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Attention-deficit/hyperactive disorder updates
BACKGROUND: Attention-deficit/hyperactive disorder (ADHD) is a neurodevelopmental disorder that commonly occurs in children with a prevalence ranging from 3.4 to 7.2%. It profoundly affects academic achievement, well-being, and social interactions. As a result, this disorder is of high cost to both...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532551/ https://www.ncbi.nlm.nih.gov/pubmed/36211978 http://dx.doi.org/10.3389/fnmol.2022.925049 |
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author | Kessi, Miriam Duan, Haolin Xiong, Juan Chen, Baiyu He, Fang Yang, Lifen Ma, Yanli Bamgbade, Olumuyiwa A. Peng, Jing Yin, Fei |
author_facet | Kessi, Miriam Duan, Haolin Xiong, Juan Chen, Baiyu He, Fang Yang, Lifen Ma, Yanli Bamgbade, Olumuyiwa A. Peng, Jing Yin, Fei |
author_sort | Kessi, Miriam |
collection | PubMed |
description | BACKGROUND: Attention-deficit/hyperactive disorder (ADHD) is a neurodevelopmental disorder that commonly occurs in children with a prevalence ranging from 3.4 to 7.2%. It profoundly affects academic achievement, well-being, and social interactions. As a result, this disorder is of high cost to both individuals and society. Despite the availability of knowledge regarding the mechanisms of ADHD, the pathogenesis is not clear, hence, the existence of many challenges especially in making correct early diagnosis and provision of accurate management. OBJECTIVES: We aimed to review the pathogenic pathways of ADHD in children. The major focus was to provide an update on the reported etiologies in humans, animal models, modulators, therapies, mechanisms, epigenetic changes, and the interaction between genetic and environmental factors. METHODS: References for this review were identified through a systematic search in PubMed by using special keywords for all years until January 2022. RESULTS: Several genes have been reported to associate with ADHD: DRD1, DRD2, DRD4, DAT1, TPH2, HTR1A, HTR1B, SLC6A4, HTR2A, DBH, NET1, ADRA2A, ADRA2C, CHRNA4, CHRNA7, GAD1, GRM1, GRM5, GRM7, GRM8, TARBP1, ADGRL3, FGF1, MAOA, BDNF, SNAP25, STX1A, ATXN7, and SORCS2. Some of these genes have evidence both from human beings and animal models, while others have evidence in either humans or animal models only. Notably, most of these animal models are knockout and do not generate the genetic alteration of the patients. Besides, some of the gene polymorphisms reported differ according to the ethnic groups. The majority of the available animal models are related to the dopaminergic pathway. Epigenetic changes including SUMOylation, methylation, and acetylation have been reported in genes related to the dopaminergic pathway. CONCLUSION: The dopaminergic pathway remains to be crucial in the pathogenesis of ADHD. It can be affected by environmental factors and other pathways. Nevertheless, it is still unclear how environmental factors relate to all neurotransmitter pathways; thus, more studies are needed. Although several genes have been related to ADHD, there are few animal model studies on the majority of the genes, and they do not generate the genetic alteration of the patients. More animal models and epigenetic studies are required. |
format | Online Article Text |
id | pubmed-9532551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95325512022-10-06 Attention-deficit/hyperactive disorder updates Kessi, Miriam Duan, Haolin Xiong, Juan Chen, Baiyu He, Fang Yang, Lifen Ma, Yanli Bamgbade, Olumuyiwa A. Peng, Jing Yin, Fei Front Mol Neurosci Neuroscience BACKGROUND: Attention-deficit/hyperactive disorder (ADHD) is a neurodevelopmental disorder that commonly occurs in children with a prevalence ranging from 3.4 to 7.2%. It profoundly affects academic achievement, well-being, and social interactions. As a result, this disorder is of high cost to both individuals and society. Despite the availability of knowledge regarding the mechanisms of ADHD, the pathogenesis is not clear, hence, the existence of many challenges especially in making correct early diagnosis and provision of accurate management. OBJECTIVES: We aimed to review the pathogenic pathways of ADHD in children. The major focus was to provide an update on the reported etiologies in humans, animal models, modulators, therapies, mechanisms, epigenetic changes, and the interaction between genetic and environmental factors. METHODS: References for this review were identified through a systematic search in PubMed by using special keywords for all years until January 2022. RESULTS: Several genes have been reported to associate with ADHD: DRD1, DRD2, DRD4, DAT1, TPH2, HTR1A, HTR1B, SLC6A4, HTR2A, DBH, NET1, ADRA2A, ADRA2C, CHRNA4, CHRNA7, GAD1, GRM1, GRM5, GRM7, GRM8, TARBP1, ADGRL3, FGF1, MAOA, BDNF, SNAP25, STX1A, ATXN7, and SORCS2. Some of these genes have evidence both from human beings and animal models, while others have evidence in either humans or animal models only. Notably, most of these animal models are knockout and do not generate the genetic alteration of the patients. Besides, some of the gene polymorphisms reported differ according to the ethnic groups. The majority of the available animal models are related to the dopaminergic pathway. Epigenetic changes including SUMOylation, methylation, and acetylation have been reported in genes related to the dopaminergic pathway. CONCLUSION: The dopaminergic pathway remains to be crucial in the pathogenesis of ADHD. It can be affected by environmental factors and other pathways. Nevertheless, it is still unclear how environmental factors relate to all neurotransmitter pathways; thus, more studies are needed. Although several genes have been related to ADHD, there are few animal model studies on the majority of the genes, and they do not generate the genetic alteration of the patients. More animal models and epigenetic studies are required. Frontiers Media S.A. 2022-09-21 /pmc/articles/PMC9532551/ /pubmed/36211978 http://dx.doi.org/10.3389/fnmol.2022.925049 Text en Copyright © 2022 Kessi, Duan, Xiong, Chen, He, Yang, Ma, Bamgbade, Peng and Yin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Kessi, Miriam Duan, Haolin Xiong, Juan Chen, Baiyu He, Fang Yang, Lifen Ma, Yanli Bamgbade, Olumuyiwa A. Peng, Jing Yin, Fei Attention-deficit/hyperactive disorder updates |
title | Attention-deficit/hyperactive disorder updates |
title_full | Attention-deficit/hyperactive disorder updates |
title_fullStr | Attention-deficit/hyperactive disorder updates |
title_full_unstemmed | Attention-deficit/hyperactive disorder updates |
title_short | Attention-deficit/hyperactive disorder updates |
title_sort | attention-deficit/hyperactive disorder updates |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532551/ https://www.ncbi.nlm.nih.gov/pubmed/36211978 http://dx.doi.org/10.3389/fnmol.2022.925049 |
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