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DNA methylation in cord blood in association with prenatal depressive symptoms
BACKGROUND: Prenatal symptoms of depression (PND) and anxiety affect up to every third pregnancy. Children of mothers with mental health problems are at higher risk of developmental problems, possibly through epigenetic mechanisms together with other factors such as genetic and environmental. We inv...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042709/ https://www.ncbi.nlm.nih.gov/pubmed/33845866 http://dx.doi.org/10.1186/s13148-021-01054-0 |
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author | Kallak, Theodora Kunovac Bränn, Emma Fransson, Emma Johansson, Åsa Lager, Susanne Comasco, Erika Lyle, Robert Skalkidou, Alkistis |
author_facet | Kallak, Theodora Kunovac Bränn, Emma Fransson, Emma Johansson, Åsa Lager, Susanne Comasco, Erika Lyle, Robert Skalkidou, Alkistis |
author_sort | Kallak, Theodora Kunovac |
collection | PubMed |
description | BACKGROUND: Prenatal symptoms of depression (PND) and anxiety affect up to every third pregnancy. Children of mothers with mental health problems are at higher risk of developmental problems, possibly through epigenetic mechanisms together with other factors such as genetic and environmental. We investigated DNA methylation in cord blood in relation to PND, taking into consideration a history of depression, co-morbidity with anxiety and selective serotonin reuptake inhibitors (SSRI) use, and stratified by sex of the child. Mothers (N = 373) prospectively filled out web-based questionnaires regarding mood symptoms and SSRI use throughout pregnancy. Cord blood was collected at birth and DNA methylation was measured using Illumina MethylationEPIC array at 850 000 CpG sites throughout the genome. Differentially methylated regions were identified using Kruskal–Wallis test, and Benjamini-Hochberg adjusted p-values < 0.05 were considered significant. RESULTS: No differential DNA methylation was associated with PND alone; however, differential DNA methylation was observed in children exposed to comorbid PND with anxiety symptoms compared with healthy controls in ABCF1 (log twofold change − 0.2), but not after stratification by sex of the child. DNA methylation in children exposed to PND without SSRI treatment and healthy controls both differed in comparison with SSRI exposed children at several sites and regions, among which hypomethylation was observed in CpGs in the promoter region of CRBN (log2 fold change − 0.57), involved in brain development, and hypermethylation in MDFIC (log2 fold change 0.45), associated with the glucocorticoid stress response. CONCLUSION: Although it is not possible to assess if these methylation differences are due to SSRI treatment itself or to more severe depression, our findings add on to existing knowledge that there might be different biological consequences for the child depending on whether maternal PND was treated with SSRIs or not. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01054-0. |
format | Online Article Text |
id | pubmed-8042709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80427092021-04-14 DNA methylation in cord blood in association with prenatal depressive symptoms Kallak, Theodora Kunovac Bränn, Emma Fransson, Emma Johansson, Åsa Lager, Susanne Comasco, Erika Lyle, Robert Skalkidou, Alkistis Clin Epigenetics Research BACKGROUND: Prenatal symptoms of depression (PND) and anxiety affect up to every third pregnancy. Children of mothers with mental health problems are at higher risk of developmental problems, possibly through epigenetic mechanisms together with other factors such as genetic and environmental. We investigated DNA methylation in cord blood in relation to PND, taking into consideration a history of depression, co-morbidity with anxiety and selective serotonin reuptake inhibitors (SSRI) use, and stratified by sex of the child. Mothers (N = 373) prospectively filled out web-based questionnaires regarding mood symptoms and SSRI use throughout pregnancy. Cord blood was collected at birth and DNA methylation was measured using Illumina MethylationEPIC array at 850 000 CpG sites throughout the genome. Differentially methylated regions were identified using Kruskal–Wallis test, and Benjamini-Hochberg adjusted p-values < 0.05 were considered significant. RESULTS: No differential DNA methylation was associated with PND alone; however, differential DNA methylation was observed in children exposed to comorbid PND with anxiety symptoms compared with healthy controls in ABCF1 (log twofold change − 0.2), but not after stratification by sex of the child. DNA methylation in children exposed to PND without SSRI treatment and healthy controls both differed in comparison with SSRI exposed children at several sites and regions, among which hypomethylation was observed in CpGs in the promoter region of CRBN (log2 fold change − 0.57), involved in brain development, and hypermethylation in MDFIC (log2 fold change 0.45), associated with the glucocorticoid stress response. CONCLUSION: Although it is not possible to assess if these methylation differences are due to SSRI treatment itself or to more severe depression, our findings add on to existing knowledge that there might be different biological consequences for the child depending on whether maternal PND was treated with SSRIs or not. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01054-0. BioMed Central 2021-04-12 /pmc/articles/PMC8042709/ /pubmed/33845866 http://dx.doi.org/10.1186/s13148-021-01054-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Kallak, Theodora Kunovac Bränn, Emma Fransson, Emma Johansson, Åsa Lager, Susanne Comasco, Erika Lyle, Robert Skalkidou, Alkistis DNA methylation in cord blood in association with prenatal depressive symptoms |
title | DNA methylation in cord blood in association with prenatal depressive symptoms |
title_full | DNA methylation in cord blood in association with prenatal depressive symptoms |
title_fullStr | DNA methylation in cord blood in association with prenatal depressive symptoms |
title_full_unstemmed | DNA methylation in cord blood in association with prenatal depressive symptoms |
title_short | DNA methylation in cord blood in association with prenatal depressive symptoms |
title_sort | dna methylation in cord blood in association with prenatal depressive symptoms |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042709/ https://www.ncbi.nlm.nih.gov/pubmed/33845866 http://dx.doi.org/10.1186/s13148-021-01054-0 |
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