DNA methylation in adolescents with anxiety disorder : a longitudinal study

Detalhes bibliográficos
Autor(a) principal: Bortoluzzi, Andressa
Data de Publicação: 2018
Outros Autores: Salum Junior, Giovanni Abrahão, Rosa, Eduarda Dias da, Chagas, Vinicius de Saraiva, Castro, Mauro Antônio Alves, Manfro, Gisele Gus
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/206702
Resumo: 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 classifed 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 frst evaluation only, n=8). DNA methylation was evaluated with the Infnium 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 specifc genes relevant to AD.
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spelling Bortoluzzi, AndressaSalum Junior, Giovanni AbrahãoRosa, Eduarda Dias daChagas, Vinicius de SaraivaCastro, Mauro Antônio AlvesManfro, Gisele Gus2020-03-12T04:14:00Z20182045-2322http://hdl.handle.net/10183/206702001112652Anxiety 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 classifed 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 frst evaluation only, n=8). DNA methylation was evaluated with the Infnium 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 specifc genes relevant to AD.application/pdfengScientific reports. London. Vol.8 (2018), 13800, 12 p.Estudos longitudinaisMetilação de DNATranstornos de ansiedadeAdolescenteDNA methylation in adolescents with anxiety disorder : a longitudinal studyEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001112652.pdf.txt001112652.pdf.txtExtracted Texttext/plain55479http://www.lume.ufrgs.br/bitstream/10183/206702/2/001112652.pdf.txt81e8df6aa54da44c808d64a8a74e32c8MD52ORIGINAL001112652.pdfTexto completo (inglês)application/pdf1509767http://www.lume.ufrgs.br/bitstream/10183/206702/1/001112652.pdf8e05ee55a7f519b765bee04a24286832MD5110183/2067022020-03-13 04:16:39.016488oai:www.lume.ufrgs.br:10183/206702Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2020-03-13T07:16:39Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv DNA methylation in adolescents with anxiety disorder : a longitudinal study
title DNA methylation in adolescents with anxiety disorder : a longitudinal study
spellingShingle DNA methylation in adolescents with anxiety disorder : a longitudinal study
Bortoluzzi, Andressa
Estudos longitudinais
Metilação de DNA
Transtornos de ansiedade
Adolescente
title_short 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_sort DNA methylation in adolescents with anxiety disorder : a longitudinal study
author Bortoluzzi, Andressa
author_facet Bortoluzzi, Andressa
Salum Junior, Giovanni Abrahão
Rosa, Eduarda Dias da
Chagas, Vinicius de Saraiva
Castro, Mauro Antônio Alves
Manfro, Gisele Gus
author_role author
author2 Salum Junior, Giovanni Abrahão
Rosa, Eduarda Dias da
Chagas, Vinicius de Saraiva
Castro, Mauro Antônio Alves
Manfro, Gisele Gus
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Bortoluzzi, Andressa
Salum Junior, Giovanni Abrahão
Rosa, Eduarda Dias da
Chagas, Vinicius de Saraiva
Castro, Mauro Antônio Alves
Manfro, Gisele Gus
dc.subject.por.fl_str_mv Estudos longitudinais
Metilação de DNA
Transtornos de ansiedade
Adolescente
topic Estudos longitudinais
Metilação de DNA
Transtornos de ansiedade
Adolescente
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 classifed 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 frst evaluation only, n=8). DNA methylation was evaluated with the Infnium 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 specifc genes relevant to AD.
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dc.relation.ispartof.pt_BR.fl_str_mv Scientific reports. London. Vol.8 (2018), 13800, 12 p.
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