Search for other papers by I Robertson in
Google Scholar
PubMed
Search for other papers by A J Kermack in
Google Scholar
PubMed
Complete Fertility, Princess Anne Hospital, Southampton, UK
Search for other papers by Y Cheong in
Google Scholar
PubMed
the European Society of Human Reproduction and Embryology (ESHRE), the American Society of Reproductive Medicine (ASRM) and the British Fertility Society (BFS) advocated a precautionary approach, advising infertility patients planning treatment to
Search for other papers by Meaghan J Griffiths in
Google Scholar
PubMed
Search for other papers by Lauren R Alesi in
Google Scholar
PubMed
Search for other papers by Amy L Winship in
Google Scholar
PubMed
Search for other papers by Karla J Hutt in
Google Scholar
PubMed
Graphical abstract
A mouse model to study uterine specific contributions to pregnancy.
Maternal environmental exposures can exert impacts on the ability of the uterus to sustain healthy pregnancy. To establish an in vivo model to study this, we designed an ovariectomized mouse embryo transfer model. The rationale being future studies could expose recipient female mice to variables such as altered diet, drug, temperature, air, or activity exposure among others to define their impacts on the uterine contribution to pregnancy. Ovariectomy ensures the extent of the variable is limited to exploring outcomes on uterine but not ovarian function. Embryo transfer from healthy, unexposed donor mice guarantees that any impacts of the variable are attributed to the maternal uterine but not the embryonic state. Pregnancy outcomes including pregnancy success (number of implantation sites) and viability (number of viable vs resorbing implantation sites) can be investigated. Numerous functional outcomes can be assessed, including developmental competence encompassing decidual, placental, fetal, and vascular morphology and/or function (e.g. measured using Doppler ultrasound, comparisons of fetal growth, or molecular or histological characterization of the decidua, placenta, and fetal tissues).
Lay summary
Many pregnancy complications occur because of problems in the womb (uterus), specifically the womb lining. There is a close relationship between the hormone function of the ovaries and the uterus and distinguishing between the way they both impact pregnancy success is difficult in existing studies using animals. Here, we developed a new animal model to utilize in addressing these gaps in our understanding of pregnancy.
Search for other papers by Roseanne Rosario in
Google Scholar
PubMed
The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia
Search for other papers by Wanyuan Cui in
Google Scholar
PubMed
Search for other papers by Richard A Anderson in
Google Scholar
PubMed
negative mTOR regulators Tsc1 ( Adhikari et al. 2010 ) and Tsc2 ( Adhikari et al. 2009 ) led to overactivation of primordial follicles and subsequent infertility, though interestingly, mTOR itself may not be necessary for primordial follicle
Search for other papers by Peter H Vogt in
Google Scholar
PubMed
Search for other papers by Jutta Zimmer in
Google Scholar
PubMed
Search for other papers by Ulrike Bender in
Google Scholar
PubMed
Search for other papers by Thomas Strowitzki in
Google Scholar
PubMed
. 2007 ). AZFa has a genomic extension of 1.1 Mb and includes a microdeletion found as de novo mutation event in about 9% of infertile men with a severe testicular pathology including complete germ cell aplasia ( Kamp et al. 2001 ). AZFa is thus part
Department of Nutrition and Integrative Physiology, University of Utah College of Health, Salt Lake City, Utah, USA
Search for other papers by Synneva Hagen-Lillevik in
Google Scholar
PubMed
Search for other papers by John S Rushing in
Google Scholar
PubMed
Search for other papers by Leslie Appiah in
Google Scholar
PubMed
Department of Nutrition and Integrative Physiology, University of Utah College of Health, Salt Lake City, Utah, USA
Search for other papers by Nicola Longo in
Google Scholar
PubMed
Search for other papers by Ashley Andrews in
Google Scholar
PubMed
Department of Nutrition and Integrative Physiology, University of Utah College of Health, Salt Lake City, Utah, USA
Search for other papers by Kent Lai in
Google Scholar
PubMed
Search for other papers by Joshua Johnson in
Google Scholar
PubMed
). POI can lead to infertility, hypoestrogenism, as well as mental distress ( Nelson 2009 ). The hypoestrogenic environment resulting from POI can result in poor bone health with an increased risk of fracture ( Marino & Misra 2011 , Batey et al. 2013
Faculty of Medicine and Life Sciences, Hasselt University, Agoralaan, Diepenbeek, Belgium
Search for other papers by Willem Ombelet in
Google Scholar
PubMed
Search for other papers by Federica Lopes in
Google Scholar
PubMed
Introduction Infertility is one of the most common chronic diseases among people of childbearing age, affecting roughly 8% to 12% of reproductive-aged couples worldwide ( Boivin et al. 2007 ), with men and women contributing almost equally
Search for other papers by Carlos H Miyashira in
Google Scholar
PubMed
Search for other papers by Fernanda Reali Oliveira in
Google Scholar
PubMed
Gynecologic Division, BP – A Beneficencia Portuguesa de Sao Paulo, Sao Paulo, Sao Paulo, Brazil
Search for other papers by Marina Paula Andres in
Google Scholar
PubMed
Search for other papers by Julian A Gingold in
Google Scholar
PubMed
Gynecologic Division, BP – A Beneficencia Portuguesa de Sao Paulo, Sao Paulo, Sao Paulo, Brazil
Search for other papers by Mauricio Simões Abrão in
Google Scholar
PubMed
endometriosis 36.1 ± 5.6 Cervical canal (67), posterior fornix (65), eutopic endometrium (2) Microbiome Shotgun sequencing 36 controls: infertility, myomas, ovarian borderline tumor, and teratoma Hernandes et al. (2020) Case
