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Peripheral/central neural microstructural alterations in persistent idiopathic dentoalveolar pain: a case-comparative
Motoko Watanabe1, Keigo Shimoji2, Junichiro Sakamoto3
1Department of Psychosomatic Dentistry, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, Japan.
Frontiers in Neurology
|August 7, 2026
Summary
Persistent idiopathic dentoalveolar pain (PIDAP) may involve distinct peripheral or central mechanisms, influenced by neurovascular compression (NVC). Research shows NVC impacts the trigeminal nerve, while its absence links to white matter changes and heightened pain.
Area of Science:
- Neurology
- Pain Medicine
- Neuroimaging
Background:
- Persistent idiopathic dentoalveolar pain (PIDAP) mechanisms are unclear, with theories suggesting peripheral or central nervous system involvement.
- Understanding these mechanisms is crucial for effective PIDAP diagnosis and treatment.
Purpose of the Study:
- To investigate differences in clinical characteristics and white matter integrity in PIDAP patients.
- To compare neural integrity at the peripheral trigeminal nerve and central white matter based on the presence or absence of neurovascular compression (NVC).
Main Methods:
- Retrospective case-comparative study of PIDAP patients undergoing diffusion tensor imaging (DTI).
- Fractional anisotropy (FA) assessed trigeminal nerve integrity at the root entry zone (REZ) and central white matter integrity.
- Clinical characteristics including pain intensity, pain catastrophizing, and Somatic Symptoms Scale-8 (SSS-8) were analyzed.
Main Results:
- Patients without NVC reported significantly higher pain intensity compared to those with NVC.
- NVC presence correlated with reduced FA in the trigeminal nerve, while absence showed a trend toward reduced FA in white matter.
- Asymmetric FA patterns in pain-related brain regions were observed in all PIDAP patients, irrespective of NVC.
- Correlations between FA, clinical scores, and NVC status varied, suggesting distinct pathophysiological pathways.
Conclusions:
- PIDAP may comprise subgroups with predominantly peripheral (with NVC) or central (without NVC) mechanisms.
- PIDAP with NVC is linked to peripheral trigeminal nerve changes and central alterations related to somatic burden.
- PIDAP without NVC appears associated with central white matter alterations in pain-related regions, correlating with pain severity.
- Asymmetric FA patterns in specific brain regions may represent a common feature of PIDAP.

