Local production of 17β-oestradiol in the endometrium during the implantation window: a pilot study

Author:

Stevens Brentjens L B P M12ORCID,Obukhova D23,Delvoux B12,den Hartog J E12,Bui B N4,Mol F5,de Bruin J P6,Besselink D7,Teklenburg G8,Morgan F9,Baker M9,Broekmans F J M4,van Golde R J T12,Zamani Esteki M2310,Romano A12ORCID

Affiliation:

1. Department of Obstetrics and Gynaecology, Maastricht University Medical Centre+, Maastricht, The Netherlands

2. GROW School for Oncology and Reproduction, Maastricht University, Universiteitssingel, Maastricht, The Netherlands

3. Department of Clinical Genetics, Maastricht University Medical Centre (MUMC+), Maastricht, The Netherlands

4. Department of Gynaecology & Reproductive Medicine, University Medical Centre Utrecht, Heidelberglaan, Utrecht, The Netherlands

5. Centre for Reproductive Medicine, Reproduction and Development, Amsterdam University Medical Centre, University of Amsterdam, Meibergdreef, Amsterdam, The Netherlands

6. Department of Obstetrics and Gynaecology, Jeroen Bosch Hospital, Henri Dunantstraat, Hertogenbosch, The Netherlands

7. Department of Obstetrics and Gynaecology, Radboud University Medical Centre, Geert Grooteplein Zuid, Nijmegen, The Netherlands

8. Isala Fertility Clinic, Isala Hospital, Dokter van Heesweg, Zwolle, The Netherlands

9. Department of Complex Tissue Regeneration, MERLN Institute, Maastricht University, Maastricht, The Netherlands

10. Division of Obstetrics and Gynaecology, Department of Clinical Science, Intervention & Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden

Abstract

Graphical abstract Abstract Sex steroids are converted to bioactive metabolites and vice versa by endometrial steroid-metabolising enzymes. Studies indicate that alterations in this metabolism might affect endometrial receptivity. This pilot study determined whether the endometrial formation and inactivation of 17β-oestradiol differed between the supposedly embryo-receptive endometrium and non-receptive endometrium of women undergoing IVF/intracytoplasmic sperm injection (ICSI). Endometrial biopsies were obtained from IVF/ICSI patients 5–8 days after ovulation in a natural cycle, prior to their second IVF/ICSI cycle with fresh embryo transfer (ET). Endometrial biopsies from patients who achieved clinical pregnancy after fresh ET (n = 15) were compared with endometrial biopsies from patients that did not conceive after fresh ET (n = 15). Formation of 17β-oestradiol (oxidative 17β-hydroxysteroid dehydrogenases (HSDs)), oestrone (reductive HSD17Bs) and inhibition of HSD17B1 activity were determined by high-performance liquid chromatography. The endometrial transcriptome was profiled using RNA sequencing followed by principal component analysis and differentially expressed gene analysis. The false discovery rate-adjusted P < 0.05 and log fold change >0.5 were selected as the screening threshold. Formation and inactivation of 17β-oestradiol resulted similar between groups. Inhibition of HSD17B1 activity was significantly higher in the non-pregnant group when only primary infertile women (n = 12) were considered (27.1%, n = 5 vs 16.2%, n = 7, P = 0.04). Gene expression analysis confirmed the presence of HSD17B1 (encoding HSD17B1), HSD17B2 (encoding HSD17B2) and 33 of 46 analysed steroid metabolising enzymes in the endometrium. In the primary infertile subgroup (n = 10) 12 DEGs were found including LINC02349 which has been linked to implantation. However, the exact relationship between steroid-metabolising enzyme activity, expression and implantation outcome requires further investigation in larger, well-defined patient groups. Lay summary Sex hormones are produced and broken down by enzymes that can be found in the endometrium (the inner lining of the womb). This enzyme activity might influence the chances of becoming pregnant. We compared (i) enzyme activity in the endometrium of 15 women who did and 15 women who did not become pregnant in their second in vitro fertilisation attempt, (ii) how enzyme activity can be blocked by an inhibitor, and (iii) differences in gene expression (the process by which instructions in our DNA are converted into a product). Enzyme activity was similar between groups. We found that in women who have never been pregnant in the past, inhibition of enzyme activity was higher and found differences in a gene that has been linked to the implantation of the embryo, but future studies should be performed in larger, well-defined patient groups to confirm these findings.

Publisher

Bioscientifica

Subject

Urology,Reproductive Medicine,Obstetrics and Gynecology,Embryology

Reference29 articles.

1. The endometrial microbiota of women with or without a live birth within 12 months after a first failed IVF/ICSI cycle;Bui,2023

2. De novo synthesis of estrogen in pregnant uterus is critical for stromal decidualization and angiogenesis;Das,2009

3. A sensitive HPLC method for the assessment of metabolic conversion of estrogens;Delvoux,2007

4. Increased production of 17beta-estradiol in endometriosis lesions is the result of impaired metabolism;Delvoux,2009

5. Inhibition of type 1 17beta-hydroxysteroid dehydrogenase impairs the synthesis of 17beta-estradiol in endometriosis lesions;Delvoux,2014

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