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Delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation

PURPOSE: Our objective was to design an automated deep learning model that extracts the morphokinetic events of embryos that were recorded by time-lapse incubators. Using automated annotation, we set out to characterize the temporal heterogeneity of preimplantation development across a large number...

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Autores principales: Zabari, Nir, Kan-Tor, Yoav, Or, Yuval, Shoham, Zeev, Shufaro, Yoel, Richter, Dganit, Har-Vardi, Iris, Ben-Meir, Assaf, Srebnik, Naama, Buxboim, Amnon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310622/
https://www.ncbi.nlm.nih.gov/pubmed/37300648
http://dx.doi.org/10.1007/s10815-023-02806-y
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author Zabari, Nir
Kan-Tor, Yoav
Or, Yuval
Shoham, Zeev
Shufaro, Yoel
Richter, Dganit
Har-Vardi, Iris
Ben-Meir, Assaf
Srebnik, Naama
Buxboim, Amnon
author_facet Zabari, Nir
Kan-Tor, Yoav
Or, Yuval
Shoham, Zeev
Shufaro, Yoel
Richter, Dganit
Har-Vardi, Iris
Ben-Meir, Assaf
Srebnik, Naama
Buxboim, Amnon
author_sort Zabari, Nir
collection PubMed
description PURPOSE: Our objective was to design an automated deep learning model that extracts the morphokinetic events of embryos that were recorded by time-lapse incubators. Using automated annotation, we set out to characterize the temporal heterogeneity of preimplantation development across a large number of embryos. METHODS: To perform a retrospective study, we used a dataset of video files of 67,707 embryos from four IVF clinics. A convolutional neural network (CNN) model was trained to assess the developmental states that appear in single frames from 20,253 manually-annotated embryos. Probability-weighted superposition of multiple predicted states was permitted, thus accounting for visual uncertainties. Superimposed embryo states were collapsed onto discrete series of morphokinetic events via monotonic regression of whole-embryo profiles. Unsupervised K-means clustering was applied to define subpopulations of embryos of distinctive morphokinetic profiles. RESULTS: We perform automated assessment of single-frame embryo states with 97% accuracy and demonstrate whole-embryo morphokinetic annotation with R-square 0.994. High quality embryos that had been valid candidates for transfer were clustered into nine subpopulations, as characterized by distinctive developmental dynamics. Retrospective comparative analysis of transfer versus implantation rates reveals differences between embryo clusters as marked by poor synchronization of the third mitotic cell-cleavage cycle. CONCLUSIONS: By demonstrating fully automated, accurate, and standardized morphokinetic annotation of time-lapse embryo recordings from IVF clinics, we provide practical means to overcome current limitations that hinder the implementation of morphokinetic decision-support tools within clinical IVF settings due to inter-observer and intra-observer manual annotation variations and workload constrains. Furthermore, our work provides a platform to address embryo heterogeneity using dimensionality-reduced morphokinetic descriptions of preimplantation development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10815-023-02806-y.
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spelling pubmed-103106222023-07-01 Delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation Zabari, Nir Kan-Tor, Yoav Or, Yuval Shoham, Zeev Shufaro, Yoel Richter, Dganit Har-Vardi, Iris Ben-Meir, Assaf Srebnik, Naama Buxboim, Amnon J Assist Reprod Genet Assisted Reproduction Technologies PURPOSE: Our objective was to design an automated deep learning model that extracts the morphokinetic events of embryos that were recorded by time-lapse incubators. Using automated annotation, we set out to characterize the temporal heterogeneity of preimplantation development across a large number of embryos. METHODS: To perform a retrospective study, we used a dataset of video files of 67,707 embryos from four IVF clinics. A convolutional neural network (CNN) model was trained to assess the developmental states that appear in single frames from 20,253 manually-annotated embryos. Probability-weighted superposition of multiple predicted states was permitted, thus accounting for visual uncertainties. Superimposed embryo states were collapsed onto discrete series of morphokinetic events via monotonic regression of whole-embryo profiles. Unsupervised K-means clustering was applied to define subpopulations of embryos of distinctive morphokinetic profiles. RESULTS: We perform automated assessment of single-frame embryo states with 97% accuracy and demonstrate whole-embryo morphokinetic annotation with R-square 0.994. High quality embryos that had been valid candidates for transfer were clustered into nine subpopulations, as characterized by distinctive developmental dynamics. Retrospective comparative analysis of transfer versus implantation rates reveals differences between embryo clusters as marked by poor synchronization of the third mitotic cell-cleavage cycle. CONCLUSIONS: By demonstrating fully automated, accurate, and standardized morphokinetic annotation of time-lapse embryo recordings from IVF clinics, we provide practical means to overcome current limitations that hinder the implementation of morphokinetic decision-support tools within clinical IVF settings due to inter-observer and intra-observer manual annotation variations and workload constrains. Furthermore, our work provides a platform to address embryo heterogeneity using dimensionality-reduced morphokinetic descriptions of preimplantation development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10815-023-02806-y. Springer US 2023-06-10 2023-06 /pmc/articles/PMC10310622/ /pubmed/37300648 http://dx.doi.org/10.1007/s10815-023-02806-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Assisted Reproduction Technologies
Zabari, Nir
Kan-Tor, Yoav
Or, Yuval
Shoham, Zeev
Shufaro, Yoel
Richter, Dganit
Har-Vardi, Iris
Ben-Meir, Assaf
Srebnik, Naama
Buxboim, Amnon
Delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation
title Delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation
title_full Delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation
title_fullStr Delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation
title_full_unstemmed Delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation
title_short Delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation
title_sort delineating the heterogeneity of embryo preimplantation development using automated and accurate morphokinetic annotation
topic Assisted Reproduction Technologies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310622/
https://www.ncbi.nlm.nih.gov/pubmed/37300648
http://dx.doi.org/10.1007/s10815-023-02806-y
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