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Synthetic data augmentation for CT-based emphysema subtype classification: A comparative evaluation of generative and classical approaches.

Created on 21 Aug 2026

Authors

Nicholas Dietrich, David McShannon

Published in

PloS one. Volume 21. Issue 8. Pages e0355850. Epub Aug 20, 2026.

Abstract

Data scarcity is a persistent challenge in medical image analysis. Synthetic data generation using deep generative models has been proposed as a potential approach to address this limitation, yet its performance in small-data settings remains poorly characterized. This study compared three class-conditional generative approaches, a conditional variational autoencoder (cVAE), a conditional shallow-decoder VAE variant (cSD-VAE), and a conditional Wasserstein GAN with gradient penalty (cWGAN-GP), against classical geometric augmentation for emphysema subtype classification on 168 CT patches (three classes: normal tissue, centrilobular emphysema, and paraseptal emphysema). Each method was evaluated at three synthetic-to-real ratios (0.5x, 1.0x, 2.0x) using patient-level 70/30 splits across 10 random seeds, with an ImageNet-pretrained ResNet18 as the downstream classifier. No individual augmentation strategy produced a statistically significant improvement in balanced accuracy over the unaugmented baseline (0.522 ± 0.067). The conditional WGAN-GP at 1.0x achieved the highest individual balanced accuracy (0.548 ± 0.068, Cohen's d = 0.47 versus baseline), but did not reach statistical significance (p = 0.084). A pre-specified ensemble combining all four augmentation methods at the 1.0x multiplier did not significantly improve balanced accuracy over baseline (0.541 ± 0.088 versus 0.522 ± 0.067; Cohen's d = 0.32, Wilcoxon p = 0.275). Neither pixel-space nor feature-space distributional fidelity was associated with downstream classification performance. Overall, no benefit was detected from class-conditional generative augmentation in this small-data, texture-driven setting. Future work should focus on improving generative modeling under small-data conditions, including task-aware objectives and pathology-constrained synthesis.

PMID:
42623403
Bibliographic data and abstract were imported from PubMed on 21 Aug 2026.

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