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Associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory
Prenatal maternal distress—an umbrella concept encompassing multiple negative psychological states including stress, anxiety, and depression—is a substantial prenatal exposure. Consistent across preclinical and human studies, the hippocampus displays alterations due to prenatal distress. Nevertheles...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297970/ https://www.ncbi.nlm.nih.gov/pubmed/32305039 http://dx.doi.org/10.1038/s41386-020-0677-0 |
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author | Scheinost, Dustin Spann, Marisa N. McDonough, Laraine Peterson, Bradley S. Monk, Catherine |
author_facet | Scheinost, Dustin Spann, Marisa N. McDonough, Laraine Peterson, Bradley S. Monk, Catherine |
author_sort | Scheinost, Dustin |
collection | PubMed |
description | Prenatal maternal distress—an umbrella concept encompassing multiple negative psychological states including stress, anxiety, and depression—is a substantial prenatal exposure. Consistent across preclinical and human studies, the hippocampus displays alterations due to prenatal distress. Nevertheless, most prenatal distress studies do not focus on multiple dimensions of, have not examined hippocampal functional connectivity in association with, and do not consider observer-based functional outcomes related to distress. We investigated the effects of different dimensions of prenatal distress in pregnant adolescents, a population at high risk for distress, in association with neonatal hippocampal connectivity and infant memory. In pregnant adolescents (n = 42), we collected four measures of distress (perceived stress, depression, pregnancy-specific distress, and 24-h ambulatory salivary cortisol) during the 2nd and 3rd trimesters. Resting-state imaging data were acquired in their infants at 40–44 weeks post-menstrual age. Functional connectivity was measured from hippocampal seeds. Memory abilities were obtained at 4 months using the mobile conjugate reinforcement task. Shared across different dimensions of maternal distress, increased 3rd trimester maternal distress associated with weaker hippocampal–cingulate cortex connectivity and stronger hippocampal–temporal lobe connectivity. Perceived stress inversely correlated while hippocampal–cingulate cortex connectivity positively correlated with infant memory. Increased cortisol—collected during the 2nd, but not the 3rd, trimester—associated with weaker hippocampal–cingulate cortex connectivity and stronger hippocampal–temporal lobe connectivity. Different dimensions of prenatal maternal distress likely contribute shared and unique effects to shaping infant brain and behavior. |
format | Online Article Text |
id | pubmed-7297970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-72979702020-06-19 Associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory Scheinost, Dustin Spann, Marisa N. McDonough, Laraine Peterson, Bradley S. Monk, Catherine Neuropsychopharmacology Article Prenatal maternal distress—an umbrella concept encompassing multiple negative psychological states including stress, anxiety, and depression—is a substantial prenatal exposure. Consistent across preclinical and human studies, the hippocampus displays alterations due to prenatal distress. Nevertheless, most prenatal distress studies do not focus on multiple dimensions of, have not examined hippocampal functional connectivity in association with, and do not consider observer-based functional outcomes related to distress. We investigated the effects of different dimensions of prenatal distress in pregnant adolescents, a population at high risk for distress, in association with neonatal hippocampal connectivity and infant memory. In pregnant adolescents (n = 42), we collected four measures of distress (perceived stress, depression, pregnancy-specific distress, and 24-h ambulatory salivary cortisol) during the 2nd and 3rd trimesters. Resting-state imaging data were acquired in their infants at 40–44 weeks post-menstrual age. Functional connectivity was measured from hippocampal seeds. Memory abilities were obtained at 4 months using the mobile conjugate reinforcement task. Shared across different dimensions of maternal distress, increased 3rd trimester maternal distress associated with weaker hippocampal–cingulate cortex connectivity and stronger hippocampal–temporal lobe connectivity. Perceived stress inversely correlated while hippocampal–cingulate cortex connectivity positively correlated with infant memory. Increased cortisol—collected during the 2nd, but not the 3rd, trimester—associated with weaker hippocampal–cingulate cortex connectivity and stronger hippocampal–temporal lobe connectivity. Different dimensions of prenatal maternal distress likely contribute shared and unique effects to shaping infant brain and behavior. Springer International Publishing 2020-04-18 2020-07 /pmc/articles/PMC7297970/ /pubmed/32305039 http://dx.doi.org/10.1038/s41386-020-0677-0 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Scheinost, Dustin Spann, Marisa N. McDonough, Laraine Peterson, Bradley S. Monk, Catherine Associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory |
title | Associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory |
title_full | Associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory |
title_fullStr | Associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory |
title_full_unstemmed | Associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory |
title_short | Associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory |
title_sort | associations between different dimensions of prenatal distress, neonatal hippocampal connectivity, and infant memory |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297970/ https://www.ncbi.nlm.nih.gov/pubmed/32305039 http://dx.doi.org/10.1038/s41386-020-0677-0 |
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