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The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders

OBJECTIVE: Follicular Output Rate (FORT) is an efficient quantitative and qualitative marker of ovarian responsiveness to gonadotropins. Transdermal testosterone (TT) has been used as adjuvant therapy to gonadotrophins in order to improve ovarian response in poor responders (PR). The aim of this stu...

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Autores principales: Solernou, Roser, Peralta, Sara, Casals, Gemma, Guimera, Marta, Solsona, Marina, Borras, Aina, Manau, Dolores, Fàbregues, Francesc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Society of Assisted Reproduction 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083864/
https://www.ncbi.nlm.nih.gov/pubmed/33507716
http://dx.doi.org/10.5935/1518-0557.20200086
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author Solernou, Roser
Peralta, Sara
Casals, Gemma
Guimera, Marta
Solsona, Marina
Borras, Aina
Manau, Dolores
Fàbregues, Francesc
author_facet Solernou, Roser
Peralta, Sara
Casals, Gemma
Guimera, Marta
Solsona, Marina
Borras, Aina
Manau, Dolores
Fàbregues, Francesc
author_sort Solernou, Roser
collection PubMed
description OBJECTIVE: Follicular Output Rate (FORT) is an efficient quantitative and qualitative marker of ovarian responsiveness to gonadotropins. Transdermal testosterone (TT) has been used as adjuvant therapy to gonadotrophins in order to improve ovarian response in poor responders (PR). The aim of this study was to analyze whether TT can improve follicular sensitivity to gonadotropins using FORT. METHODS: This retrospective study, held in a tertiary-care university hospital included 90 PR patients, according to the Bologna criteria. Patients in Group 1 (n = 46) received transdermal application of testosterone preceding gonadotrophin ovarian stimulation under pituitary suppression. In Group 2 (n = 44) ovarian stimulation was carried out with high-dose gonadotrophin in association with minidose GnRH agonist protocol. We analyzed ovarian stimulation parameters and IVF outcomes. We determined antral follicle count (AFC) (3-8 mm) before ovarian stimulation, pre-ovulatory follicle count (PFC) (16-22 mm) and the day of hCG administration. We calculated the FORT using the PFCx100/AFC ratio. RESULTS: Baseline characteristics and ovarian reserve parameters were similar in both groups. FORT and oocytes retrieved were significantly higher in group 1 vs group 2. There were no significant differences in pregnancy rates. In group 1 there was a significant correlation between FORT and AFC. CONCLUSIONS: This study suggests that the potential beneficial mechanism of TT in poor responder patients may be based on increasing the antral follicle sensitivity to gonadotrophin. FORT is an excellent tool to demonstrate this.
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spelling pubmed-80838642021-05-05 The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders Solernou, Roser Peralta, Sara Casals, Gemma Guimera, Marta Solsona, Marina Borras, Aina Manau, Dolores Fàbregues, Francesc JBRA Assist Reprod Original Article OBJECTIVE: Follicular Output Rate (FORT) is an efficient quantitative and qualitative marker of ovarian responsiveness to gonadotropins. Transdermal testosterone (TT) has been used as adjuvant therapy to gonadotrophins in order to improve ovarian response in poor responders (PR). The aim of this study was to analyze whether TT can improve follicular sensitivity to gonadotropins using FORT. METHODS: This retrospective study, held in a tertiary-care university hospital included 90 PR patients, according to the Bologna criteria. Patients in Group 1 (n = 46) received transdermal application of testosterone preceding gonadotrophin ovarian stimulation under pituitary suppression. In Group 2 (n = 44) ovarian stimulation was carried out with high-dose gonadotrophin in association with minidose GnRH agonist protocol. We analyzed ovarian stimulation parameters and IVF outcomes. We determined antral follicle count (AFC) (3-8 mm) before ovarian stimulation, pre-ovulatory follicle count (PFC) (16-22 mm) and the day of hCG administration. We calculated the FORT using the PFCx100/AFC ratio. RESULTS: Baseline characteristics and ovarian reserve parameters were similar in both groups. FORT and oocytes retrieved were significantly higher in group 1 vs group 2. There were no significant differences in pregnancy rates. In group 1 there was a significant correlation between FORT and AFC. CONCLUSIONS: This study suggests that the potential beneficial mechanism of TT in poor responder patients may be based on increasing the antral follicle sensitivity to gonadotrophin. FORT is an excellent tool to demonstrate this. Brazilian Society of Assisted Reproduction 2021 /pmc/articles/PMC8083864/ /pubmed/33507716 http://dx.doi.org/10.5935/1518-0557.20200086 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Solernou, Roser
Peralta, Sara
Casals, Gemma
Guimera, Marta
Solsona, Marina
Borras, Aina
Manau, Dolores
Fàbregues, Francesc
The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders
title The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders
title_full The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders
title_fullStr The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders
title_full_unstemmed The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders
title_short The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders
title_sort follicular output rate (fort) as a method to evaluate transdermal testosterone efficacy in poor responders
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083864/
https://www.ncbi.nlm.nih.gov/pubmed/33507716
http://dx.doi.org/10.5935/1518-0557.20200086
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