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Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes

BACKGROUND: Numerous studies have highlighted the elevated degree of comorbidity associated with autism spectrum disorder (ASD). These comorbid conditions may add further impairments to individuals with autism and are substantially more prevalent compared to neurotypical populations. These high rate...

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Autores principales: Diaz-Beltran, Leticia, Esteban, Francisco J., Varma, Maya, Ortuzk, Alp, David, Maude, Wall, Dennis P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399393/
https://www.ncbi.nlm.nih.gov/pubmed/28427329
http://dx.doi.org/10.1186/s12864-017-3667-9
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author Diaz-Beltran, Leticia
Esteban, Francisco J.
Varma, Maya
Ortuzk, Alp
David, Maude
Wall, Dennis P.
author_facet Diaz-Beltran, Leticia
Esteban, Francisco J.
Varma, Maya
Ortuzk, Alp
David, Maude
Wall, Dennis P.
author_sort Diaz-Beltran, Leticia
collection PubMed
description BACKGROUND: Numerous studies have highlighted the elevated degree of comorbidity associated with autism spectrum disorder (ASD). These comorbid conditions may add further impairments to individuals with autism and are substantially more prevalent compared to neurotypical populations. These high rates of comorbidity are not surprising taking into account the overlap of symptoms that ASD shares with other pathologies. From a research perspective, this suggests common molecular mechanisms involved in these conditions. Therefore, identifying crucial genes in the overlap between ASD and these comorbid disorders may help unravel the common biological processes involved and, ultimately, shed some light in the understanding of autism etiology. RESULTS: In this work, we used a two-fold systems biology approach specially focused on biological processes and gene networks to conduct a comparative analysis of autism with 31 frequently comorbid disorders in order to define a multi-disorder subcomponent of ASD and predict new genes of potential relevance to ASD etiology. We validated our predictions by determining the significance of our candidate genes in high throughput transcriptome expression profiling studies. Using prior knowledge of disease-related biological processes and the interaction networks of the disorders related to autism, we identified a set of 19 genes not previously linked to ASD that were significantly differentially regulated in individuals with autism. In addition, these genes were of potential etiologic relevance to autism, given their enriched roles in neurological processes crucial for optimal brain development and function, learning and memory, cognition and social behavior. CONCLUSIONS: Taken together, our approach represents a novel perspective of autism from the point of view of related comorbid disorders and proposes a model by which prior knowledge of interaction networks may enlighten and focus the genome-wide search for autism candidate genes to better define the genetic heterogeneity of ASD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3667-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-53993932017-04-24 Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes Diaz-Beltran, Leticia Esteban, Francisco J. Varma, Maya Ortuzk, Alp David, Maude Wall, Dennis P. BMC Genomics Research Article BACKGROUND: Numerous studies have highlighted the elevated degree of comorbidity associated with autism spectrum disorder (ASD). These comorbid conditions may add further impairments to individuals with autism and are substantially more prevalent compared to neurotypical populations. These high rates of comorbidity are not surprising taking into account the overlap of symptoms that ASD shares with other pathologies. From a research perspective, this suggests common molecular mechanisms involved in these conditions. Therefore, identifying crucial genes in the overlap between ASD and these comorbid disorders may help unravel the common biological processes involved and, ultimately, shed some light in the understanding of autism etiology. RESULTS: In this work, we used a two-fold systems biology approach specially focused on biological processes and gene networks to conduct a comparative analysis of autism with 31 frequently comorbid disorders in order to define a multi-disorder subcomponent of ASD and predict new genes of potential relevance to ASD etiology. We validated our predictions by determining the significance of our candidate genes in high throughput transcriptome expression profiling studies. Using prior knowledge of disease-related biological processes and the interaction networks of the disorders related to autism, we identified a set of 19 genes not previously linked to ASD that were significantly differentially regulated in individuals with autism. In addition, these genes were of potential etiologic relevance to autism, given their enriched roles in neurological processes crucial for optimal brain development and function, learning and memory, cognition and social behavior. CONCLUSIONS: Taken together, our approach represents a novel perspective of autism from the point of view of related comorbid disorders and proposes a model by which prior knowledge of interaction networks may enlighten and focus the genome-wide search for autism candidate genes to better define the genetic heterogeneity of ASD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3667-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-20 /pmc/articles/PMC5399393/ /pubmed/28427329 http://dx.doi.org/10.1186/s12864-017-3667-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Diaz-Beltran, Leticia
Esteban, Francisco J.
Varma, Maya
Ortuzk, Alp
David, Maude
Wall, Dennis P.
Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
title Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
title_full Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
title_fullStr Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
title_full_unstemmed Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
title_short Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
title_sort cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399393/
https://www.ncbi.nlm.nih.gov/pubmed/28427329
http://dx.doi.org/10.1186/s12864-017-3667-9
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