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MON-LB9 Cyclic Progesterone Therapy in Androgenic Polycystic Ovary Syndrome (PCOS) - Person-Related 6-Month Experience Changes

Endometrial cancer(1) and oligomenorrhea(2) are common risks for women living with androgenic PCOS (WLWP); cyclic progesterone therapy could prevent both. Cyclic oral micronized progesterone therapy (Cyclic OMP; 300 mg at hs/14 days/cycle) also corrects the neuroendocrine origins of PCOS(3). Althoug...

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Autores principales: Shirin, Sonia, Murray, Faye, Hajjaran, Maryam, Goshtasebi, Azita, Kalidasan, Dharani, Prior, Jerilynn C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208794/
http://dx.doi.org/10.1210/jendso/bvaa046.2332
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author Shirin, Sonia
Murray, Faye
Hajjaran, Maryam
Goshtasebi, Azita
Kalidasan, Dharani
Prior, Jerilynn C
author_facet Shirin, Sonia
Murray, Faye
Hajjaran, Maryam
Goshtasebi, Azita
Kalidasan, Dharani
Prior, Jerilynn C
author_sort Shirin, Sonia
collection PubMed
description Endometrial cancer(1) and oligomenorrhea(2) are common risks for women living with androgenic PCOS (WLWP); cyclic progesterone therapy could prevent both. Cyclic oral micronized progesterone therapy (Cyclic OMP; 300 mg at hs/14 days/cycle) also corrects the neuroendocrine origins of PCOS(3). Although vaginal progesterone is used in PCOS ovulation induction (4), and short Cyclic OMP decreases LH and/or Testosterone (5,6), no WLWP person-level prospective data with Cyclic OMP therapy are published. A WLWP, aged 31, BMI 20.1, with heavy flow and slightly irregular ~35-day cycles, was unable to tolerate birth control pills. She was prescribed Cyclic OMP (300 mg/h.s. cycle days 14-27)(7). She began keeping the Menstrual Cycle Diary© (Diary), a 19-item tool (scored 0-4), during her 1(st) Cyclic OMP cycle and took no other therapy. This pilot study was designed to understand Cyclic OMP-related experience changes in WLWP: 1) by documenting experience changes on the 1(st) to the 6(th) complete Diary; and 2) by assessing follicular phase changes in baseline data (no Rx) vs. cycles 3 and 6. We entered data from six consecutive Diaries into an SPSS (Version 24) database. Analysis #1 used Wilcoxon Signed Ranks Tests (for within-person ordinal data) and #2 repeated measures ANOVA. Research question: What Cyclic OMP-related experience changes occurred for a WLWP? On Cyclic OMP, she spontaneously reported improvements in aching joints, sleep and GI problems. We assessed selected, potentially E2-related Diary changes: flow, fluid retention, breast tenderness, stretchy cervical mucus and anxiety. Cyclic OMP was associated with shorter cycle lengths of 28.17+/-0.8 days. Fluid retention (P=0.000), mucus (P=0.048), and breast tenderness (P=0.000) all decreased, but anxiety and flow were unchanged. Follicular phase only fluid retention significantly decreased (F (1.2, 14.7) = 6.7, P =0.017). Although open-label, these prospective analyses suggest that Cyclic OMP, alone, is related to short-term benefits in androgenic PCOS. Prospective studies and controlled comparative trials of this innovative “luteal phase replacement” PCOS therapy are needed. Reference:(1)Barry J Hum Reprod Update 2014 20:748. (2)Azziz R Nat Rev Dis Primers 2016;2:16057. (3)Blank S Hum Reprod Update 2006;12:351. (4)Montville C Fertil Steril 2010;94:678. (5)Livadas S Fertil Steril 2010;94:242. (6)Bagis T J Clin Endocr Met 2002;87:4536. (7)Prior J https://hellocluecom/articles/cycle-a-z/the-case-for-a-new-pcos-therapy 2018
