A Novel UHPLC-MS Method Targeting Urinary Metabolomic Markers for Autism Spectrum Disorder.

autism spectrum disorder gut microbiota liquid chromatography mass spectrometry metabolomics oxidative stress

Journal

Metabolites
ISSN: 2218-1989
Titre abrégé: Metabolites
Pays: Switzerland
ID NLM: 101578790

Informations de publication

Date de publication:
02 Nov 2020
Historique:
received: 14 09 2020
revised: 20 10 2020
accepted: 29 10 2020
entrez: 5 11 2020
pubmed: 6 11 2020
medline: 6 11 2020
Statut: epublish

Résumé

Autism spectrum disorder is a heterogeneous neurodevelopmental disease. Currently, no biomarker of this disease is known. Diagnosis is performed through observation, standardized behavioral scales, and interviews with parents. In practice, diagnosis is often delayed to the average age of four years or even more which adversely affects a child's perspective. A laboratory method allowing to detect the disorder at earlier stages is of a great need, as this could help the patients to start with treatment at a younger age, even prior to the clinical diagnosis. Recent evidence indicates that metabolomic markers should be considered as diagnostic markers, also serving for further differentiation and characterization of different subgroups of the autism spectrum. In this study, we developed an ultra-high performance liquid chromatography-tandem triple quadrupole mass spectrometry method for the simultaneous determination of six metabolites in human urine. These metabolites, namely methylguanidine, N-acetyl arginine, inosine, indole-3-acetic acid, indoxyl sulfate and xanthurenic acid were selected as potential biomarkers according to prior metabolomic studies. The analysis was carried out by means of reversed-phase liquid chromatography with gradient elution. Separation of the metabolites was performed on a Phenomenex Luna

Identifiants

pubmed: 33147863
pii: metabo10110443
doi: 10.3390/metabo10110443
pmc: PMC7693535
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Agentúra na Podporu Výskumu a Vývoja
ID : 15-0045
Organisme : Agentúra na Podporu Výskumu a Vývoja
ID : 15-0085
Organisme : Ministerstvo skolstva SR
ID : 2/0088/18
Organisme : Ministrerstvo zdravotnictva SR
ID : 2018/24-SAV-2
Organisme : International Centre for Genetic Engineering and Biotechnology
ID : CRP/19/016

Déclaration de conflit d'intérêts

The authors declare no conflict of interest

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Auteurs

Dominika Olesova (D)

Institute of Neuroimmunology, Slovak Academy of Sciences, Dubravska cesta 9, 84510 Bratislava, Slovakia.

Jaroslav Galba (J)

Department of Pharmaceutical Analysis and Nuclear Pharmacy, Faculty of Pharmacy, Comenius University in Bratislava, Odbojarov 10, 832 32 Bratislava, Slovakia.

Juraj Piestansky (J)

Department of Pharmaceutical Analysis and Nuclear Pharmacy, Faculty of Pharmacy, Comenius University in Bratislava, Odbojarov 10, 832 32 Bratislava, Slovakia.

Hana Celusakova (H)

Institute of Physiology, Faculty of Medicine, Comenius University in Bratislava, Sasinkova 2, 813 72 Bratislava, Slovakia.

Gabriela Repiska (G)

Institute of Physiology, Faculty of Medicine, Comenius University in Bratislava, Sasinkova 2, 813 72 Bratislava, Slovakia.

Katarina Babinska (K)

Institute of Physiology, Faculty of Medicine, Comenius University in Bratislava, Sasinkova 2, 813 72 Bratislava, Slovakia.

Daniela Ostatnikova (D)

Institute of Physiology, Faculty of Medicine, Comenius University in Bratislava, Sasinkova 2, 813 72 Bratislava, Slovakia.

Stanislav Katina (S)

Institute of Mathematics and Statistics, Faculty of Science, Masaryk University, Kotlářská 267/2, 611 37 Brno, Czech Republic.

Andrej Kovac (A)

Institute of Neuroimmunology, Slovak Academy of Sciences, Dubravska cesta 9, 84510 Bratislava, Slovakia.

Classifications MeSH