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Dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type

Administration of Dienogest prior to hysteroscopic polypectomy is empirically performed, but the physiological effects of Dienogest on endometrial polyps are unclear. We aimed to investigate the effects of Dienogest on the proliferation and inflammation of endometrial polyps. We conducted a retrospe...

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Autores principales: Inaba, Kei, Wada-Hiraike, Osamu, Harada, Miyuki, Hirota, Yasushi, Koga, Kaori, Fujii, Tomoyuki, Osuga, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448127/
https://www.ncbi.nlm.nih.gov/pubmed/32833600
http://dx.doi.org/10.1177/1745506520952003
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author Inaba, Kei
Wada-Hiraike, Osamu
Harada, Miyuki
Hirota, Yasushi
Koga, Kaori
Fujii, Tomoyuki
Osuga, Yutaka
author_facet Inaba, Kei
Wada-Hiraike, Osamu
Harada, Miyuki
Hirota, Yasushi
Koga, Kaori
Fujii, Tomoyuki
Osuga, Yutaka
author_sort Inaba, Kei
collection PubMed
description Administration of Dienogest prior to hysteroscopic polypectomy is empirically performed, but the physiological effects of Dienogest on endometrial polyps are unclear. We aimed to investigate the effects of Dienogest on the proliferation and inflammation of endometrial polyps. We conducted a retrospective case study on 40 menstruating women who underwent hysteroscopic polypectomy at our hospital. We collected clinical data, and the polyps were divided by morphological appearance. The specimens obtained were immunostained for Ki67 as a marker of cellar proliferation and CD138 as a marker of plasmacytes, which are a hallmark of chronic endometritis. Dienogest significantly suppressed the proliferation status of EPs because Dienogest treatment prior to the operation significantly reduced the Ki67 index (41.25 ± 16.85 vs 7.18 ± 9.82, p < 0.01). We found that sessile-type polyps showed a significantly lower Ki67 index than the pedunculated type (12.28 ± 11.12 vs 2.09 ± 2.73, p = 0.026). The presence of CD138-positive cells was more pronounced in sessile-type polyps than in pedunculated polyps (p = 0.018). However, Dienogest treatment showed no apparent effect on inflammation status, as detected by CD138-positive cells. We revealed that Dienogest suppressed cellular proliferation, and morphological classification of endometrial polyps could be used to predict the responsiveness to Dienogest. However, Dienogest might not affect cellular inflammation.
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spelling pubmed-74481272020-09-10 Dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type Inaba, Kei Wada-Hiraike, Osamu Harada, Miyuki Hirota, Yasushi Koga, Kaori Fujii, Tomoyuki Osuga, Yutaka Womens Health (Lond) Short Communication Administration of Dienogest prior to hysteroscopic polypectomy is empirically performed, but the physiological effects of Dienogest on endometrial polyps are unclear. We aimed to investigate the effects of Dienogest on the proliferation and inflammation of endometrial polyps. We conducted a retrospective case study on 40 menstruating women who underwent hysteroscopic polypectomy at our hospital. We collected clinical data, and the polyps were divided by morphological appearance. The specimens obtained were immunostained for Ki67 as a marker of cellar proliferation and CD138 as a marker of plasmacytes, which are a hallmark of chronic endometritis. Dienogest significantly suppressed the proliferation status of EPs because Dienogest treatment prior to the operation significantly reduced the Ki67 index (41.25 ± 16.85 vs 7.18 ± 9.82, p < 0.01). We found that sessile-type polyps showed a significantly lower Ki67 index than the pedunculated type (12.28 ± 11.12 vs 2.09 ± 2.73, p = 0.026). The presence of CD138-positive cells was more pronounced in sessile-type polyps than in pedunculated polyps (p = 0.018). However, Dienogest treatment showed no apparent effect on inflammation status, as detected by CD138-positive cells. We revealed that Dienogest suppressed cellular proliferation, and morphological classification of endometrial polyps could be used to predict the responsiveness to Dienogest. However, Dienogest might not affect cellular inflammation. SAGE Publications 2020-08-24 /pmc/articles/PMC7448127/ /pubmed/32833600 http://dx.doi.org/10.1177/1745506520952003 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Short Communication
Inaba, Kei
Wada-Hiraike, Osamu
Harada, Miyuki
Hirota, Yasushi
Koga, Kaori
Fujii, Tomoyuki
Osuga, Yutaka
Dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type
title Dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type
title_full Dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type
title_fullStr Dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type
title_full_unstemmed Dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type
title_short Dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type
title_sort dienogest suppresses cellular proliferation status of endometrial polyps and acts differently depending on the morphological type
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448127/
https://www.ncbi.nlm.nih.gov/pubmed/32833600
http://dx.doi.org/10.1177/1745506520952003
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