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Causal interactions in brain networks predict pain levels in trigeminal neuralgia

Authors :
Yun Liang
Qing Zhao
John K. Neubert
Mingzhou Ding
Source :
Brain Research Bulletin, Vol 211, Iss , Pp 110947- (2024)
Publication Year :
2024
Publisher :
Elsevier, 2024.

Abstract

Trigeminal neuralgia (TN) is a highly debilitating facial pain condition. Magnetic resonance imaging (MRI) is the main method for generating insights into the central mechanisms of TN pain in humans. Studies have found both structural and functional abnormalities in various brain structures in TN patients as compared with healthy controls. Whereas studies have also examined aberrations in brain networks in TN, no studies have to date investigated causal interactions in these brain networks and related these causal interactions to the levels of TN pain. We recorded fMRI data from 39 TN patients who either rested comfortably in the scanner during the resting state session or tracked their pain levels during the pain tracking session. Applying Granger causality to analyze the data and requiring consistent findings across the two scanning sessions, we found 5 causal interactions, including: (1) Thalamus → dACC, (2) Caudate → Inferior temporal gyrus, (3) Precentral gyrus → Inferior temporal gyrus, (4) Supramarginal gyrus → Inferior temporal gyrus, and (5) Bankssts → Inferior temporal gyrus, that were consistently associated with the levels of pain experienced by the patients. Utilizing these 5 causal interactions as predictor variables and the pain score as the predicted variable in a linear multiple regression model, we found that in both pain tracking and resting state sessions, the model was able to explain ∼36 % of the variance in pain levels, and importantly, the model trained on the 5 causal interaction values from one session was able to predict pain levels using the 5 causal interaction values from the other session, thereby cross-validating the models. These results, obtained by applying novel analytical methods to neuroimaging data, provide important insights into the pathophysiology of TN and could inform future studies aimed at developing innovative therapies for treating TN.

Details

Language :
English
ISSN :
18732747
Volume :
211
Issue :
110947-
Database :
Directory of Open Access Journals
Journal :
Brain Research Bulletin
Publication Type :
Academic Journal
Accession number :
edsdoj.4fc3746f5ded44b7b25755cd28154682
Document Type :
article
Full Text :
https://doi.org/10.1016/j.brainresbull.2024.110947