Progesterone rise on HCG day in GnRH antagonist/rFSH stimulated cycles affects endometrial gene expression

169Citations
Citations of this article
71Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Premature progesterone rise during gonadotrophin-releasing hormone (GnRH) antagonist cycles for IVF is a frequent phenomenon and has been associated with lower pregnancy and implantation rates. This study evaluated endometrial gene expression on the day of oocyte retrieval according to the concentration of serum progesterone on the day of human chorionic gonadotrophin (HCG) administration in GnRH-antagonist/recombinant FSH IVF cycles with fresh embryo transfer. Endometrial biopsies (n = 14) were analysed with Affymetrix HG U133 Plus 2.0 Arrays. Patients were divided into three groups according to their progesterone serum concentration on the day of HCG administration: ≤0.9 ng/ml (group A), 1-1.5 ng/ml (group B) and >1.5 ng/ml (group C). Gene expression analysis showed a small number of significantly differentially expressed probe sets between groups A and B (five up/23 down in B) and a large difference between groups B and C (607 up/212 down; P ≤ 0.05, fold change ≥1.4). Validation was performed with quantitative real-time PCR on selected genes. As far as is known, this is the first study to demonstrate a distinct difference in endometrial gene expression profile between patients with a progesterone serum concentration above and below the threshold of 1.5 ng/ml on the day of HCG administration. © 2010, Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.

Cite

CITATION STYLE

APA

Van Vaerenbergh, I., Fatemi, H. M., Blockeel, C., Van Lommel, L., In’T Veld, P., Schuit, F., … Bourgain, C. (2011). Progesterone rise on HCG day in GnRH antagonist/rFSH stimulated cycles affects endometrial gene expression. Reproductive BioMedicine Online, 22(3), 263–271. https://doi.org/10.1016/j.rbmo.2010.11.002

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free