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spelling pubmed-72087942020-05-13 MON-LB9 Cyclic Progesterone Therapy in Androgenic Polycystic Ovary Syndrome (PCOS) - Person-Related 6-Month Experience Changes Shirin, Sonia Murray, Faye Hajjaran, Maryam Goshtasebi, Azita Kalidasan, Dharani Prior, Jerilynn C J Endocr Soc Reproductive Endocrinology Endometrial cancer(1) and oligomenorrhea(2) are common risks for women living with androgenic PCOS (WLWP); cyclic progesterone therapy could prevent both. Cyclic oral micronized progesterone therapy (Cyclic OMP; 300 mg at hs/14 days/cycle) also corrects the neuroendocrine origins of PCOS(3). Although vaginal progesterone is used in PCOS ovulation induction (4), and short Cyclic OMP decreases LH and/or Testosterone (5,6), no WLWP person-level prospective data with Cyclic OMP therapy are published. A WLWP, aged 31, BMI 20.1, with heavy flow and slightly irregular ~35-day cycles, was unable to tolerate birth control pills. She was prescribed Cyclic OMP (300 mg/h.s. cycle days 14-27)(7). She began keeping the Menstrual Cycle Diary© (Diary), a 19-item tool (scored 0-4), during her 1(st) Cyclic OMP cycle and took no other therapy. This pilot study was designed to understand Cyclic OMP-related experience changes in WLWP: 1) by documenting experience changes on the 1(st) to the 6(th) complete Diary; and 2) by assessing follicular phase changes in baseline data (no Rx) vs. cycles 3 and 6. We entered data from six consecutive Diaries into an SPSS (Version 24) database. Analysis #1 used Wilcoxon Signed Ranks Tests (for within-person ordinal data) and #2 repeated measures ANOVA. Research question: What Cyclic OMP-related experience changes occurred for a WLWP? On Cyclic OMP, she spontaneously reported improvements in aching joints, sleep and GI problems. We assessed selected, potentially E2-related Diary changes: flow, fluid retention, breast tenderness, stretchy cervical mucus and anxiety. Cyclic OMP was associated with shorter cycle lengths of 28.17+/-0.8 days. Fluid retention (P=0.000), mucus (P=0.048), and breast tenderness (P=0.000) all decreased, but anxiety and flow were unchanged. Follicular phase only fluid retention significantly decreased (F (1.2, 14.7) = 6.7, P =0.017). Although open-label, these prospective analyses suggest that Cyclic OMP, alone, is related to short-term benefits in androgenic PCOS. Prospective studies and controlled comparative trials of this innovative “luteal phase replacement” PCOS therapy are needed. Reference:(1)Barry J Hum Reprod Update 2014 20:748. (2)Azziz R Nat Rev Dis Primers 2016;2:16057. (3)Blank S Hum Reprod Update 2006;12:351. (4)Montville C Fertil Steril 2010;94:678. (5)Livadas S Fertil Steril 2010;94:242. (6)Bagis T J Clin Endocr Met 2002;87:4536. (7)Prior J https://hellocluecom/articles/cycle-a-z/the-case-for-a-new-pcos-therapy 2018 Oxford University Press 2020-05-08 /pmc/articles/PMC7208794/ http://dx.doi.org/10.1210/jendso/bvaa046.2332 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Reproductive Endocrinology
Shirin, Sonia
Murray, Faye
Hajjaran, Maryam
Goshtasebi, Azita
Kalidasan, Dharani
Prior, Jerilynn C
MON-LB9 Cyclic Progesterone Therapy in Androgenic Polycystic Ovary Syndrome (PCOS) - Person-Related 6-Month Experience Changes
title MON-LB9 Cyclic Progesterone Therapy in Androgenic Polycystic Ovary Syndrome (PCOS) - Person-Related 6-Month Experience Changes
title_full MON-LB9 Cyclic Progesterone Therapy in Androgenic Polycystic Ovary Syndrome (PCOS) - Person-Related 6-Month Experience Changes
title_fullStr MON-LB9 Cyclic Progesterone Therapy in Androgenic Polycystic Ovary Syndrome (PCOS) - Person-Related 6-Month Experience Changes
title_full_unstemmed MON-LB9 Cyclic Progesterone Therapy in Androgenic Polycystic Ovary Syndrome (PCOS) - Person-Related 6-Month Experience Changes
title_short MON-LB9 Cyclic Progesterone Therapy in Androgenic Polycystic Ovary Syndrome (PCOS) - Person-Related 6-Month Experience Changes
title_sort mon-lb9 cyclic progesterone therapy in androgenic polycystic ovary syndrome (pcos) - person-related 6-month experience changes
topic Reproductive Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208794/
http://dx.doi.org/10.1210/jendso/bvaa046.2332
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