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First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults

CONTEXT: Prenatal dexamethasone (DEX) treatment is sometimes used in pregnancies at risk for congenital adrenal hyperplasia (CAH) to prevent virilization in female fetuses with CAH. In boys and in fetuses not having CAH, there is no benefit of early DEX treatment and the risks of this therapy must b...

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Autores principales: van’t Westeinde, Annelies, Zimmermann, Marius, Messina, Valeria, Karlsson, Leif, Padilla, Nelly, Lajic, Svetlana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510958/
https://www.ncbi.nlm.nih.gov/pubmed/32869847
http://dx.doi.org/10.1210/clinem/dgaa611
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author van’t Westeinde, Annelies
Zimmermann, Marius
Messina, Valeria
Karlsson, Leif
Padilla, Nelly
Lajic, Svetlana
author_facet van’t Westeinde, Annelies
Zimmermann, Marius
Messina, Valeria
Karlsson, Leif
Padilla, Nelly
Lajic, Svetlana
author_sort van’t Westeinde, Annelies
collection PubMed
description CONTEXT: Prenatal dexamethasone (DEX) treatment is sometimes used in pregnancies at risk for congenital adrenal hyperplasia (CAH) to prevent virilization in female fetuses with CAH. In boys and in fetuses not having CAH, there is no benefit of early DEX treatment and the risks of this therapy must be thoroughly investigated. High doses of prenatal glucocorticoid might alter the developmental trajectory of the brain into adulthood, even for CAH unaffected subjects treated with DEX for a short term during the first trimester. OBJECTIVE: The present study investigated brain activation during working memory performance in DEX-treated subjects compared with controls. DESIGN, SETTING, AND PARTICIPANTS: We tested 18 participants who were exposed to DEX during the first trimester of fetal life but did not have CAH (8 females; mean age 20.78 [standard deviation (SD), 2.67] years) and 40 control participants (24 females; mean age 20.53 [SD, 2.64]) from a single research institute. Participants underwent functional magnetic resonance imaging on a 3T scanner during a verbal and visuospatial working memory task. RESULTS: We did not observe any differences in brain activity during working memory performance. However, DEX-treated subjects responded faster during the experimental condition of the verbal WM task. CONCLUSIONS: First trimester DEX treatment did not seem to result in altered working memory–related brain activity at adult age. Our findings contribute to the risk–benefit assessment of prenatal DEX treatment in the context of CAH.
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spelling pubmed-75109582020-09-29 First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults van’t Westeinde, Annelies Zimmermann, Marius Messina, Valeria Karlsson, Leif Padilla, Nelly Lajic, Svetlana J Clin Endocrinol Metab Clinical Research Articles CONTEXT: Prenatal dexamethasone (DEX) treatment is sometimes used in pregnancies at risk for congenital adrenal hyperplasia (CAH) to prevent virilization in female fetuses with CAH. In boys and in fetuses not having CAH, there is no benefit of early DEX treatment and the risks of this therapy must be thoroughly investigated. High doses of prenatal glucocorticoid might alter the developmental trajectory of the brain into adulthood, even for CAH unaffected subjects treated with DEX for a short term during the first trimester. OBJECTIVE: The present study investigated brain activation during working memory performance in DEX-treated subjects compared with controls. DESIGN, SETTING, AND PARTICIPANTS: We tested 18 participants who were exposed to DEX during the first trimester of fetal life but did not have CAH (8 females; mean age 20.78 [standard deviation (SD), 2.67] years) and 40 control participants (24 females; mean age 20.53 [SD, 2.64]) from a single research institute. Participants underwent functional magnetic resonance imaging on a 3T scanner during a verbal and visuospatial working memory task. RESULTS: We did not observe any differences in brain activity during working memory performance. However, DEX-treated subjects responded faster during the experimental condition of the verbal WM task. CONCLUSIONS: First trimester DEX treatment did not seem to result in altered working memory–related brain activity at adult age. Our findings contribute to the risk–benefit assessment of prenatal DEX treatment in the context of CAH. Oxford University Press 2020-09-01 /pmc/articles/PMC7510958/ /pubmed/32869847 http://dx.doi.org/10.1210/clinem/dgaa611 Text en © Endocrine Society 2020. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research Articles
van’t Westeinde, Annelies
Zimmermann, Marius
Messina, Valeria
Karlsson, Leif
Padilla, Nelly
Lajic, Svetlana
First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults
title First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults
title_full First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults
title_fullStr First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults
title_full_unstemmed First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults
title_short First Trimester DEX Treatment Is Not Associated with Altered Brain Activity During Working Memory Performance in Adults
title_sort first trimester dex treatment is not associated with altered brain activity during working memory performance in adults
topic Clinical Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510958/
https://www.ncbi.nlm.nih.gov/pubmed/32869847
http://dx.doi.org/10.1210/clinem/dgaa611
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