dalian Medical University from April 2019 to September 2019 were selected for the disease group and 13 non-epileptic patients were selected for the control group. Cerebrospinal fluid samples were collected from both groups, and the metabolites were analyzed by gas chromatography–mass spectrometry. The metabolites differentially expressed in the cerebrospinal fluid samples were identified. A differential metabolite enrichment analysis was performed to determine the metabolic pathways. RESULTS: Using a variable importance in the projection value >1 and a P value <0.05 as the screening criteria, we found that 3 metabolites (i.e., alpha-ketoisocaproic acid 1, xylose 1, and glycine 2) were differentially expressed in the cerebrospinal fluid of the 23 epileptic patients compared to the 13 non-epileptic patients. Alpha-ketoisocaproic acid 1 and xylose 1 were highly expressed in the epileptic cerebrospinal fluid samples, while glycine 2 was lowly expressed in the epileptic cerebrospinal fluid samples. Additionally, the 3 metabolites were significantly enriched in the 5 metabolic pathways of primary bile acid biosynthesis, valine, leucine, and isoleucine degradation, glutathione metabolism, glyoxylate and dicarboxylate metabolism, and glycine, serine, and threonine metabolism. CONCLUSIONS: The present study examined the metabolites of the cerebrospinal fluid of epileptic patients and non-epileptic patients. Our findings provide insights that may inform the discovery of therapeutic targets and diagnostic markers for epilepsy.
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spelling pubmed-90964212022-05-13 Metabonomic analysis of cerebrospinal fluid in epilepsy Niu, Di Sun, Pin Zhang, Fenghua Song, Fan Ann Transl Med Original Article BACKGROUND: We sought to explore the relationship between epilepsy and cerebrospinal fluid metabolomics and identify biomarkers for the diagnosis, treatment, and prognosis of epilepsy. METHODS: In total, 23 epileptic patients treated at The First Affiliated Hospital of Dalian Medical University from April 2019 to September 2019 were selected for the disease group and 13 non-epileptic patients were selected for the control group. Cerebrospinal fluid samples were collected from both groups, and the metabolites were analyzed by gas chromatography–mass spectrometry. The metabolites differentially expressed in the cerebrospinal fluid samples were identified. A differential metabolite enrichment analysis was performed to determine the metabolic pathways. RESULTS: Using a variable importance in the projection value >1 and a P value <0.05 as the screening criteria, we found that 3 metabolites (i.e., alpha-ketoisocaproic acid 1, xylose 1, and glycine 2) were differentially expressed in the cerebrospinal fluid of the 23 epileptic patients compared to the 13 non-epileptic patients. Alpha-ketoisocaproic acid 1 and xylose 1 were highly expressed in the epileptic cerebrospinal fluid samples, while glycine 2 was lowly expressed in the epileptic cerebrospinal fluid samples. Additionally, the 3 metabolites were significantly enriched in the 5 metabolic pathways of primary bile acid biosynthesis, valine, leucine, and isoleucine degradation, glutathione metabolism, glyoxylate and dicarboxylate metabolism, and glycine, serine, and threonine metabolism. CONCLUSIONS: The present study examined the metabolites of the cerebrospinal fluid of epileptic patients and non-epileptic patients. Our findings provide insights that may inform the discovery of therapeutic targets and diagnostic markers for epilepsy. AME Publishing Company 2022-04 /pmc/articles/PMC9096421/ /pubmed/35571432 http://dx.doi.org/10.21037/atm-22-1219 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Niu, Di
Sun, Pin
Zhang, Fenghua
Song, Fan
Metabonomic analysis of cerebrospinal fluid in epilepsy
title Metabonomic analysis of cerebrospinal fluid in epilepsy
title_full Metabonomic analysis of cerebrospinal fluid in epilepsy
title_fullStr Metabonomic analysis of cerebrospinal fluid in epilepsy
title_full_unstemmed Metabonomic analysis of cerebrospinal fluid in epilepsy
title_short Metabonomic analysis of cerebrospinal fluid in epilepsy
title_sort metabonomic analysis of cerebrospinal fluid in epilepsy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096421/
https://www.ncbi.nlm.nih.gov/pubmed/35571432
http://dx.doi.org/10.21037/atm-22-1219
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