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Brain aging among individuals with trigeminal neuralgia
Yenisel Cruz-Almeida1,2,3, Pedro A Valdes-Hernandez1,4, Yun Liang5
1Pain Research & Intervention Center of Excellence, University of Florida, Gainesville, FL, United States.
Neurobiology of Pain (Cambridge, Mass.)
|November 10, 2025
Summary
Classical trigeminal neuralgia (TN) is linked to accelerated brain aging, unlike secondary TN. Brain aging differences correlate with pain catastrophizing and anxiety in classical TN patients.
Area of Science:
- Neuroscience
- Radiology
- Psychology
Background:
- Trigeminal neuralgia (TN) is a neuropathic pain condition with poorly understood mechanisms.
- Brain changes, including accelerated aging, are increasingly implicated in TN.
- Brain aging biomarkers offer potential insights into TN pathophysiology.
Purpose of the Study:
- To assess predicted brain age difference (brain-PAD) in classical TN and secondary/idiopathic TN subtypes.
- To compare brain-PAD between TN subtypes and pain-free controls.
- To investigate associations between brain-PAD and clinical/psychological factors in TN.
Main Methods:
- Cross-sectional study comparing classical TN (n=34), secondary/idiopathic TN (n=17), and controls (n=54).
- T1 brain MRI scans were acquired for all participants.
- Brain-PAD was calculated using validated biomarkers; clinical and psychological data were collected.
Main Results:
- Classical TN showed significantly greater brain-PAD (3.87 years) compared to controls (p=0.01).
- No significant brain-PAD differences were found between secondary/idiopathic TN and controls.
- Brain-PAD positively correlated with pain catastrophizing and pain-related anxiety in classical TN (p<0.05).
Conclusions:
- Accelerated brain aging is associated with classical TN, but not secondary/idiopathic TN.
- Brain aging in classical TN is linked to psychological factors, not disease duration or intensity.
- Brain aging biomarkers derived from clinical MRI scans may aid TN research and understanding.

