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DNA methylation in adolescents with anxiety disorder: a longitudinal study

Anxiety disorders (AD) typically manifest in children and adolescents and might persist into adulthood. However, there are still few data concerning epigenetic mechanisms associated with onset, persistence or remission of AD over time. We investigated a cohort of adolescents and young adults at base...

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Autores principales: Bortoluzzi, Andressa, Salum, Giovanni Abrahão, da Rosa, Eduarda Dias, Chagas, Vinicius de Saraiva, Castro, Mauro Antônio Alves, Manfro, Gisele Gus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138655/
https://www.ncbi.nlm.nih.gov/pubmed/30218003
http://dx.doi.org/10.1038/s41598-018-32090-1
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author Bortoluzzi, Andressa
Salum, Giovanni Abrahão
da Rosa, Eduarda Dias
Chagas, Vinicius de Saraiva
Castro, Mauro Antônio Alves
Manfro, Gisele Gus
author_facet Bortoluzzi, Andressa
Salum, Giovanni Abrahão
da Rosa, Eduarda Dias
Chagas, Vinicius de Saraiva
Castro, Mauro Antônio Alves
Manfro, Gisele Gus
author_sort Bortoluzzi, Andressa
collection PubMed
description Anxiety disorders (AD) typically manifest in children and adolescents and might persist into adulthood. However, there are still few data concerning epigenetic mechanisms associated with onset, persistence or remission of AD over time. We investigated a cohort of adolescents and young adults at baseline (age; 13.19 ± 2.38) and after 5 years and classified them according to the AD diagnosis and their longitudinal trajectories into 4 groups: (1) Typically Developing Comparisons (TDC; control group, n = 14); (2) Incident (AD in the second evaluation only, n = 11); (3) Persistent (AD in both evaluations, n = 14) and (4) Remittent (AD in the first evaluation only, n = 8). DNA methylation was evaluated with the Infinium HumanMethylation450 BeadChip from saliva samples collected at both evaluations. Gene set enrichment analysis was applied to consider biological pathways. We found decreased DNA methylation in TDC group while the chronic cases of AD presented hypermethylation in central nervous system development pathways. Moreover, we showed that this persistent group also presented hypermethylation while the other three groups were associated with hypomethylation in nervous system development pathway. Incidence and remission groups were associated with increased and decreased methylation in neuron development pathways, respectively. Larger studies are likely to detect specific genes relevant to AD.
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spelling pubmed-61386552018-09-15 DNA methylation in adolescents with anxiety disorder: a longitudinal study Bortoluzzi, Andressa Salum, Giovanni Abrahão da Rosa, Eduarda Dias Chagas, Vinicius de Saraiva Castro, Mauro Antônio Alves Manfro, Gisele Gus Sci Rep Article Anxiety disorders (AD) typically manifest in children and adolescents and might persist into adulthood. However, there are still few data concerning epigenetic mechanisms associated with onset, persistence or remission of AD over time. We investigated a cohort of adolescents and young adults at baseline (age; 13.19 ± 2.38) and after 5 years and classified them according to the AD diagnosis and their longitudinal trajectories into 4 groups: (1) Typically Developing Comparisons (TDC; control group, n = 14); (2) Incident (AD in the second evaluation only, n = 11); (3) Persistent (AD in both evaluations, n = 14) and (4) Remittent (AD in the first evaluation only, n = 8). DNA methylation was evaluated with the Infinium HumanMethylation450 BeadChip from saliva samples collected at both evaluations. Gene set enrichment analysis was applied to consider biological pathways. We found decreased DNA methylation in TDC group while the chronic cases of AD presented hypermethylation in central nervous system development pathways. Moreover, we showed that this persistent group also presented hypermethylation while the other three groups were associated with hypomethylation in nervous system development pathway. Incidence and remission groups were associated with increased and decreased methylation in neuron development pathways, respectively. Larger studies are likely to detect specific genes relevant to AD. Nature Publishing Group UK 2018-09-14 /pmc/articles/PMC6138655/ /pubmed/30218003 http://dx.doi.org/10.1038/s41598-018-32090-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bortoluzzi, Andressa
Salum, Giovanni Abrahão
da Rosa, Eduarda Dias
Chagas, Vinicius de Saraiva
Castro, Mauro Antônio Alves
Manfro, Gisele Gus
DNA methylation in adolescents with anxiety disorder: a longitudinal study
title DNA methylation in adolescents with anxiety disorder: a longitudinal study
title_full DNA methylation in adolescents with anxiety disorder: a longitudinal study
title_fullStr DNA methylation in adolescents with anxiety disorder: a longitudinal study
title_full_unstemmed DNA methylation in adolescents with anxiety disorder: a longitudinal study
title_short DNA methylation in adolescents with anxiety disorder: a longitudinal study
title_sort dna methylation in adolescents with anxiety disorder: a longitudinal study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138655/
https://www.ncbi.nlm.nih.gov/pubmed/30218003
http://dx.doi.org/10.1038/s41598-018-32090-1
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