Cargando…

Preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder

BACKGROUND: Autism spectrum disorder (ASD) is a complex group of heterogeneous neurodevelopmental disorders the prevalence of which has been in the rise in the past decade. In an attempt to better target the basic causes of ASD for diagnosis and treatment, efforts to identify reliable biomarkers rel...

Descripción completa

Detalles Bibliográficos
Autores principales: El-Ansary, Afaf, Hassan, Wail M., Daghestani, Maha, Al-Ayadhi, Laila, Ben Bacha, Abir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964874/
https://www.ncbi.nlm.nih.gov/pubmed/31945130
http://dx.doi.org/10.1371/journal.pone.0227626
_version_ 1783488539308064768
author El-Ansary, Afaf
Hassan, Wail M.
Daghestani, Maha
Al-Ayadhi, Laila
Ben Bacha, Abir
author_facet El-Ansary, Afaf
Hassan, Wail M.
Daghestani, Maha
Al-Ayadhi, Laila
Ben Bacha, Abir
author_sort El-Ansary, Afaf
collection PubMed
description BACKGROUND: Autism spectrum disorder (ASD) is a complex group of heterogeneous neurodevelopmental disorders the prevalence of which has been in the rise in the past decade. In an attempt to better target the basic causes of ASD for diagnosis and treatment, efforts to identify reliable biomarkers related to the body’s metabolism are increasing. Despite an increase in identifying biomarkers in ASD, there are none so far with enough evidence to be used in routine clinical examination, unless medical illness is suspected. Promising biomarkers include those of mitochondrial dysfunction, oxidative stress, energy metabolism, and apoptosis. METHODS AND PARTICIPANTS: Sodium (Na+), Potassium (K+), glutathione (GSH), glutathione-s-transferase (GST), Creatine kinase (CK), lactate dehydrogenase (LDH), Coenzyme Q10, and melatonin (MLTN) were evaluated in 13 participants with ASD and 24 age-matched healthy controls. Additionally, five ratios, which include Na(+)/K(+), GSH:GST, CK:Cas7, CoQ10: Cas 7, and Cas7:MLTN, were tested to measure their predictive values in discriminating between autistic individuals and controls. These markers, either in absolute values, as five ratios, or combined (9 markers + 5 ratios) were subjected to a principal component analysis and multidimensional scaling (MDS), and hierarchical clustering, which are helpful statistical tools in the field of biomarkers. RESULTS: Our data demonstrated that both PCA and MDS analysis were effective in separating autistic from control subjects completely. This was also confirmed through the use of hierarchical clustering, which showed complete separation of the autistic and control groups based on nine biomarkers, five biomarker ratios, or a combined profile. Excellent predictive value of the measured profile was obtained using the receiver operating characteristics analysis, which showed an area under the curve of 1. CONCLUSION: The availability of an improved predictive profile, represented by nine biomarkers plus the five ratios, inter-related different etiological mechanisms in ASD and would be valuable in providing greater recognition of the altered biological pathways in ASD. Our predictive profile could be used for the diagnosis and intervention of ASD.
format Online
Article
Text
id pubmed-6964874
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-69648742020-01-26 Preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder El-Ansary, Afaf Hassan, Wail M. Daghestani, Maha Al-Ayadhi, Laila Ben Bacha, Abir PLoS One Research Article BACKGROUND: Autism spectrum disorder (ASD) is a complex group of heterogeneous neurodevelopmental disorders the prevalence of which has been in the rise in the past decade. In an attempt to better target the basic causes of ASD for diagnosis and treatment, efforts to identify reliable biomarkers related to the body’s metabolism are increasing. Despite an increase in identifying biomarkers in ASD, there are none so far with enough evidence to be used in routine clinical examination, unless medical illness is suspected. Promising biomarkers include those of mitochondrial dysfunction, oxidative stress, energy metabolism, and apoptosis. METHODS AND PARTICIPANTS: Sodium (Na+), Potassium (K+), glutathione (GSH), glutathione-s-transferase (GST), Creatine kinase (CK), lactate dehydrogenase (LDH), Coenzyme Q10, and melatonin (MLTN) were evaluated in 13 participants with ASD and 24 age-matched healthy controls. Additionally, five ratios, which include Na(+)/K(+), GSH:GST, CK:Cas7, CoQ10: Cas 7, and Cas7:MLTN, were tested to measure their predictive values in discriminating between autistic individuals and controls. These markers, either in absolute values, as five ratios, or combined (9 markers + 5 ratios) were subjected to a principal component analysis and multidimensional scaling (MDS), and hierarchical clustering, which are helpful statistical tools in the field of biomarkers. RESULTS: Our data demonstrated that both PCA and MDS analysis were effective in separating autistic from control subjects completely. This was also confirmed through the use of hierarchical clustering, which showed complete separation of the autistic and control groups based on nine biomarkers, five biomarker ratios, or a combined profile. Excellent predictive value of the measured profile was obtained using the receiver operating characteristics analysis, which showed an area under the curve of 1. CONCLUSION: The availability of an improved predictive profile, represented by nine biomarkers plus the five ratios, inter-related different etiological mechanisms in ASD and would be valuable in providing greater recognition of the altered biological pathways in ASD. Our predictive profile could be used for the diagnosis and intervention of ASD. Public Library of Science 2020-01-16 /pmc/articles/PMC6964874/ /pubmed/31945130 http://dx.doi.org/10.1371/journal.pone.0227626 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
El-Ansary, Afaf
Hassan, Wail M.
Daghestani, Maha
Al-Ayadhi, Laila
Ben Bacha, Abir
Preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder
title Preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder
title_full Preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder
title_fullStr Preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder
title_full_unstemmed Preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder
title_short Preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder
title_sort preliminary evaluation of a novel nine-biomarker profile for the prediction of autism spectrum disorder
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964874/
https://www.ncbi.nlm.nih.gov/pubmed/31945130
http://dx.doi.org/10.1371/journal.pone.0227626
work_keys_str_mv AT elansaryafaf preliminaryevaluationofanovelninebiomarkerprofileforthepredictionofautismspectrumdisorder
AT hassanwailm preliminaryevaluationofanovelninebiomarkerprofileforthepredictionofautismspectrumdisorder
AT daghestanimaha preliminaryevaluationofanovelninebiomarkerprofileforthepredictionofautismspectrumdisorder
AT alayadhilaila preliminaryevaluationofanovelninebiomarkerprofileforthepredictionofautismspectrumdisorder
AT benbachaabir preliminaryevaluationofanovelninebiomarkerprofileforthepredictionofautismspectrumdisorder