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Endometrial Receptivity Profile in Patients with Premature Progesterone Elevation on the Day of hCG Administration
The impact of a premature elevation of serum progesterone level, the day of hCG administration in patients under controlled ovarian stimulation during IVF procedure, on human endometrial receptivity is still debated. In the present study, we investigated the endometrial gene expression profile shift...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022194/ https://www.ncbi.nlm.nih.gov/pubmed/24877150 http://dx.doi.org/10.1155/2014/951937 |
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author | Haouzi, Delphine Bissonnette, Laurence Gala, Anna Assou, Said Entezami, Frida Perrochia, Hélène Dechaud, Hervé Hugues, Jean-Noel Hamamah, Samir |
author_facet | Haouzi, Delphine Bissonnette, Laurence Gala, Anna Assou, Said Entezami, Frida Perrochia, Hélène Dechaud, Hervé Hugues, Jean-Noel Hamamah, Samir |
author_sort | Haouzi, Delphine |
collection | PubMed |
description | The impact of a premature elevation of serum progesterone level, the day of hCG administration in patients under controlled ovarian stimulation during IVF procedure, on human endometrial receptivity is still debated. In the present study, we investigated the endometrial gene expression profile shifts during the prereceptive and receptive secretory stage in patients with normal and elevated serum progesterone level on the day of hCG administration in fifteen patients under stimulated cycles. Then, specific biomarkers of endometrial receptivity in these two groups of patients were tested. Endometrial biopsies were performed on oocyte retrieval day and on day 3 of embryo transfer, respectively, for each patient. Samples were analysed using DNA microarrays and qRT-PCR. The endometrial gene expression shift from the prereceptive to the receptive stage was altered in patients with high serum progesterone level (>1.5 ng/mL) on hCG day, suggesting accelerated endometrial maturation during the periovulation period. This was confirmed by the functional annotation of the differentially expressed genes as it showed downregulation of cell cycle-related genes. Conversely, the profile of endometrial receptivity was comparable in both groups. Premature progesterone rise alters the endometrial gene expression shift between the prereceptive and the receptive stage but does not affect endometrial receptivity. |
format | Online Article Text |
id | pubmed-4022194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40221942014-05-29 Endometrial Receptivity Profile in Patients with Premature Progesterone Elevation on the Day of hCG Administration Haouzi, Delphine Bissonnette, Laurence Gala, Anna Assou, Said Entezami, Frida Perrochia, Hélène Dechaud, Hervé Hugues, Jean-Noel Hamamah, Samir Biomed Res Int Research Article The impact of a premature elevation of serum progesterone level, the day of hCG administration in patients under controlled ovarian stimulation during IVF procedure, on human endometrial receptivity is still debated. In the present study, we investigated the endometrial gene expression profile shifts during the prereceptive and receptive secretory stage in patients with normal and elevated serum progesterone level on the day of hCG administration in fifteen patients under stimulated cycles. Then, specific biomarkers of endometrial receptivity in these two groups of patients were tested. Endometrial biopsies were performed on oocyte retrieval day and on day 3 of embryo transfer, respectively, for each patient. Samples were analysed using DNA microarrays and qRT-PCR. The endometrial gene expression shift from the prereceptive to the receptive stage was altered in patients with high serum progesterone level (>1.5 ng/mL) on hCG day, suggesting accelerated endometrial maturation during the periovulation period. This was confirmed by the functional annotation of the differentially expressed genes as it showed downregulation of cell cycle-related genes. Conversely, the profile of endometrial receptivity was comparable in both groups. Premature progesterone rise alters the endometrial gene expression shift between the prereceptive and the receptive stage but does not affect endometrial receptivity. Hindawi Publishing Corporation 2014 2014-04-28 /pmc/articles/PMC4022194/ /pubmed/24877150 http://dx.doi.org/10.1155/2014/951937 Text en Copyright © 2014 Delphine Haouzi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Haouzi, Delphine Bissonnette, Laurence Gala, Anna Assou, Said Entezami, Frida Perrochia, Hélène Dechaud, Hervé Hugues, Jean-Noel Hamamah, Samir Endometrial Receptivity Profile in Patients with Premature Progesterone Elevation on the Day of hCG Administration |
title | Endometrial Receptivity Profile in Patients with Premature Progesterone Elevation on the Day of hCG Administration |
title_full | Endometrial Receptivity Profile in Patients with Premature Progesterone Elevation on the Day of hCG Administration |
title_fullStr | Endometrial Receptivity Profile in Patients with Premature Progesterone Elevation on the Day of hCG Administration |
title_full_unstemmed | Endometrial Receptivity Profile in Patients with Premature Progesterone Elevation on the Day of hCG Administration |
title_short | Endometrial Receptivity Profile in Patients with Premature Progesterone Elevation on the Day of hCG Administration |
title_sort | endometrial receptivity profile in patients with premature progesterone elevation on the day of hcg administration |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022194/ https://www.ncbi.nlm.nih.gov/pubmed/24877150 http://dx.doi.org/10.1155/2014/951937 |
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