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Identifying a biological signature of prenatal maternal stress
Psychological stress affects maternal gastrointestinal (GI) permeability, leading to low-grade inflammation, which can negatively affect fetal development. We investigated a panel of circulating markers as a biological signature of this stress exposure in pregnant women with and without the stress-r...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934857/ https://www.ncbi.nlm.nih.gov/pubmed/33301421 http://dx.doi.org/10.1172/jci.insight.143007 |
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author | Keane, James M. Khashan, Ali S. McCarthy, Fergus P. Kenny, Louise C. Collins, James M. O’Donovan, Sarah Brown, Jillian Cryan, John F. Dinan, Timothy G. Clarke, Gerard O’Mahony, Siobhain M. |
author_facet | Keane, James M. Khashan, Ali S. McCarthy, Fergus P. Kenny, Louise C. Collins, James M. O’Donovan, Sarah Brown, Jillian Cryan, John F. Dinan, Timothy G. Clarke, Gerard O’Mahony, Siobhain M. |
author_sort | Keane, James M. |
collection | PubMed |
description | Psychological stress affects maternal gastrointestinal (GI) permeability, leading to low-grade inflammation, which can negatively affect fetal development. We investigated a panel of circulating markers as a biological signature of this stress exposure in pregnant women with and without the stress-related GI disorder irritable bowel syndrome (IBS). Markers of GI permeability and inflammation were measured in plasma from healthy and IBS cohorts of women at 15 and 20 weeks’ gestation. Biomarkers were evaluated with respect to their degree of association to levels of stress, anxiety, and depression as indicated by responses from the Perceived Stress Scale, State-Trait Anxiety Inventory, and Edinburgh Postnatal Depression Scale. High levels of stress were associated with elevations of soluble CD14, lipopolysaccharide binding protein (LBP), and tumor necrosis factor–α, while anxiety was associated with elevated concentrations of C-reactive protein (CRP) in otherwise healthy pregnancies. Prenatal depression was associated with higher levels of soluble CD14, LBP, and CRP in the healthy cohort. High levels of prenatal anxiety and depression were also associated with lower concentrations of tryptophan and kynurenine, respectively, in the IBS cohort. These markers may represent a core maternal biological signature of active prenatal stress, which can be used to inform intervention strategies via stress reduction techniques or other lifestyle approaches. Such interventions may need to be tailored to reflect underlying GI conditions, such as IBS. |
format | Online Article Text |
id | pubmed-7934857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-79348572021-03-09 Identifying a biological signature of prenatal maternal stress Keane, James M. Khashan, Ali S. McCarthy, Fergus P. Kenny, Louise C. Collins, James M. O’Donovan, Sarah Brown, Jillian Cryan, John F. Dinan, Timothy G. Clarke, Gerard O’Mahony, Siobhain M. JCI Insight Research Article Psychological stress affects maternal gastrointestinal (GI) permeability, leading to low-grade inflammation, which can negatively affect fetal development. We investigated a panel of circulating markers as a biological signature of this stress exposure in pregnant women with and without the stress-related GI disorder irritable bowel syndrome (IBS). Markers of GI permeability and inflammation were measured in plasma from healthy and IBS cohorts of women at 15 and 20 weeks’ gestation. Biomarkers were evaluated with respect to their degree of association to levels of stress, anxiety, and depression as indicated by responses from the Perceived Stress Scale, State-Trait Anxiety Inventory, and Edinburgh Postnatal Depression Scale. High levels of stress were associated with elevations of soluble CD14, lipopolysaccharide binding protein (LBP), and tumor necrosis factor–α, while anxiety was associated with elevated concentrations of C-reactive protein (CRP) in otherwise healthy pregnancies. Prenatal depression was associated with higher levels of soluble CD14, LBP, and CRP in the healthy cohort. High levels of prenatal anxiety and depression were also associated with lower concentrations of tryptophan and kynurenine, respectively, in the IBS cohort. These markers may represent a core maternal biological signature of active prenatal stress, which can be used to inform intervention strategies via stress reduction techniques or other lifestyle approaches. Such interventions may need to be tailored to reflect underlying GI conditions, such as IBS. American Society for Clinical Investigation 2021-01-25 /pmc/articles/PMC7934857/ /pubmed/33301421 http://dx.doi.org/10.1172/jci.insight.143007 Text en © 2021 Keane et al. http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Keane, James M. Khashan, Ali S. McCarthy, Fergus P. Kenny, Louise C. Collins, James M. O’Donovan, Sarah Brown, Jillian Cryan, John F. Dinan, Timothy G. Clarke, Gerard O’Mahony, Siobhain M. Identifying a biological signature of prenatal maternal stress |
title | Identifying a biological signature of prenatal maternal stress |
title_full | Identifying a biological signature of prenatal maternal stress |
title_fullStr | Identifying a biological signature of prenatal maternal stress |
title_full_unstemmed | Identifying a biological signature of prenatal maternal stress |
title_short | Identifying a biological signature of prenatal maternal stress |
title_sort | identifying a biological signature of prenatal maternal stress |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934857/ https://www.ncbi.nlm.nih.gov/pubmed/33301421 http://dx.doi.org/10.1172/jci.insight.143007 |
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