Abstract
Purpose
This work aimed to study clinical and neonatal outcomes of embryos derived from frozen compared to fresh donor oocytes in gestational carrier cycles.
Methods
This is a retrospective cohort study using the Society for Assisted Reproductive Technology Clinic Outcome Reporting System database between 2014 and 2015, comprising of 1284 fresh transfer cycles to gestational carrier recipients of embryos resulting from fresh (n = 1119) and vitrified/thawed (n = 165) donor oocytes. Models were adjusted for gestational carrier age, preimplantation genetic testing (PGT-A), number of embryos transferred, multiple gestation, and fetal heart reduction. As our models were part of a larger analysis, intended parent BMI, smoking status, and parity were also adjusted for, but did not influence outcomes in this analysis.
Results
There was no significant difference in probability of live birth rates when comparing embryos derived from fresh and frozen donor oocytes in gestational carrier cycles. There were also no significant differences in biochemical pregnancy losses or clinical miscarriage. There were no significant differences noted in low birthweight or high birthweight infants derived from fresh versus frozen donor oocyte after transfer into a gestational carrier.
Conclusions
The analysis of fresh and frozen donor oocytes in gestational carrier cycles provides the opportunity to assess for a possible effect of vitrification on the oocyte by controlling for differences in the uterine environment. We observed no significant differences in live birth, pregnancy loss, low birthweight or high birthweight infants when comparing fresh and frozen donor oocytes in gestational carrier cycles.
Similar content being viewed by others
Data availability
Request to release SART data is required to be processed by the SART research committee (https://www.sart.org/professionals-and-providers/research/).
References
Centers for Disease Control and Prevention. Key statistics from the National Survey of Family Growth – I Listing National Center for Health Statistics [Available from: https://www.cdc.gov/nchs/nsfg/key_statistics/i-keystat.htm#infertility.
Barnhart KT. Assisted reproductive technologies and perinatal morbidity: interrogating the association. Fertil Steril. 2013;99(2):299–302.
Simopoulou M, Sfakianoudis K, Tsioulou P, Rapani A, Anifandis G, Pantou A, et al. Risks in surrogacy considering the embryo: from the preimplantation to the gestational and neonatal period. Biomed Res Int. 2018;2018:6287507.
Center for Disease Control and Prevention. 2020 Assisted reproductive technology fertility clinic and national summary report. US dept of health and human services. 2022.
Chang HY, Hwu WL, Chen CH, Hou CY, Cheng W. Children conceived by assisted reproductive technology prone to low birth weight, preterm birth, and birth defects: a cohort review of more than 50,000 live births during 2011–2017 in Taiwan. Front Pediatr. 2020;8:87.
Homer HA. The role of oocyte quality in explaining “unexplained” unfertility. Semin Reprod Med. 2020;38(1):21–8.
Setti AS, Figueira RC, Braga DP, Colturato SS, Iaconelli A Jr, Borges E Jr. Relationship between oocyte abnormal morphology and intracytoplasmic sperm injection outcomes: a meta-analysis. Eur J Obstet Gynecol Reprod Biol. 2011;159(2):364–70.
Catala MG, Izquierdo D, Rodriguez-Prado M, Hammami S, Paramio MT. Effect of oocyte quality on blastocyst development after in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI) in a sheep model. Fertil Steril. 2012;97(4):1004–8.
Kaser DJ, Reichman DE, Ginsburg ES, Politch JA, Racowsky C. Developmental potential of embryos from intracytoplasmic sperm injection cycles containing fragmented oocytes. Fertil Steril. 2012;97(2):338–43.
Segal TR, Kim K, Mumford SL, Goldfarb JM, Weinerman RS. How much does the uterus matter? Perinatal outcomes are improved when donor oocyte embryos are transferred to gestational carriers compared to intended parent recipients. Fertil Steril. 2018;110(5):888–95.
Practice Committees of the American Society for Reproductive M, Society of Reproductive B, Technologists. Electronic address jao. A review of best practices of rapid-cooling vitrification for oocytes and embryos: a committee opinion. Fertil Steril. 2021;115(2):305–10.
Rudick B, Opper N, Paulson R, Bendikson K, Chung K. The status of oocyte cryopreservation in the United States. Fertil Steril. 2010;94(7):2642–6.
Cobo A, Serra V, Garrido N, Olmo I, Pellicer A, Remohi J. Obstetric and perinatal outcome of babies born from vitrified oocytes. Fertil Steril. 2014;102(4):1006-15 e4.
Shih W, Rushford DD, Bourne H, Garrett C, McBain JC, Healy DL, et al. Factors affecting low birthweight after assisted reproduction technology: difference between transfer of fresh and cryopreserved embryos suggests an adverse effect of oocyte collection. Hum Reprod. 2008;23(7):1644–53.
Wei D, Liu JY, Sun Y, Shi Y, Zhang B, Liu JQ, et al. Frozen versus fresh single blastocyst transfer in ovulatory women: a multicentre, randomised controlled trial. Lancet. 2019;393(10178):1310–8.
Roque M, Haahr T, Geber S, Esteves SC, Humaidan P. Fresh versus elective frozen embryo transfer in IVF/ICSI cycles: a systematic review and meta-analysis of reproductive outcomes. Hum Reprod Update. 2019;25(1):2–14.
Centers for Disease Control and Prevention. 2015 Assisted reproductive technology fertility clinic and national summary report. US dept of health and human services. 2017.
Da Luz CM, Caetano MA, Berteli TS, Vireque AA, Navarro PA. The impact of oocyte vitrification on offspring: a systematic review. Reprod Sci. 2022;29(11):3222–34.
Centers for Disease Control and Prevention. 2019 Assisted reproductive technology fertility clinic and national summary report. US dept of health and human services. 2021.
Practice Committee of the American Society for Reproductive Medicine. Electronic address Aao, Practice Committee of the Society for Assisted Reproductive T. Guidance on the limits to the number of embryos to transfer: a committee opinion. Fertil Steril. 2017;107(4):901–3.
Acknowledgements
The authors thank SART for the dataset, as well as all SART members for providing clinical information to the SART CORS database for use by researchers. Without the efforts of SART members, this research would not have been possible.
Funding
This research was supported in part by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health, Bethesda, Maryland.
Author information
Authors and Affiliations
Contributions
Conceptualization: RW; methodology: CB, APS, SM, RW; formal analysis and investigation: CB APS, ED, SM, RW; writing — original draft preparation: JK, RW; writing — review and editing: JK, CB, APS, ED, SM, RW.
Corresponding author
Ethics declarations
Ethics approval
Not applicable.
Conflict of interest
The authors declare no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Kloos, J., Burks, C., Purdue-Smithe, A. et al. Similar pregnancy outcomes from fresh and frozen donor oocytes transferred to gestational carriers: a SART database analysis isolating the effects of oocyte vitrification. J Assist Reprod Genet 41, 643–648 (2024). https://doi.org/10.1007/s10815-023-03016-2
Received:
Accepted:
Published:
Version of record:
Issue date:
DOI: https://doi.org/10.1007/s10815-023-03016-2