# Recognizing IgA-class endomysial antibody equivalent binding patterns on monkey liver substrate through EfficientNet architectures and deep learning

**Authors:** Mehmet Soylu, Ahmet Selman Bozkir

PMC · DOI: 10.7717/peerj.20191 · PeerJ · 2025-10-15

## TL;DR

This paper shows that deep learning models, particularly EfficientNetV2, can accurately interpret IgA EMA tests for celiac disease, potentially replacing subjective human analysis.

## Contribution

The study introduces a deep learning approach using EfficientNet architectures for automated and accurate classification of IgA EMA-eq test results.

## Key findings

- EfficientNetV2-S achieved 99.37% accuracy in binary classification of IgA EMA-eq test results.
- The model showed 95.28% accuracy in three-class and 86.98% in four-class classification scenarios.
- Medium-sized models outperformed larger ones, and higher input resolution improved performance.

## Abstract

Deep learning offers promising potential for automating the interpretation of immunoglobulin A (IgA) endomysial antibody (EMA) tests, a critical serological test for the diagnosis of celiac disease that currently requires labor-intensive and subjective human interpretation. In this study, we employ and comprehensively evaluate the performance of the EfficientNet and EfficientNetV2 architectures in binary (positive vs negative, where all weak and strong positive signals were grouped as positive), three-class (negative, weak positive, strong positive), and four-class (negative, weak positive, strong positive and gray zone) classification scenarios using immunofluorescence images of IgA EMA equivalent (EMA-eq) tests. Our experiments on 368 clinical samples show high performance, with EfficientNetV2-S achieving an accuracy of 99.37% in binary classification, 95.28% in three-class classification, and 86.98% in the complex four-class scenario that introduces gray zone cases as a distinct interpretive category. Contrary to conventional assumptions, medium-sized deep architectures consistently outperformed their larger counterparts. The superior performance of the EfficientNet-V2 models can be attributed to their architectural innovations and higher input resolution (640 × 640 pixels), which proved critical for capturing subtle immunofluorescence patterns. We also incorporate HiRes-CAM (Class Activation Mapping), a convolutional neural network oriented visual explanation tool, to better understand the decisions of the underlying trained deep learning model in an explainable artificial intelligence (AI) manner. This study demonstrates that deep learning has the potential to achieve expert-level performance in EMA-eq test interpretation, offering a path toward more standardized, efficient and objective celiac disease diagnosis while reducing the burden on specialist medical staff.

## Linked entities

- **Diseases:** celiac disease (MONDO:0005130)

## Full-text entities

- **Genes:** CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}
- **Diseases:** celiac disease (MESH:D002446)
- **Species:** Homo sapiens (human, species) [taxon 9606], Cercopithecidae (monkey, family) [taxon 9527]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12535235/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12535235/full.md

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Source: https://tomesphere.com/paper/PMC12535235