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Resting-state functional connectivity in women with PMDD

BACKGROUND: Premenstrual dysphoric disorder (PMDD) is an understudied, debilitating disorder of women. Given evidence for prefrontal cortical and limbic dysfunction in PMDD, we compared intrinsic connectivity of the executive control network (ECN), default mode network (DMN), and amygdala in women w...

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Autores principales: Petersen, Nicole, Ghahremani, Dara G., Rapkin, Andrea J., Berman, Steven M., Wijker, Noor, Liang, Letty, London, Edythe D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906514/
https://www.ncbi.nlm.nih.gov/pubmed/31827073
http://dx.doi.org/10.1038/s41398-019-0670-8
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author Petersen, Nicole
Ghahremani, Dara G.
Rapkin, Andrea J.
Berman, Steven M.
Wijker, Noor
Liang, Letty
London, Edythe D.
author_facet Petersen, Nicole
Ghahremani, Dara G.
Rapkin, Andrea J.
Berman, Steven M.
Wijker, Noor
Liang, Letty
London, Edythe D.
author_sort Petersen, Nicole
collection PubMed
description BACKGROUND: Premenstrual dysphoric disorder (PMDD) is an understudied, debilitating disorder of women. Given evidence for prefrontal cortical and limbic dysfunction in PMDD, we compared intrinsic connectivity of the executive control network (ECN), default mode network (DMN), and amygdala in women with PMDD vs. controls. METHODS: Thirty-six women (18 PMDD, 18 control) participated in fMRI during the follicular and luteal phases of the menstrual cycle. At each time, resting-state functional connectivity was evaluated both before and after participants performed an emotion regulation task. The ECN was identified using independent components analysis, and connectivity of left and right amygdala seeds was also evaluated. RESULTS: Nonparametric permutation testing identified a cluster in the left middle temporal gyrus (MTG) with significantly stronger connectivity to the left ECN in women with PMDD vs. controls in all four fMRI sessions. Women with PMDD exhibited no difference in functional connectivity between menstrual cycle phases. Amygdala connectivity did not differ between the groups but differed significantly with menstrual phase, with left amygdala connectivity to cingulate cortex being significantly stronger during the follicular vs. luteal phase. Right amygdala connectivity to the middle frontal gyrus was also stronger during the follicular vs. luteal phase, with no group differences. These findings suggest that women with PMDD have different intrinsic network dynamics in the left executive control network compared to healthy controls.
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spelling pubmed-69065142019-12-13 Resting-state functional connectivity in women with PMDD Petersen, Nicole Ghahremani, Dara G. Rapkin, Andrea J. Berman, Steven M. Wijker, Noor Liang, Letty London, Edythe D. Transl Psychiatry Article BACKGROUND: Premenstrual dysphoric disorder (PMDD) is an understudied, debilitating disorder of women. Given evidence for prefrontal cortical and limbic dysfunction in PMDD, we compared intrinsic connectivity of the executive control network (ECN), default mode network (DMN), and amygdala in women with PMDD vs. controls. METHODS: Thirty-six women (18 PMDD, 18 control) participated in fMRI during the follicular and luteal phases of the menstrual cycle. At each time, resting-state functional connectivity was evaluated both before and after participants performed an emotion regulation task. The ECN was identified using independent components analysis, and connectivity of left and right amygdala seeds was also evaluated. RESULTS: Nonparametric permutation testing identified a cluster in the left middle temporal gyrus (MTG) with significantly stronger connectivity to the left ECN in women with PMDD vs. controls in all four fMRI sessions. Women with PMDD exhibited no difference in functional connectivity between menstrual cycle phases. Amygdala connectivity did not differ between the groups but differed significantly with menstrual phase, with left amygdala connectivity to cingulate cortex being significantly stronger during the follicular vs. luteal phase. Right amygdala connectivity to the middle frontal gyrus was also stronger during the follicular vs. luteal phase, with no group differences. These findings suggest that women with PMDD have different intrinsic network dynamics in the left executive control network compared to healthy controls. Nature Publishing Group UK 2019-12-11 /pmc/articles/PMC6906514/ /pubmed/31827073 http://dx.doi.org/10.1038/s41398-019-0670-8 Text en © The Author(s) 2019 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
Petersen, Nicole
Ghahremani, Dara G.
Rapkin, Andrea J.
Berman, Steven M.
Wijker, Noor
Liang, Letty
London, Edythe D.
Resting-state functional connectivity in women with PMDD
title Resting-state functional connectivity in women with PMDD
title_full Resting-state functional connectivity in women with PMDD
title_fullStr Resting-state functional connectivity in women with PMDD
title_full_unstemmed Resting-state functional connectivity in women with PMDD
title_short Resting-state functional connectivity in women with PMDD
title_sort resting-state functional connectivity in women with pmdd
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906514/
https://www.ncbi.nlm.nih.gov/pubmed/31827073
http://dx.doi.org/10.1038/s41398-019-0670-8
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