GENERAL COMMENTARY article
Commentary: A Novel Predictive Model to Estimate the Number of Mature Oocytes Required for Obtaining at Least One Euploid Blastocyst for Transfer in Couples Undergoing in vitro Fertilization/Intracytoplasmic Sperm Injection: The ART Calculator
- Fertility Center Hamburg, Hamburg, Germany
A Commentary on
A Novel Predictive Model to Estimate the Number of Mature Oocytes Required for Obtaining at Least One Euploid Blastocyst for Transfer in Couples Undergoing in vitro Fertilization/Intracytoplasmic Sperm Injection: The ART Calculator
by Esteves, S. C., Carvalho, J. F., Bento, F. C., and Santos, J. (2019). Front. Endocrinol. 10:99. doi: 10.3389/fendo.2019.00099
As elaborated in the excellent paper by Haahr et al. (1) the POSEIDON group 3 (POR patients below the age of 35 years) represent a much easier to treat entity than their older counterparts. In general their chance of producing aneuploid embryos is considerably lower than in women of older age. According to Franasiak et al. (2) the aneuploidy rate identified on the basis of 221 trophectoderm biopsies is 31.3% at the age of 34 years, increasing steadily to over 80% at age 43 and onwards. Therefore, the likelihood of transferring a euploid embryo is high in POSEIDON group 3 patients, even in cases where only two embryos develop from fertilized oocytes. This nevertheless underlines the importance of maximizing the number of good quality mature oocytes by choosing the best individual stimulation approach possible (3). Because there may be considerable high individual variation in the rate of oocyte aneuploidy and resulting embryos even in young patients as has been shown by Minasi et al. (4) it may be worth to clarify the situation of chromosomal problems in the oocytes at an early stage of treatment—i.e., during the first treatment cycle. In countries where embryo biopsy is legally not permitted (like Germany) this can be achieved by performing biopsies on the two polar bodies from normally fertilized oocytes. This will cover only the maternal contribution to chromosomal mal-distribution which nevertheless represents the vast majority of these problems. The high concordance rate of polar body results and the chromosomal constitution of the corresponding oocytes has been well-documented (5). If the results for an individual patient show normal-for-age aneuploidy rates subsequent therapies can focus on optimization of oocyte yield while PGT-A may be added as an adjunct technology for cases identified to have higher rates to spare the patient unnecessary transfers or spontaneous abortions. Application of polar body genetic analysis in patients of POSEIDON groups 3 and 4 with high aneuploidy rates has the additional advantage to allow for fresh transfer of identified euploid embryos in the same cycle thus avoiding the risk of losing precious material during freezing and thawing procedures, and also avoiding the need for prolonged culture to the blastocyst. This may facilitate even POR patients of younger age to shorten the time-to-pregnancy or rather time-to-Live-Birth.
The paper by Haahr et al. (1) is presently the best available guidance for the clinician faced with patients presenting with reduced ovarian reserve to individually tailor the approach to therapy to offer the maximum chance for pregnancy and birth. The additional detailed presentation of information on adjuvant therapies opens the path for further clinical research about their relevance in improving the perspective for all POR patients. Especially for women meeting the POSEIDON group 3 criteria this is the perfect assistance to enable the achievement of live birth rates above 20% by taking the best possible path from the very beginning of the treatment.
VB preparation of manuscript. RF revision and completion. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
2. Franasiak JM, Forman EJ, Hong KH, Werner MD, Upham KM, Treff NR, et al. The nature of aneuploidy with increasing age of the female partner: a review of 15,169 consecutive trophectoderm biopsies evaluated with comprehensive chromosomal screening. Fertil Steril. (2014) 101:656–63.e1. doi: 10.1016/j.fertnstert.2013.11.004
3. Drakopoulos P, Santos-Ribeiro S, Bosch E, Garcia-Velaso J, Blockeel C, Romito A, et al. The effect of dose adjustments in a subsequent cycle of women with suboptimal response following conventional ovarian stimulation. Front Endocrinol. (2018) 9:361. doi: 10.3389/fendo.2018.00361
4. Minasi MG, Colasante A, Ricchio T, Riberti A, Caciani V, Scarselli F, et al. Correlation between aneuploidy, standard morphology evaluation and morphokinetic development in 1730 biopsied blastocysts: a consecutive case series study. Hum Reprod. (2016) 31:2245–54. doi: 10.1093/humrep/dew183
Keywords: mathematical model, age effect, mature oocytes, blastocyst transfer, euploidy
Citation: Fischer R and Baukloh V (2020) Commentary: A Novel Predictive Model to Estimate the Number of Mature Oocytes Required for Obtaining at Least One Euploid Blastocyst for Transfer in Couples Undergoing in vitro Fertilization/Intracytoplasmic Sperm Injection: The ART Calculator. Front. Endocrinol. 11:618. doi: 10.3389/fendo.2020.00618
Received: 12 December 2019; Accepted: 29 July 2020;
Published: 02 September 2020.
Edited by:Leif Johan Bungum, Trianglen Fertility Clinic, Denmark
Reviewed by:Sven Olaf Skouby, University of Copenhagen, Denmark
Copyright © 2020 Fischer and Baukloh. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Robert Fischer, firstname.lastname@example.org