Common genetic aspects between Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder
integrative review
DOI:
https://doi.org/10.56102/afmo.2023.245Keywords:
Autism Spectrum Disorder, Attention Deficit Hyperactivity Disorder, Mutations, GenesAbstract
Objective: The selected studies were analyzed descriptively regarding the common genetic etiology of autism spectrum disorder and attention deficit hyperactivity disorder, allowing for observing, describing, and classifying the data. Methods: We performed a review of the literature on Pubmed and Virtual Health Library (VHL) databases. The search descriptors (Autistic Disorder) OR (Autism Spectrum Disorder) AND (Deficit Disorder) of Attention with Hyperactivity) AND (Genetic Association Studies) OR (Genetics) OR (Heredity) were used in VHL; and ((“Autism Spectrum Disorder” AND “Attention Deficit Disorder with Hyperactivity”) AND (“Genetic Association Studies” OR “Genetics OR Heredity”)) were used in PubMed. Results: A total of 75 studies were identified, 54 in the VHL and 21 in the PubMed. Of these, 18 remained after screening for title and abstract. After full text reading, nine studies were included in this review. Discussion: De novo genic mutations contribute to autism spectrum disorder, and some studies support they might also be determinant for attention deficit hyperactivity disorder. The RFX3, RFX4, and RFX7 genes found in cells of the cerebral cortex of fetuses and adults contribute to linking important regions related to cognition and social behavior. Conclusion: The included studies indicate a correlation between genetic etiologies of autism spectrum disorder and attention deficit hyperactivity disorder.
References
Carlsson T, Molander F, Taylor MJ, Jonsson U, Bölte S. Early environmental risk factors for neurodevelopmental disorders - A systematic review of twin and sibling studies. Dev Psychopathol. 2021 out 28;33(4):1448–95.https://pubmed.ncbi.nlm.nih.gov/32703331/
Harris HK, Nakayama T, Lai J, Zhao B, Argyrou N, Gubbels CS, et al. Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior. Genetics in Medicine. 2021 jun 1;23(6):1028–40. https://pubmed.ncbi.nlm.nih.gov/33658631/
Björkenstam E, Pierce M, Björkenstam C, Dalman C, Kosidou K. Attention Deficit/Hyperactivity Disorder and risk for non-affective psychotic disorder: The role of ADHD medication and comorbidity, and sibling comparison. Schizophr Res. 2020 abr 1;218:124–30. https://pubmed.ncbi.nlm.nih.gov/32001080/
Okyar E, Görker I. Examining the autistic traits in children and adolescents diagnosed with attention-deficit hyperactivity disorder and their parents. BMC Psychiatry. 2020 jun 5;20(1). https://pubmed.ncbi.nlm.nih.gov/32503560/
Slob EMA, Brew BK, Vijverberg SJH, Dijs T, van Beijsterveldt CEM, Koppelman GH, et al. Early-life antibiotic use and risk of attention-deficit hyperactivity disorder and autism spectrum disorder: results of a discordant twin study. Int J Epidemiol. 2021 maio 17;50(2):475–84. https://pubmed.ncbi.nlm.nih.gov/33179025/
Patak J, Faraone S v., Zhang-James Y. Sodium hydrogen exchanger 9 NHE9 (SLC9A9) and its emerging roles in neuropsychiatric comorbidity. Vol. 183, American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. Blackwell Publishing Inc.; 2020. p. 289–305. https://pubmed.ncbi.nlm.nih.gov/32400953/
Sugiaman-Trapman D, Vitezic M, Jouhilahti EM, Mathelier A, Lauter G, Misra S, et al. Characterization of the human RFX transcription factor family by regulatory and target gene analysis. BMC Genomics. 2018 mar 6;19(1).https://pubmed.ncbi.nlm.nih.gov/29510665/
Moreau CA, Urchs SGW, Kuldeep K, Orban P, Schramm C, Dumas G, et al. Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia. Nat Commun. 2020 dez 1;11(1). https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573583/
Hall LS, Pain O, O’Brien HE, Anney R, Walters JTR, Owen MJ, et al. Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders. Mol Psychiatry. 2021 jun 1;26(6):2082–8. https://pubmed.ncbi.nlm.nih.gov/32366953/
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2023 Matheus Mastrianni Lima Medeiros, Jade Souza Martins, João Marcos da Silva Dantas, Helder Elísio Evangelista Vieira, Albert Eduardo Silva Martins

This work is licensed under a Creative Commons Attribution 4.0 International License.
Esta licença permite que outros distribuam, remixem, adaptem e desenvolvam seu trabalho, mesmo comercialmente, desde que creditem a revista pela criação original.