The impact of endometriosis on embryo morphokinetics: embryos from endometriosis patients exhibit delayed cell cycle milestones and decreased blastulation rates

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Embryos from endometriosis patients showed delayed cell cycle progression and reduced blastulation rates compared to controls, yet IVF outcomes were similar.

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This retrospective study compared embryo morphokinetics between 1,078 embryos from women with endometriosis and 2,393 embryos from controls across 434 IVF oocyte retrievals at a single academic center, using time-lapse incubator monitoring up to 6 days and retrospectively reviewing prospectively collected morphokinetic data and cycle outcomes. Embryos from the endometriosis group showed delayed early cell-cycle milestones (slower to reach the 2–8 cell stages), delayed compaction, and delayed late events including morulation and blastulation, and were less likely to progress to morula, blastocyst, and expanded blastocyst stages; fewer embryos also fell within reported optimal kinetic ranges for several timepoints. Despite these developmental differences, clinical pregnancy and live birth rates did not differ significantly between groups. The paper relates to endometriosis because it directly tests whether endometriosis-associated embryo cohorts display altered morphokinetics and lower progression to key developmental stages.

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Abstract

Purpose To compare morphokinetic parameters in embryos obtained from women with and without endometriosis.

Methods

We evaluated a total of 3471 embryos resulting from 434 oocyte retrievals performed at a single academic center. One thousand seventy-eight embryos were obtained from women affected by endometriosis and 2393 came from unaffected controls. All embryos were cultured in a time-lapse incubator chamber for up to 6 days. IVF cycle outcomes and morphokinetic parameters collected prospectively were retrospectively reviewed.

Results

Morphokinetic data suggest that embryo development is impaired in embryos obtained from women with endometriosis (EE). EE were slower to achieve the 2–8 cell stages compared to control embryos (CE) (p < 0.001); additionally, time to compaction was delayed compared to CE (p = 0.015). The timing of late developmental events, including morulation and blastulation was also delayed in the endometriosis cohort (p < 0.001). In addition to demonstrating delayed cell cycle milestones, EE were less likely than controls to progress to morula, blastocyst, and expanded blastocyst stages (p < 0.001). Furthermore, a smaller proportion of embryos in the endometriosis group fell into optimal kinetic ranges for cc2 (p = 0.003), t5 (p = 0.019), tSB (p < 0.001), and tEB (p = 0.007). There were no significant differences in clinical pregnancy or live birth rates between groups.

Conclusion

Embryos from endometriosis patients demonstrate impairments in both early and late developmental events, and progress to the morula, blastocyst, and expanded blastocyst stages at lower rates than control embryos. Despite these differences, IVF outcomes are similar for patients with and without endometriosis. Similar content being viewed by others

References

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Acknowledgements

We would like to acknowledge Lin Mei for her excellent assistance with extracting patient medical records from the electronic medical record system. Author information Authors and Affiliations Corresponding author Ethics declarations Ethics approval This study was approved by the Cleveland Clinic Institutional Review Board (IRB # 19–997). 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. Supplementary Information Below is the link to the electronic supplementary material. Rights and permissions About this article Cite this article Llarena, N.C., Hur, C.E., Yao, M. et al. The impact of endometriosis on embryo morphokinetics: embryos from endometriosis patients exhibit delayed cell cycle milestones and decreased blastulation rates. J Assist Reprod Genet 39, 619–628 (2022). https://doi.org/10.1007/s10815-022-02406-2 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s10815-022-02406-2

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endometriosis

MeSH descriptors

Endometriosis Endometriosis Blastocyst Cell Cycle Embryo Culture Techniques Embryonic Development Embryonic Development Female Humans Pregnancy Retrospective Studies Time-Lapse Imaging

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