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Background <p>Artificial intelligence can standardize periapical assessment, but few studies map pixel-level segmentation to clinically interpretable Periapical Index (PAI) categories under a unified protocol.</p> Methods <p>We retrospectively assembled 900 anonymized periapical radiographs with expert masks and patient-level splits (train/val/test: 594/145/161). Four architectures (U-Net, ResUNet34, DeepLabV3, HRNet) were trained with identical preprocessing, augmentation, and binary cross-entropy (BCE) + Dice loss. On the independent test set, segmentation and image-level detection (sensitivity, specificity, precision, F1, AUC) were computed at a prespecified operating point. An area-based PAI score (aPAI) was derived from lesion-to-image area ratios using prespecified thresholds, providing a quantitative, size-based proxy for conventional PAI categories that does not incorporate qualitative radiographic features such as border definition or trabecular changes.</p> Results <p>DeepLabV3 achieved the most balanced detection (accuracy 90.1%, sensitivity 92.8%, F1 91.8%), while HRNet yielded the highest specificity (87.5%) and precision (91.4%). Friedman/Wilcoxon analyses showed significant overall between-model differences. After Bonferroni correction (adjusted α = 0.0083), only the DeepLabV3 versus U-Net comparison remained statistically significant for both binary lesion detection and aPAI classification (both <i>p</i> = 0.0012); no other pairwise differences reached the corrected threshold. aPAI classification accuracy ranged from 72.7% (U-Net) to 84.5% (DeepLabV3).</p> Conclusions <p>Segmentation-based, area-derived PAI scoring is feasible and consistent across architectures. DeepLabV3 is preferable for screening workflows requiring high sensitivity, whereas HRNet minimizes false positives for confirmatory use. The unified pipeline provides an interpretable bridge from pixel probabilities to standard PAI categories.</p>

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Automated periapical lesion segmentation and area-based PAI indexing: a comparative deep learning study on periapical radiographs

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年5月18日

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  • Damla Erkal,
  • Yunus Emre Çakmak,
  • Kürşat Er,
  • Alper Kuştarcı

摘要

Background

Artificial intelligence can standardize periapical assessment, but few studies map pixel-level segmentation to clinically interpretable Periapical Index (PAI) categories under a unified protocol.

Methods

We retrospectively assembled 900 anonymized periapical radiographs with expert masks and patient-level splits (train/val/test: 594/145/161). Four architectures (U-Net, ResUNet34, DeepLabV3, HRNet) were trained with identical preprocessing, augmentation, and binary cross-entropy (BCE) + Dice loss. On the independent test set, segmentation and image-level detection (sensitivity, specificity, precision, F1, AUC) were computed at a prespecified operating point. An area-based PAI score (aPAI) was derived from lesion-to-image area ratios using prespecified thresholds, providing a quantitative, size-based proxy for conventional PAI categories that does not incorporate qualitative radiographic features such as border definition or trabecular changes.

Results

DeepLabV3 achieved the most balanced detection (accuracy 90.1%, sensitivity 92.8%, F1 91.8%), while HRNet yielded the highest specificity (87.5%) and precision (91.4%). Friedman/Wilcoxon analyses showed significant overall between-model differences. After Bonferroni correction (adjusted α = 0.0083), only the DeepLabV3 versus U-Net comparison remained statistically significant for both binary lesion detection and aPAI classification (both p = 0.0012); no other pairwise differences reached the corrected threshold. aPAI classification accuracy ranged from 72.7% (U-Net) to 84.5% (DeepLabV3).

Conclusions

Segmentation-based, area-derived PAI scoring is feasible and consistent across architectures. DeepLabV3 is preferable for screening workflows requiring high sensitivity, whereas HRNet minimizes false positives for confirmatory use. The unified pipeline provides an interpretable bridge from pixel probabilities to standard PAI categories.