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FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study

BACKGROUND AND AIMS: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by language impairment, and challenges with social interaction, communication, and repetitive behaviors. Although genetics are a primary cause of ASD, the exact genes and molecular mechanisms involved...

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Autores principales: Haghighatfard, Arvin, Yaghoubi asl, Elham, Bahadori, Rosita Azar, Aliabadian, Rojina, Farhadi, Mahdi, Mohammadpour, Fatemeh, Tabrizi, Zeinab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620679/
https://www.ncbi.nlm.nih.gov/pubmed/36382065
http://dx.doi.org/10.1177/23969415221126391
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author Haghighatfard, Arvin
Yaghoubi asl, Elham
Bahadori, Rosita Azar
Aliabadian, Rojina
Farhadi, Mahdi
Mohammadpour, Fatemeh
Tabrizi, Zeinab
author_facet Haghighatfard, Arvin
Yaghoubi asl, Elham
Bahadori, Rosita Azar
Aliabadian, Rojina
Farhadi, Mahdi
Mohammadpour, Fatemeh
Tabrizi, Zeinab
author_sort Haghighatfard, Arvin
collection PubMed
description BACKGROUND AND AIMS: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by language impairment, and challenges with social interaction, communication, and repetitive behaviors. Although genetics are a primary cause of ASD, the exact genes and molecular mechanisms involved in its pathogenesis are not completely clear. The FOXP2 gene encodes a transcription factor that is known for its major role in language development and severe speech problems. The present study aimed to evaluate the role of FOXP2 in ASD etiology, executive functions, and brain activities. METHODS: In the present study, we recruited 450 children with ASD and 490 neurotypical control children. Three domains of executive functions (working memory, response inhibition, and vigilance) were assessed. In addition, five-minute eyes closed electroencephalography was obtained from some of the children with ASD and neurotypical children. DNA sequence and expression level of FOXP2 in blood samples of children with ASD and the control group were evaluated by using sequencing and Real-time PCR, respectively. RESULTS: The results showed no mutations but a significant down expression of FOXP2 genes in children with ASD vs. neurotypical children. Several cognitive and executive function deficiencies were detected in children with ASD. Low alpha and gamma bands in the frontal lobe and high theta bands in the occipital lobe were revealed in children with ASD. We also found several correlations between FOXP2 expression levels and clinical assessments. CONCLUSIONS: Our finding revealed the down expression of FOXP2, which could be considered as a biomarker for ASD as well as cognitive and executive dysfunction. Based on brain mapping data, FOXP2 may be related to the theta wave abnormality of children with ASD. FOXP2 may be considered a target of novel treatment to improve memory and executive functions. IMPLICATIONS: Our findings highlight the role of FOXP2 mRNA level in ASD etiology, executive functions, and brain wave frequencies.
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spelling pubmed-96206792022-11-14 FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study Haghighatfard, Arvin Yaghoubi asl, Elham Bahadori, Rosita Azar Aliabadian, Rojina Farhadi, Mahdi Mohammadpour, Fatemeh Tabrizi, Zeinab Autism Dev Lang Impair Research Article BACKGROUND AND AIMS: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by language impairment, and challenges with social interaction, communication, and repetitive behaviors. Although genetics are a primary cause of ASD, the exact genes and molecular mechanisms involved in its pathogenesis are not completely clear. The FOXP2 gene encodes a transcription factor that is known for its major role in language development and severe speech problems. The present study aimed to evaluate the role of FOXP2 in ASD etiology, executive functions, and brain activities. METHODS: In the present study, we recruited 450 children with ASD and 490 neurotypical control children. Three domains of executive functions (working memory, response inhibition, and vigilance) were assessed. In addition, five-minute eyes closed electroencephalography was obtained from some of the children with ASD and neurotypical children. DNA sequence and expression level of FOXP2 in blood samples of children with ASD and the control group were evaluated by using sequencing and Real-time PCR, respectively. RESULTS: The results showed no mutations but a significant down expression of FOXP2 genes in children with ASD vs. neurotypical children. Several cognitive and executive function deficiencies were detected in children with ASD. Low alpha and gamma bands in the frontal lobe and high theta bands in the occipital lobe were revealed in children with ASD. We also found several correlations between FOXP2 expression levels and clinical assessments. CONCLUSIONS: Our finding revealed the down expression of FOXP2, which could be considered as a biomarker for ASD as well as cognitive and executive dysfunction. Based on brain mapping data, FOXP2 may be related to the theta wave abnormality of children with ASD. FOXP2 may be considered a target of novel treatment to improve memory and executive functions. IMPLICATIONS: Our findings highlight the role of FOXP2 mRNA level in ASD etiology, executive functions, and brain wave frequencies. SAGE Publications 2022-09-22 /pmc/articles/PMC9620679/ /pubmed/36382065 http://dx.doi.org/10.1177/23969415221126391 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Article
Haghighatfard, Arvin
Yaghoubi asl, Elham
Bahadori, Rosita Azar
Aliabadian, Rojina
Farhadi, Mahdi
Mohammadpour, Fatemeh
Tabrizi, Zeinab
FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study
title FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study
title_full FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study
title_fullStr FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study
title_full_unstemmed FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study
title_short FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study
title_sort foxp2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in autism spectrum disorder; a neuroimaging genetic study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620679/
https://www.ncbi.nlm.nih.gov/pubmed/36382065
http://dx.doi.org/10.1177/23969415221126391
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