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Fertility Preservation Using GnRH Agonists: Rationale, Possible Mechanisms, and Explanation of Controversy
The only clinically accepted method of fertility preservation in young women facing gonadotoxic chemo- and/or radiotherapy for malignant or autoimmune diseases is cryopreservation of embryos or unfertilized ova, whereas cryopreservation of ovarian tissue for future reimplantation, or in vitro matura...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710670/ https://www.ncbi.nlm.nih.gov/pubmed/31488958 http://dx.doi.org/10.1177/1179558119870163 |
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author | Blumenfeld, Zeev |
author_facet | Blumenfeld, Zeev |
author_sort | Blumenfeld, Zeev |
collection | PubMed |
description | The only clinically accepted method of fertility preservation in young women facing gonadotoxic chemo- and/or radiotherapy for malignant or autoimmune diseases is cryopreservation of embryos or unfertilized ova, whereas cryopreservation of ovarian tissue for future reimplantation, or in vitro maturation of follicles, and the use of gonadotropin-releasing hormone agonists (GnRHa) are still considered investigational, by several authorities. Whereas previous publications have raised the fear of GnRHa’s possible detrimental effects in patients with hormone receptor-positive breast cancers, recent randomized controlled trials (RCTs) have shown that it either improves or does not affect disease-free survival (DFS) in such patients. This review summarizes the pros and cons of GnRHa co-treatment for fertility preservation, suggesting 5 theoretical mechanisms for GnRHa action: (1) simulating the prepubertal hypogonadotropic milieu, (2) direct effect on GnRH receptors, (3) decreased ovarian perfusion, (4) upregulation of an ovarian-protecting molecule such as sphingosine-1-phosphate, and (5) protecting a possible germinative stem cell. We try to explain the reasons for the discrepancy between most publications that support the use of GnRHa for fertility preservation and the minority of publications that did not support its efficiency. |
format | Online Article Text |
id | pubmed-6710670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67106702019-09-05 Fertility Preservation Using GnRH Agonists: Rationale, Possible Mechanisms, and Explanation of Controversy Blumenfeld, Zeev Clin Med Insights Reprod Health Fertility Preservation: Present Practice and Future Endeavors The only clinically accepted method of fertility preservation in young women facing gonadotoxic chemo- and/or radiotherapy for malignant or autoimmune diseases is cryopreservation of embryos or unfertilized ova, whereas cryopreservation of ovarian tissue for future reimplantation, or in vitro maturation of follicles, and the use of gonadotropin-releasing hormone agonists (GnRHa) are still considered investigational, by several authorities. Whereas previous publications have raised the fear of GnRHa’s possible detrimental effects in patients with hormone receptor-positive breast cancers, recent randomized controlled trials (RCTs) have shown that it either improves or does not affect disease-free survival (DFS) in such patients. This review summarizes the pros and cons of GnRHa co-treatment for fertility preservation, suggesting 5 theoretical mechanisms for GnRHa action: (1) simulating the prepubertal hypogonadotropic milieu, (2) direct effect on GnRH receptors, (3) decreased ovarian perfusion, (4) upregulation of an ovarian-protecting molecule such as sphingosine-1-phosphate, and (5) protecting a possible germinative stem cell. We try to explain the reasons for the discrepancy between most publications that support the use of GnRHa for fertility preservation and the minority of publications that did not support its efficiency. SAGE Publications 2019-08-21 /pmc/articles/PMC6710670/ /pubmed/31488958 http://dx.doi.org/10.1177/1179558119870163 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.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 | Fertility Preservation: Present Practice and Future Endeavors Blumenfeld, Zeev Fertility Preservation Using GnRH Agonists: Rationale, Possible Mechanisms, and Explanation of Controversy |
title | Fertility Preservation Using GnRH Agonists: Rationale, Possible Mechanisms, and Explanation of Controversy |
title_full | Fertility Preservation Using GnRH Agonists: Rationale, Possible Mechanisms, and Explanation of Controversy |
title_fullStr | Fertility Preservation Using GnRH Agonists: Rationale, Possible Mechanisms, and Explanation of Controversy |
title_full_unstemmed | Fertility Preservation Using GnRH Agonists: Rationale, Possible Mechanisms, and Explanation of Controversy |
title_short | Fertility Preservation Using GnRH Agonists: Rationale, Possible Mechanisms, and Explanation of Controversy |
title_sort | fertility preservation using gnrh agonists: rationale, possible mechanisms, and explanation of controversy |
topic | Fertility Preservation: Present Practice and Future Endeavors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710670/ https://www.ncbi.nlm.nih.gov/pubmed/31488958 http://dx.doi.org/10.1177/1179558119870163 |
work_keys_str_mv | AT blumenfeldzeev fertilitypreservationusinggnrhagonistsrationalepossiblemechanismsandexplanationofcontroversy |