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Defining ovarian reserve to better understand ovarian aging
Though a widely utilized term and clinical concept, ovarian reserve (OR) has been only inadequately defined. Based on Medline and PubMed searches we here define OR in its various components, review genetic control of OR, with special emphasis on the FMR1 gene, and discuss whether diminished OR (DOR)...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042920/ https://www.ncbi.nlm.nih.gov/pubmed/21299886 http://dx.doi.org/10.1186/1477-7827-9-23 |
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author | Gleicher, Norbert Weghofer, Andrea Barad, David H |
author_facet | Gleicher, Norbert Weghofer, Andrea Barad, David H |
author_sort | Gleicher, Norbert |
collection | PubMed |
description | Though a widely utilized term and clinical concept, ovarian reserve (OR) has been only inadequately defined. Based on Medline and PubMed searches we here define OR in its various components, review genetic control of OR, with special emphasis on the FMR1 gene, and discuss whether diminished OR (DOR) is treatable. What is generally referred to as OR reflects only a small portion of total OR (TOR), a pool of growing (recruited) follicles (GFs) at different stages of maturation. Functional OR (FOR) depends on size of the follicle pool at menarche and the follicle recruitment rate. Both vary between individuals and, at least partially, are under genetic control. The FMR1 gene plays a role in defining FOR at all ages. Infertility treatments have in the past almost exclusively only centered on the last two weeks of folliculogenesis, the gonadotropin-sensitive phase. Expansions of treatments into earlier stages of maturation will offer opportunity to significantly improve ovarian stimulation protocols, especially in women with DOR. Dehydroepiandrosterone (DHEA) may represent a first such intervention. Data generated in DHEA-supplemented women, indeed, suggest a new ovarian aging concept, based on aging of ovarian environments and not, as currently is believed, aging oocytes. |
format | Text |
id | pubmed-3042920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30429202011-02-23 Defining ovarian reserve to better understand ovarian aging Gleicher, Norbert Weghofer, Andrea Barad, David H Reprod Biol Endocrinol Review Though a widely utilized term and clinical concept, ovarian reserve (OR) has been only inadequately defined. Based on Medline and PubMed searches we here define OR in its various components, review genetic control of OR, with special emphasis on the FMR1 gene, and discuss whether diminished OR (DOR) is treatable. What is generally referred to as OR reflects only a small portion of total OR (TOR), a pool of growing (recruited) follicles (GFs) at different stages of maturation. Functional OR (FOR) depends on size of the follicle pool at menarche and the follicle recruitment rate. Both vary between individuals and, at least partially, are under genetic control. The FMR1 gene plays a role in defining FOR at all ages. Infertility treatments have in the past almost exclusively only centered on the last two weeks of folliculogenesis, the gonadotropin-sensitive phase. Expansions of treatments into earlier stages of maturation will offer opportunity to significantly improve ovarian stimulation protocols, especially in women with DOR. Dehydroepiandrosterone (DHEA) may represent a first such intervention. Data generated in DHEA-supplemented women, indeed, suggest a new ovarian aging concept, based on aging of ovarian environments and not, as currently is believed, aging oocytes. BioMed Central 2011-02-07 /pmc/articles/PMC3042920/ /pubmed/21299886 http://dx.doi.org/10.1186/1477-7827-9-23 Text en Copyright ©2011 Gleicher et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Gleicher, Norbert Weghofer, Andrea Barad, David H Defining ovarian reserve to better understand ovarian aging |
title | Defining ovarian reserve to better understand ovarian aging |
title_full | Defining ovarian reserve to better understand ovarian aging |
title_fullStr | Defining ovarian reserve to better understand ovarian aging |
title_full_unstemmed | Defining ovarian reserve to better understand ovarian aging |
title_short | Defining ovarian reserve to better understand ovarian aging |
title_sort | defining ovarian reserve to better understand ovarian aging |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042920/ https://www.ncbi.nlm.nih.gov/pubmed/21299886 http://dx.doi.org/10.1186/1477-7827-9-23 |
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