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Persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea

Menstrual pain, also known as dysmenorrhea, is a leading risk factor for bladder pain syndrome (BPS). A better understanding of the mechanisms that predispose dysmenorrheic women to BPS is needed to develop prophylactic strategies. Abnormal autonomic regulation, a key factor implicated in BPS and ch...

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Autores principales: Oladosu, Folabomi A., Hellman, Kevin M., Ham, Paula J., Kochlefl, Laura E., Datta, Avisek, Garrison, Ellen F., Steiner, Nicole D., Roth, Genevieve E., Tu, Frank F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379479/
https://www.ncbi.nlm.nih.gov/pubmed/30778114
http://dx.doi.org/10.1038/s41598-019-38545-3
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author Oladosu, Folabomi A.
Hellman, Kevin M.
Ham, Paula J.
Kochlefl, Laura E.
Datta, Avisek
Garrison, Ellen F.
Steiner, Nicole D.
Roth, Genevieve E.
Tu, Frank F.
author_facet Oladosu, Folabomi A.
Hellman, Kevin M.
Ham, Paula J.
Kochlefl, Laura E.
Datta, Avisek
Garrison, Ellen F.
Steiner, Nicole D.
Roth, Genevieve E.
Tu, Frank F.
author_sort Oladosu, Folabomi A.
collection PubMed
description Menstrual pain, also known as dysmenorrhea, is a leading risk factor for bladder pain syndrome (BPS). A better understanding of the mechanisms that predispose dysmenorrheic women to BPS is needed to develop prophylactic strategies. Abnormal autonomic regulation, a key factor implicated in BPS and chronic pain, has not been adequately characterized in women with dysmenorrhea. Thus, we examined heart rate variability (HRV) in healthy (n = 34), dysmenorrheic (n = 103), and BPS participants (n = 23) in their luteal phase across a bladder-filling task. Both dysmenorrheic and BPS participants reported increased bladder pain sensitivity when compared to controls (p’s < 0.001). Similarly, dysmenorrheic and BPS participants had increased heart rate (p’s < 0.01), increased diastolic blood pressure (p’s < 0.01), and reduced HRV (p’s < 0.05) when compared to controls. Dysmenorrheic participants also exhibited little change in heart rate between maximum bladder capacity and after micturition when compared to controls (p = 0.013). Our findings demonstrate menstrual pain’s association with abnormal autonomic activity and bladder sensitivity, even two weeks after menses. Our findings of autonomic dysfunction in both early episodic and chronic visceral pain states points to an urgent need to elucidate the development of such imbalance, perhaps beginning in adolescence.
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spelling pubmed-63794792019-02-21 Persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea Oladosu, Folabomi A. Hellman, Kevin M. Ham, Paula J. Kochlefl, Laura E. Datta, Avisek Garrison, Ellen F. Steiner, Nicole D. Roth, Genevieve E. Tu, Frank F. Sci Rep Article Menstrual pain, also known as dysmenorrhea, is a leading risk factor for bladder pain syndrome (BPS). A better understanding of the mechanisms that predispose dysmenorrheic women to BPS is needed to develop prophylactic strategies. Abnormal autonomic regulation, a key factor implicated in BPS and chronic pain, has not been adequately characterized in women with dysmenorrhea. Thus, we examined heart rate variability (HRV) in healthy (n = 34), dysmenorrheic (n = 103), and BPS participants (n = 23) in their luteal phase across a bladder-filling task. Both dysmenorrheic and BPS participants reported increased bladder pain sensitivity when compared to controls (p’s < 0.001). Similarly, dysmenorrheic and BPS participants had increased heart rate (p’s < 0.01), increased diastolic blood pressure (p’s < 0.01), and reduced HRV (p’s < 0.05) when compared to controls. Dysmenorrheic participants also exhibited little change in heart rate between maximum bladder capacity and after micturition when compared to controls (p = 0.013). Our findings demonstrate menstrual pain’s association with abnormal autonomic activity and bladder sensitivity, even two weeks after menses. Our findings of autonomic dysfunction in both early episodic and chronic visceral pain states points to an urgent need to elucidate the development of such imbalance, perhaps beginning in adolescence. Nature Publishing Group UK 2019-02-18 /pmc/articles/PMC6379479/ /pubmed/30778114 http://dx.doi.org/10.1038/s41598-019-38545-3 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
Oladosu, Folabomi A.
Hellman, Kevin M.
Ham, Paula J.
Kochlefl, Laura E.
Datta, Avisek
Garrison, Ellen F.
Steiner, Nicole D.
Roth, Genevieve E.
Tu, Frank F.
Persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea
title Persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea
title_full Persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea
title_fullStr Persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea
title_full_unstemmed Persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea
title_short Persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea
title_sort persistent autonomic dysfunction and bladder sensitivity in primary dysmenorrhea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379479/
https://www.ncbi.nlm.nih.gov/pubmed/30778114
http://dx.doi.org/10.1038/s41598-019-38545-3
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