METAPHOR: Metabolic evaluation through phasor-based hyperspectral imaging and organelle recognition for mouse blastocysts and oocytes

Author:

Parra Albert1,Denkova Denitza1ORCID,Burgos-Artizzu Xavier P.12ORCID,Aroca Ester1,Casals Marc1ORCID,Godeau Amélie1,Ares Miguel1ORCID,Ferrer-Vaquer Anna1ORCID,Massafret Ot1,Oliver-Vila Irene3,Mestres Enric4ORCID,Acacio Mònica4,Costa-Borges Nuno4,Rebollo Elena5ORCID,Chiang Hsiao Ju67ORCID,Fraser Scott E.678,Cutrale Francesco67ORCID,Seriola Anna1ORCID,Ojosnegros Samuel1

Affiliation:

1. Institute for Bioengineering of Catalonia, The Barcelona Institute of Science and Technology, Barcelona 08028, Spain

2. Movumtech SL, Madrid 28003, Spain

3. SERABIOTICS SL, Barcelona 08028, Spain

4. Embryotools SL, R&D department, Barcelona 08028, Spain

5. Advanced Fluorescence Microscopy Unit, Molecular Biology Institute of Barcelona (IBMB - CSIC), Barcelona 08028, Spain

6. Translational Imaging Center, University of Southern California, Los Angeles, CA 90089

7. Alfred Mann Department of Biomedical Engineering, University of Southern California, Los Angeles, CA 90089

8. Department of Biological Sciences, Division of Molecular and Computational Biology, University of Southern California, Los Angeles, CA 90089

Abstract

Only 30% of embryos from in vitro fertilized oocytes successfully implant and develop to term, leading to repeated transfer cycles. To reduce time-to-pregnancy and stress for patients, there is a need for a diagnostic tool to better select embryos and oocytes based on their physiology. The current standard employs brightfield imaging, which provides limited physiological information. Here, we introduce METAPHOR: Metabolic Evaluation through Phasor-based Hyperspectral Imaging and Organelle Recognition. This non-invasive, label-free imaging method combines two-photon illumination and AI to deliver the metabolic profile of embryos and oocytes based on intrinsic autofluorescence signals. We used it to classify i) mouse blastocysts cultured under standard conditions or with depletion of selected metabolites (glucose, pyruvate, lactate); and ii) oocytes from young and old mouse females, or in vitro-aged oocytes. The imaging process was safe for blastocysts and oocytes. The METAPHOR classification of control vs. metabolites-depleted embryos reached an area under the ROC curve (AUC) of 93.7%, compared to 51% achieved for human grading using brightfield imaging. The binary classification of young vs. old/in vitro-aged oocytes and their blastulation prediction using METAPHOR reached an AUC of 96.2% and 82.2%, respectively. Finally, organelle recognition and segmentation based on the flavin adenine dinucleotide signal revealed that quantification of mitochondria size and distribution can be used as a biomarker to classify oocytes and embryos. The performance and safety of the method highlight the accuracy of noninvasive metabolic imaging as a complementary approach to evaluate oocytes and embryos based on their physiology.

Publisher

Proceedings of the National Academy of Sciences

Reference56 articles.

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Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. METAPHOR: Metabolic evaluation through phasor-based hyperspectral imaging and organelle recognition for mouse blastocysts and oocytes;Proceedings of the National Academy of Sciences;2024-07-05

2. Automation in the IVF Laboratory;Reference Module in Biomedical Sciences;2024

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