| Literature DB >> 35804050 |
Ronilo Ragodos1, Tong Wang2, Brian J Howe3,4, Carmencita Padilla5, Jacqueline T Hecht6, Fernando A Poletta7, Iêda M Orioli8, Carmen J Buxó9, Azeez Butali10,11, Consuelo Valencia-Ramirez12, Claudia Restrepo Muñeton12, George L Wehby13, Seth M Weinberg14, Mary L Marazita14, Lina M Moreno Uribe11,15.
Abstract
Children with orofacial clefting (OFC) present with a wide range of dental anomalies. Identifying these anomalies is vital to understand their etiology and to discern the complex phenotypic spectrum of OFC. Such anomalies are currently identified using intra-oral exams by dentists, a costly and time-consuming process. We claim that automating the process of anomaly detection using deep neural networks (DNNs) could increase efficiency and provide reliable anomaly detection while potentially increasing the speed of research discovery. This study characterizes the use of` DNNs to identify dental anomalies by training a DNN model using intraoral photographs from the largest international cohort to date of children with nonsyndromic OFC and controls (OFC1). In this project, the intraoral images were submitted to a Convolutional Neural Network model to perform multi-label multi-class classification of 10 dental anomalies. The network predicts whether an individual exhibits any of the 10 anomalies and can do so significantly faster than a human rater can. For all but three anomalies, F1 scores suggest that our model performs competitively at anomaly detection when compared to a dentist with 8 years of clinical experience. In addition, we use saliency maps to provide a post-hoc interpretation for our model's predictions. This enables dentists to examine and verify our model's predictions.Entities:
Mesh:
Year: 2022 PMID: 35804050 PMCID: PMC9270352 DOI: 10.1038/s41598-022-15788-1
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.996
Figure 1Workflow of data analysis. The entire workflow consists of three steps. In step 1, we tune the number of layers to freeze in order to do TL optimally. Our experiments show that when freezing 7 layers, our model achieved the best predictive performance. We then test the model using a fivefold grouped cross-validation. Finally, for each input photo and the corresponding model prediction, we generate a saliency map for each anomaly (regardless of presence in the photo).
Model metrics.
| Anomaly | F1 | Precision | Recall | ROC AUC |
|---|---|---|---|---|
| Mammalons | 0.506 ± 0.077 | 0.482 ± 0.026 | 0.637 ± 0.205 | 0.633 ± 0.122 |
| Impacted | 0.540 ± 0.099 | 0.486 ± 0.163 | 0.774 ± 0.258 | 0.677 ± 0.125 |
| Hypoplasia | 0.561 ± 0.086 | 0.531 ± 0.205 | 0.806 ± 0.272 | 0.708 ± 0.144 |
| Incisal Fissure | 0.531 ± 0.139 | 0.496 ± 0.240 | 0.787 ± 0.212 | 0.651 ± 0.138 |
| Hypocalcification | 0.437 ± 0.059 | 0.397 ± 0.290 | 0.619 ± 0.229 | 0.590 ± 0.089 |
| Displaced | 0.482 ± 0.122 | 0.374 ± 0.115 | 0.729 ± 0.182 | 0.682 ± 0.084 |
| Microdontia | 0.517 ± 0.078 | 0.430 ± 0.140 | 0.670 ± 0.312 | 0.685 ± 0.080 |
| Supernumerary | 0.478 ± 0.101 | 0.534 ± 0.059 | 0.746 ± 0.252 | 0.571 ± 0.123 |
| Rotation | 0.443 ± 0.097 | 0.388 ± 0.154 | 0.868 ± 0.184 | 0.562 ± 0.100 |
| Agenesis | 0.544 ± 0.093 | 0.533 ± 0.231 | 0.728 ± 0.252 | 0.678 ± 0.083 |
Results given are the mean result of all fivefolds with the standard deviation.
LMU pre-calibration metrics.
| Anomaly | F1 | Precision | Recall |
|---|---|---|---|
| Mammalons | 0.857 | 1.000 | 0.750 |
| Impacted | N/A | 0.000 | 0.000 |
| Hypoplasia | 0.667 | 0.500 | 1.000 |
| Incisal Fissure | 0.000 | N/A | 0.000 |
| Hypocalcification | 0.400 | 1.000 | 0.250 |
| Displaced | 0.246 | 0.750 | 0.750 |
| Microdontia | N/A | 0.000 | 0.000 |
| Supernumerary | 0.000 | 0.000 | N/A |
| Rotation | 0.963 | 1.000 | 0.929 |
| Agenesis | 0.000 | 0.000 | 0.000 |
Figure 2Saliency maps. Note: Overlay is the input image overlaid with the gradients. These are representative examples of anomalies depicting what the algorithm saw when making correct predictions of mammalons, hypocalcification, microdontia, and hypoplasia.