# Decoding adolescent TMJ osteoarthritis with multimodal machine learning

**Authors:** Yeon-Hee Lee, Do-Hoon Kim, Akhilanand Chaurasia, Tae-Seok Kim, Fernando P.S. Guastaldi, Yung-Kyun Noh

PMC · DOI: 10.22514/jofph.2026.021 · 2026-03-12

## TL;DR

This study uses machine learning to improve the diagnosis of adolescent TMJ osteoarthritis by combining clinical and imaging data.

## Contribution

The study introduces a multimodal machine learning approach to enhance diagnostic accuracy for adolescent TMJ-OA.

## Key findings

- Imaging-only models showed high specificity but low sensitivity for TMJ-OA diagnosis.
- Combining clinical and imaging data improved sensitivity and model performance.
- Panoramic radiography was the strongest predictor in the decision tree models.

## Abstract

Background: Early and accurate diagnosis of adolescent 
temporomandibular joint (TMJ) osteoarthritis (OA) is critical, as degenerative 
changes during growth can cause lifelong pain and deformity. This study aimed to 
identify key clinical and imaging predictors of adolescent TMJ-OA and to evaluate 
multimodal machine learning models. Methods: The diagnostic utility was 
evaluated in 79 adolescents (10–18 years) with TMJ pain using panoramic 
radiography (PR) and MRI. TMJ-OA was diagnosed based on the Diagnostic Criteria 
for Temporomandibular Disorders (DC/TMD). Three decision tree models were 
developed: Model 1 (clinical-only), Model 2 (imaging-only), and Model 3 (combined 
clinical and imaging). Logistic regression was used for the comparisons. 
Results: To ensure a robust evaluation with a small sample size (n = 
79), the models were assessed using nested 5-fold cross-validation. Model 2 
(imaging only) had the highest specificity (0.7714 ± 0.2321), accuracy 
(0.5942 ± 0.0966), and AUROC (0.719 ± 0.101), but a low sensitivity 
(0.4472 ± 0.2065). PR evidence of TMJ-OA (feature importance = 0.70; OR = 
3.93) was the strongest predictor and root node in the decision tree. Model 3 
(combined clinical and imaging data) showed improved sensitivity (0.6056 ± 
0.1829), identifying PR_TMJ_OA, MRI_TMJ_ADD (anterior disc displacement), 
Visual Analog Scale (VAS) score, and age as key nodes (AUROC = 0.6573 ± 
0.0338; OR = 2.85 for PR_TMJ_OA). Model 1 (clinical-only) had limited 
predictive performance (AUROC = 0.4859 ± 0.0894), with symptom duration 
(importance = 0.64; OR = 1.40), VAS score, and joint locking (importance = 0.20) 
contributing modestly. A model using PR_TMJ_OA alone achieved perfect 
specificity (0.9714 ± 0.0571) but low sensitivity (0.3806 ± 0.1458). 
Conclusions: Although PR is a meaningful screening tool for adolescent 
TMJ-OA, it remains insufficient as a standalone diagnostic modality. Multimodal 
integration of clinical and MRI findings improves diagnostic accuracy and 
provides interpretable, clinically aligned decision-support tools for TMJ-OA.

## Linked entities

- **Diseases:** osteoarthritis (MONDO:0005178)

## Full-text entities

- **Genes:** PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}
- **Diseases:** synovitis (MESH:D013585), DC (MESH:D054221), joint  degeneration (MESH:D009410), joint locking (MESH:D000080422), congenital craniofacial anomalies (MESH:D019465), degenerative  disease (MESH:D019636), inflammation (MESH:D007249), OA (MESH:D010003), rheumatoid arthritis (MESH:D001172), genetic syndromes (MESH:D030342), erosion (MESH:D014077), cleft lip/palate (MESH:D002971), disc (MESH:D055959), skeletal discrepancies (MESH:C564967), sclerosis (MESH:D012598), ADD (MESH:D007405), Pain (MESH:D010146), muscle  stiffness (MESH:D019042), chronic pain (MESH:D059350), subchondral cysts (MESH:D001845), osteophyte (MESH:D054850), cognitive disorders (MESH:D003072), DC/TMD (MESH:D013705), effusion (MESH:D000080324), juvenile idiopathic arthritis (MESH:D001171), joint damage (MESH:D007592), TMJ  osteoarthritis (MESH:D013706), condylar degeneration (MESH:C538270), Bruxism (MESH:D002012), RDC (MESH:C535684), craniosynostosis (MESH:D003398), occlusal (MESH:D001157), deformities (MESH:D009140), jaw locking (MESH:D014313), TMD (MESH:D049310), fracture injury (MESH:D008337), impairment (MESH:D060825), orofacial pain (MESH:D005157)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13036619/full.md

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Source: https://tomesphere.com/paper/PMC13036619