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Altered immune phenotype and DNA methylation in panic disorder

BACKGROUND: Multiple studies have related psychiatric disorders and immune alterations. Panic disorder (PD) has been linked with changes in leukocytes distributions in several small studies using different methods for immune characterization. Additionally, alterations in the methylation of repetitiv...

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Autores principales: Petersen, Curtis L., Chen, Ji-Qing, Salas, Lucas A., Christensen, Brock C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672933/
https://www.ncbi.nlm.nih.gov/pubmed/33208194
http://dx.doi.org/10.1186/s13148-020-00972-9
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author Petersen, Curtis L.
Chen, Ji-Qing
Salas, Lucas A.
Christensen, Brock C.
author_facet Petersen, Curtis L.
Chen, Ji-Qing
Salas, Lucas A.
Christensen, Brock C.
author_sort Petersen, Curtis L.
collection PubMed
description BACKGROUND: Multiple studies have related psychiatric disorders and immune alterations. Panic disorder (PD) has been linked with changes in leukocytes distributions in several small studies using different methods for immune characterization. Additionally, alterations in the methylation of repetitive DNA elements, such as LINE-1, have been associated with mental disorders. Here, we use peripheral blood DNA methylation data from two studies and an updated DNA methylation deconvolution library to investigate the relation of leukocyte proportions and methylation status of repetitive elements in 133 patients with panic disorder compared with 118 controls. METHODS AND RESULTS: We used DNA methylation data to deconvolute leukocyte cell-type proportions and to infer LINE-1 element methylation comparing PD cases and controls. We also identified differentially methylated CpGs associated with PD using an epigenome-wide association study approach (EWAS), with models adjusting for sex, age, and cell-type proportions. Individuals with PD had a lower proportion of CD8T cells (OR: 0.86, 95% CI: 0.78–0.96, P-adj = 0.030) when adjusting for age, sex, and study compared with controls. Also, PD cases had significantly lower LINE-1 repetitive element methylation than controls (P < 0.001). The EWAS identified 61 differentially methylated CpGs (58 hypo- and 3 hypermethylated) in PD (Bonferroni adjusted P < 1.33 × 10(–7)). CONCLUSIONS: These results suggest that those with panic disorder have changes to their immune system and dysregulation of repeat elements relative to controls.
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spelling pubmed-76729332020-11-19 Altered immune phenotype and DNA methylation in panic disorder Petersen, Curtis L. Chen, Ji-Qing Salas, Lucas A. Christensen, Brock C. Clin Epigenetics Research BACKGROUND: Multiple studies have related psychiatric disorders and immune alterations. Panic disorder (PD) has been linked with changes in leukocytes distributions in several small studies using different methods for immune characterization. Additionally, alterations in the methylation of repetitive DNA elements, such as LINE-1, have been associated with mental disorders. Here, we use peripheral blood DNA methylation data from two studies and an updated DNA methylation deconvolution library to investigate the relation of leukocyte proportions and methylation status of repetitive elements in 133 patients with panic disorder compared with 118 controls. METHODS AND RESULTS: We used DNA methylation data to deconvolute leukocyte cell-type proportions and to infer LINE-1 element methylation comparing PD cases and controls. We also identified differentially methylated CpGs associated with PD using an epigenome-wide association study approach (EWAS), with models adjusting for sex, age, and cell-type proportions. Individuals with PD had a lower proportion of CD8T cells (OR: 0.86, 95% CI: 0.78–0.96, P-adj = 0.030) when adjusting for age, sex, and study compared with controls. Also, PD cases had significantly lower LINE-1 repetitive element methylation than controls (P < 0.001). The EWAS identified 61 differentially methylated CpGs (58 hypo- and 3 hypermethylated) in PD (Bonferroni adjusted P < 1.33 × 10(–7)). CONCLUSIONS: These results suggest that those with panic disorder have changes to their immune system and dysregulation of repeat elements relative to controls. BioMed Central 2020-11-18 /pmc/articles/PMC7672933/ /pubmed/33208194 http://dx.doi.org/10.1186/s13148-020-00972-9 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Petersen, Curtis L.
Chen, Ji-Qing
Salas, Lucas A.
Christensen, Brock C.
Altered immune phenotype and DNA methylation in panic disorder
title Altered immune phenotype and DNA methylation in panic disorder
title_full Altered immune phenotype and DNA methylation in panic disorder
title_fullStr Altered immune phenotype and DNA methylation in panic disorder
title_full_unstemmed Altered immune phenotype and DNA methylation in panic disorder
title_short Altered immune phenotype and DNA methylation in panic disorder
title_sort altered immune phenotype and dna methylation in panic disorder
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672933/
https://www.ncbi.nlm.nih.gov/pubmed/33208194
http://dx.doi.org/10.1186/s13148-020-00972-9
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