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Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder

Environmental factors contribute to risk of bipolar disorder (BD), but how environmental factors impact the development of psychopathology within the context of elevated genetic risk is unknown. We herein sought to identify epigenetic signatures operating in the context of polygenic risk for BD in y...

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Autores principales: Hesam-Shariati, Sonia, Overs, Bronwyn J., Roberts, Gloria, Toma, Claudio, Watkeys, Oliver J., Green, Melissa J., Pierce, Kerrie D., Edenberg, Howard J., Wilcox, Holly C., Stapp, Emma K., McInnis, Melvin G., Hulvershorn, Leslie A., Nurnberger, John I., Schofield, Peter R., Mitchell, Philip B., Fullerton, Janice M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349272/
https://www.ncbi.nlm.nih.gov/pubmed/35922419
http://dx.doi.org/10.1038/s41398-022-02079-6
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author Hesam-Shariati, Sonia
Overs, Bronwyn J.
Roberts, Gloria
Toma, Claudio
Watkeys, Oliver J.
Green, Melissa J.
Pierce, Kerrie D.
Edenberg, Howard J.
Wilcox, Holly C.
Stapp, Emma K.
McInnis, Melvin G.
Hulvershorn, Leslie A.
Nurnberger, John I.
Schofield, Peter R.
Mitchell, Philip B.
Fullerton, Janice M.
author_facet Hesam-Shariati, Sonia
Overs, Bronwyn J.
Roberts, Gloria
Toma, Claudio
Watkeys, Oliver J.
Green, Melissa J.
Pierce, Kerrie D.
Edenberg, Howard J.
Wilcox, Holly C.
Stapp, Emma K.
McInnis, Melvin G.
Hulvershorn, Leslie A.
Nurnberger, John I.
Schofield, Peter R.
Mitchell, Philip B.
Fullerton, Janice M.
author_sort Hesam-Shariati, Sonia
collection PubMed
description Environmental factors contribute to risk of bipolar disorder (BD), but how environmental factors impact the development of psychopathology within the context of elevated genetic risk is unknown. We herein sought to identify epigenetic signatures operating in the context of polygenic risk for BD in young people at high familial risk (HR) of BD. Peripheral blood-derived DNA was assayed using Illumina PsychArray, and Methylation-450K or -EPIC BeadChips. Polygenic risk scores (PRS) were calculated using summary statistics from recent genome-wide association studies for BD, major depressive disorder (MDD) and cross-disorder (meta-analysis of eight psychiatric disorders). Unrelated HR participants of European ancestry (n = 103) were stratified based on their BD-PRS score within the HR-population distribution, and the top two quintiles (High-BD-PRS; n = 41) compared against the bottom two quintiles (Low-BD-PRS; n = 41). The High-BD-PRS stratum also had higher mean cross-disorder-PRS and MDD-PRS (ANCOVA p = 0.035 and p = 0.024, respectively). We evaluated DNA methylation differences between High-BD-PRS and Low-BD-PRS strata using linear models. One differentially methylated probe (DMP) (cg00933603; p = 3.54 × 10(−7)) in VARS2, a mitochondrial aminoacyl-tRNA synthetase, remained significantly hypomethylated after multiple-testing correction. Overall, BD-PRS appeared to broadly impact epigenetic processes, with 1,183 genes mapped to nominal DMPs (p < 0.05); these displayed convergence with genes previously associated with BD, schizophrenia, chronotype, and risk taking. We tested poly-methylomic epigenetic profiles derived from nominal DMPs in two independent samples (n = 54 and n = 82, respectively), and conducted an exploratory evaluation of the effects of family environment, indexing cohesion and flexibility. This study highlights an important interplay between heritable risk and epigenetic factors, which warrant further exploration.
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spelling pubmed-93492722022-08-05 Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder Hesam-Shariati, Sonia Overs, Bronwyn J. Roberts, Gloria Toma, Claudio Watkeys, Oliver J. Green, Melissa J. Pierce, Kerrie D. Edenberg, Howard J. Wilcox, Holly C. Stapp, Emma K. McInnis, Melvin G. Hulvershorn, Leslie A. Nurnberger, John I. Schofield, Peter R. Mitchell, Philip B. Fullerton, Janice M. Transl Psychiatry Article Environmental factors contribute to risk of bipolar disorder (BD), but how environmental factors impact the development of psychopathology within the context of elevated genetic risk is unknown. We herein sought to identify epigenetic signatures operating in the context of polygenic risk for BD in young people at high familial risk (HR) of BD. Peripheral blood-derived DNA was assayed using Illumina PsychArray, and Methylation-450K or -EPIC BeadChips. Polygenic risk scores (PRS) were calculated using summary statistics from recent genome-wide association studies for BD, major depressive disorder (MDD) and cross-disorder (meta-analysis of eight psychiatric disorders). Unrelated HR participants of European ancestry (n = 103) were stratified based on their BD-PRS score within the HR-population distribution, and the top two quintiles (High-BD-PRS; n = 41) compared against the bottom two quintiles (Low-BD-PRS; n = 41). The High-BD-PRS stratum also had higher mean cross-disorder-PRS and MDD-PRS (ANCOVA p = 0.035 and p = 0.024, respectively). We evaluated DNA methylation differences between High-BD-PRS and Low-BD-PRS strata using linear models. One differentially methylated probe (DMP) (cg00933603; p = 3.54 × 10(−7)) in VARS2, a mitochondrial aminoacyl-tRNA synthetase, remained significantly hypomethylated after multiple-testing correction. Overall, BD-PRS appeared to broadly impact epigenetic processes, with 1,183 genes mapped to nominal DMPs (p < 0.05); these displayed convergence with genes previously associated with BD, schizophrenia, chronotype, and risk taking. We tested poly-methylomic epigenetic profiles derived from nominal DMPs in two independent samples (n = 54 and n = 82, respectively), and conducted an exploratory evaluation of the effects of family environment, indexing cohesion and flexibility. This study highlights an important interplay between heritable risk and epigenetic factors, which warrant further exploration. Nature Publishing Group UK 2022-08-03 /pmc/articles/PMC9349272/ /pubmed/35922419 http://dx.doi.org/10.1038/s41398-022-02079-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hesam-Shariati, Sonia
Overs, Bronwyn J.
Roberts, Gloria
Toma, Claudio
Watkeys, Oliver J.
Green, Melissa J.
Pierce, Kerrie D.
Edenberg, Howard J.
Wilcox, Holly C.
Stapp, Emma K.
McInnis, Melvin G.
Hulvershorn, Leslie A.
Nurnberger, John I.
Schofield, Peter R.
Mitchell, Philip B.
Fullerton, Janice M.
Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder
title Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder
title_full Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder
title_fullStr Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder
title_full_unstemmed Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder
title_short Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder
title_sort epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349272/
https://www.ncbi.nlm.nih.gov/pubmed/35922419
http://dx.doi.org/10.1038/s41398-022-02079-6
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