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CLARISA: Connexin-43 Lateralization Automated ROI-Based Image Signal Analyzer
Daniel Gattari1,2, Joseba Sancho-Zamora3, Debora Chan1
1Faculty of Engineering, Austral University, Pilar B1629WWA, Buenos Aires, Argentina.
Insights
A new deep learning framework, CLARISA, enables automated assessment of Connexin-43 (CX43) lateralization in heart tissue. This segmentation-free method simplifies analysis, improving arrhythmia risk evaluation.
Area of Science:
- Cardiovascular pathology
- Biomedical imaging
- Machine learning in histology
Background:
- Connexin-43 (CX43) lateralization in ventricular myocardium is linked to abnormal impulse propagation and arrhythmia susceptibility.
- Quantitative assessment of CX43 lateralization in histological sections is challenging due to complex segmentation requirements.
- Existing methods rely on segmenting individual cardiomyocytes and applying geometric rules, limiting scalability and accuracy.
Purpose of the Study:
- To introduce CLARISA, a novel deep learning framework for segmentation-free, region-of-interest (ROI)-based classification of CX43 lateralization.
- To automate the quantitative assessment of CX43 distribution in cardiac tissue, facilitating arrhythmia risk stratification.
- To develop a method that reduces the annotation burden compared to traditional cell-segmentation approaches.
Main Methods:
- Developed CLARISA, a deep learning framework utilizing a dual-stream EfficientNetV2-S classifier for ROI-based CX43 lateralization classification.
- Generated an expert-annotated dataset from Wistar rat heart cryosections, labeling CX43-positive regions based on distribution patterns.
- Implemented a semi-automated whole-section inference module for generating spatial lateralization probability maps and global estimates.
Main Results:
- CLARISA achieved high performance on a held-out test set with ROC-AUC of 0.904 and PR-AUC of 0.808.
- Whole-section analysis generated spatial maps reflecting heterogeneous CX43 organization and provided global estimates closely aligned with expert annotations.
- The ROI-based approach demonstrated a non-equivalent but related readout to cell-segmentation methods, with reduced annotation complexity.
Conclusions:
- CLARISA represents a proof-of-principle for scalable, segmentation-free assessment of CX43 lateralization in cardiac tissue.
- The framework simplifies quantitative analysis of CX43 distribution, offering potential for improved arrhythmia risk assessment.
- Further validation on diverse datasets is needed to confirm robustness, portability, and translational applicability.
Abstract:
Connexin-43 (CX43) lateralization in ventricular myocardium has been associated with abnormal impulse propagation and increased arrhythmia susceptibility. Its quantitative assessment in histological sections remains challenging because previous methods require segmentation of individual cardiomyocytes and rely on geometric rules applied to segmented cell profiles. Here, we present CLARISA, a segmentation-free, ROI-based deep learning framework that classifies CX43-positive regions as terminal or lateralized directly from fluorescence images. An expert-annotated dataset was generated from left-ventricular cryosections of Wistar rat hearts, in which CX43-positive regions were labeled according to their distribution pattern. A dual-stream EfficientNetV2-S classifier was trained to capture both local and contextual ROI morphology. We also developed a semi-automated whole-section inference module to generate spatial lateralization probability maps and global percent lateralization estimates. On the held-out test set, CLARISA achieved a ROC-AUC of 0.904 (95% bootstrap CI: 0.828-0.960) and a PR-AUC of 0.808 (95% bootstrap CI: 0.682-0.913), supporting the feasibility of automated ROI classification for CX43 lateralization assessment. When deployed on whole tissue sections, including an independently analyzed section not used during model development, CLARISA generated spatial maps that captured heterogeneous CX43 organization and produced a global percent lateralization estimate closely aligned with expert annotation, differing by only 1.30 percentage points over the same detected CX43-positive area. Comparison with a previously published segmentation-based method further indicated that ROI-based and cell-segmentation-based approaches provide related but non-equivalent readouts of CX43 lateralization. The ROI-based design additionally reduces annotation burden-requiring classification of discrete CX43-positive signal rather than complex cardiomyocyte delineation-and ensures that all detected CX43-positive signal contributes to the lateralization estimate regardless of cell boundaries. These results establish CLARISA as a proof-of-principle framework for scalable, segmentation-free CX43 lateralization assessment in cardiac tissue. Further validation across larger, independent, and more heterogeneous datasets will be required to assess robustness, portability across imaging conditions, and translational applicability. The complete codebase, pretrained model, image data, and expert annotation tool are publicly available.
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