Infertility and Reproduction Research Program, Hunter Medical Research Institute, New Lambton Heights, Newcastle, NSW, Australia
Search for other papers by Leah Calvert in
Google Scholar
PubMed
Infertility and Reproduction Research Program, Hunter Medical Research Institute, New Lambton Heights, Newcastle, NSW, Australia
Search for other papers by Jacinta H Martin in
Google Scholar
PubMed
Infertility and Reproduction Research Program, Hunter Medical Research Institute, New Lambton Heights, Newcastle, NSW, Australia
Search for other papers by Amanda L Anderson in
Google Scholar
PubMed
Infertility and Reproduction Research Program, Hunter Medical Research Institute, New Lambton Heights, Newcastle, NSW, Australia
Search for other papers by Ilana R Bernstein in
Google Scholar
PubMed
Infertility and Reproduction Research Program, Hunter Medical Research Institute, New Lambton Heights, Newcastle, NSW, Australia
Search for other papers by Nathan D Burke in
Google Scholar
PubMed
Infertility and Reproduction Research Program, Hunter Medical Research Institute, New Lambton Heights, Newcastle, NSW, Australia
Search for other papers by Geoffry N De Iuliis in
Google Scholar
PubMed
Search for other papers by Andrew L Eamens in
Google Scholar
PubMed
Cancer Signalling Research Group, School of Biomedical Sciences and Pharmacy, College of Health, Medicine and Wellbeing, University of Newcastle, Callaghan, NSW, Australia
Search for other papers by Matthew D Dun in
Google Scholar
PubMed
Priority Research Centre for Geotechnical Science and Engineering, University of Newcastle, Callaghan, NSW, Australia
Search for other papers by Brett D Turner in
Google Scholar
PubMed
Search for other papers by Shaun D Roman in
Google Scholar
PubMed
Search for other papers by Mark P Green in
Google Scholar
PubMed
Infertility and Reproduction Research Program, Hunter Medical Research Institute, New Lambton Heights, Newcastle, NSW, Australia
Search for other papers by Brett Nixon in
Google Scholar
PubMed
Perfluoroalkyl chemicals and male reproductive health: do PFOA and PFOS increase risk for male infertility? International Journal of Environmental Research and Public Health 18 3794 . ( https://doi.org/10.3390/ijerph18073794 ) Toft G Jönsson BAG Lindh CH
Technion-Israel Institute of Technology, The Ruth and Bruce Rappaport Faculty of Medicine, Haifa, Israel
Search for other papers by Samer Khoury in
Google Scholar
PubMed
Technion-Israel Institute of Technology, The Ruth and Bruce Rappaport Faculty of Medicine, Haifa, Israel
Search for other papers by Einav Kadour-Peero in
Google Scholar
PubMed
Technion-Israel Institute of Technology, The Ruth and Bruce Rappaport Faculty of Medicine, Haifa, Israel
Search for other papers by Ilan Calderon in
Google Scholar
PubMed
Purpose
To evaluate the association between a rise in serum luteinizing hormone (LH) levels during artificial frozen–thawed embryo transfer (FET) cycles and clinical pregnancy rate.
Methods
A retrospective cohort study of women undergoing artificial FET cycles. We compared cycles in which LH double itself from the early follicular phase and further (group A) to cycles without a rise in LH (group B). Endometrium preparation was achieved by administration of 2 mg three times per day estradiol valerate tablets. Embryo transfer (ET) was conducted after achieving endometrial thickness > 7 mm and vaginal progesterone was added according to the embryo’s age. A beta-hCG was measured 13–14 days after ET. Clinical pregnancy was diagnosed on transvaginal ultrasound.
Results
Data from 984-FET cycles were retrieved. LH, exogenous estradiol (E2), progesterone values, endometrial thickness, and pregnancy outcomes were available in all patients. From 984-FET cycles, 629 (63.9%) had a doubling, and 355 (36.07%) had no rise in LH. Patients mean age was 30 years, similar in both groups. A multivariable logistic regression analysis was calculated to assess the effect of LH rise and pregnancy outcomes, after adjusting for confounders including a rise in E2 level and endometrial thickness. In this model, there was no association between doubling LH values and pregnancy rates (adjusted odds ratio: 1.06, 95% CI: 0.75–1.5, P = 0.74).
Conclusion
LH rise during artificial FET cycles does not alter pregnancy rates. Apparently, hormonal monitoring of LH levels may not yield useful information in the artificial FET cycle and may be omitted.
Lay summary
Supplementation of estradiol, a hormone produced by the ovaries, starting at the beginning of the menstrual cycle of an artificially frozen embryo transfer (FET) can lead to a rise in luteinizing hormone (LH), the hormone that induces ovulation. Such a rise in LH may interfere with embryo implantation, the process where the embryo attaches to the inner lining of the uterus and, therefore, could affect the chances of pregnancy. The current study is the first to assess the effect of a dynamic rise in LH levels during FET cycles on pregnancy rates. This study found no difference in pregnancy rates between FET cycles where the LH doubled compared to cycles without such a rise in LH. Larger, prospective studies should be conducted to assess the impact of LH elevation on pregnancy outcomes.
Search for other papers by Valéria Barradas in
Google Scholar
PubMed
Search for other papers by Mariana Pereira Antoniassi in
Google Scholar
PubMed
Search for other papers by Paula Intasqui in
Google Scholar
PubMed
Search for other papers by Marcilio Nichi in
Google Scholar
PubMed
Hospital São Paulo, São Paulo, Brazil
Search for other papers by Ricardo Pimenta Bertolla in
Google Scholar
PubMed
Search for other papers by Deborah Montagnini Spaine in
Google Scholar
PubMed
Introduction Infertility, defined as the couple's failure to conceive after 12 months of regular and unprotected sexual intercourse, affects about 15% of couples in reproductive age and the male factor is associated in up to 50% of cases