Embryo Quality Evaluation via Multi-Stage Movement Feature Analysis

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Solution Overview

Problem

Existing embryo quality evaluation techniques for IVF, such as PTL 1, are insufficient in accuracy as they rely solely on changes in embryo shape at the 1-cell stage, failing to distinguish high-quality embryos effectively, which limits the prediction of embryonic development potential and pregnancy success.

Innovation Solution

An information processing system that captures and analyzes the movement of embryos across multiple cell stages using image analysis, specifying motion vectors and calculating movement feature values to evaluate embryo quality accurately.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Device complexity

If only changes in embryo shape at the 1-cell stage are used for evaluation, then the evaluation process is simple, but the prediction accuracy of embryo quality is insufficient

Engineering Contradiction:
Improveevaluation process complexityVSAvoidembryo quality prediction accuracy
Core Design Contradiction:
Device complexityVSMeasurement precision

Solution Approach 1:

The patent transitions from evaluating only spatial changes (shape) at a single time point to evaluating temporal changes (movement over time) across multiple cell stages. This adds the time dimension to the evaluation, enabling measurement of intracytoplasmic movement patterns that correlate with embryo quality without significantly increasing system complexity

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

Solution Approach 2:

The patent changes the evaluation parameter from static shape characteristics to dynamic movement characteristics. By measuring intracytoplasmic movement through image analysis of embryos at multiple cell stages (2-cell, 4-cell, 8-cell), the system captures temporal dynamics that provide more accurate quality prediction while maintaining a relatively simple evaluation framework

Inventive Principle:
Principle #35Parameter changes

2Measurement precision

If multiple cell stages are analyzed to improve prediction accuracy, then the measurement precision increases, but the complexity of the evaluation system increases

Engineering Contradiction:
Improveembryo quality evaluation accuracyVSAvoidevaluation system complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent segments the evaluation process into distinct cell stage intervals (1-cell to 2-cell, 2-cell to 4-cell, 4-cell to 8-cell), analyzing movement characteristics at each transition. This segmentation allows comprehensive multi-stage evaluation while organizing the complexity into manageable, standardized analysis units that can be processed systematically

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent uses image analysis to create digital representations of embryo movement patterns across multiple cell stages. By capturing and analyzing images at standardized intervals, the system replicates the evaluation process across different time points without requiring physical manipulation or complex experimental setups, thereby increasing precision while controlling system complexity

Inventive Principle:
Principle #26Copying

Data Source

PatentEP3485458B1Information processing device, information processing method, and information processing system
Publication Date: 2021.08.25 SONY GROUP CORP
  • EP3485458B1 patent drawingFigure 1
  • EP3485458B1 patent drawingFigure 2
  • EP3485458B1 patent drawingFigure 3

AI summary

There is provided an information processing device including: an analysis unit that specifies a movement in a region-of-interest relating to an embryo on a plurality of images using the plurality of images including the embryo captured in a time series manner during periods corresponding to a plurality of cell stages; a feature value calculation unit that calculates a movement feature value relating to an inside of the embryo on the basis of the specified movement; and a presentation control unit that controls a presentation of the movement feature values acquired during periods corresponding to at least two cell stages among the plurality of cell stages in order to evaluate a quality of the embryo.