J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, United States.
Department of Orthodontics, University of Florida, Gainesville, FL, United States.
Brain Res Bull. 2024 Jun 1;211:110947. doi: 10.1016/j.brainresbull.2024.110947. Epub 2024 Apr 12.
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.
三叉神经痛(TN)是一种使人高度虚弱的面部疼痛疾病。磁共振成像(MRI)是深入了解人类 TN 疼痛中枢机制的主要方法。研究发现,与健康对照组相比,TN 患者的各种大脑结构存在结构和功能异常。虽然研究也检查了 TN 患者大脑网络中的异常,但迄今为止,尚无研究调查这些大脑网络中的因果关系,并将这些因果关系与 TN 疼痛程度联系起来。我们从 39 名 TN 患者那里记录了 fMRI 数据,这些患者在休息状态会话期间要么在扫描仪中舒适地休息,要么在疼痛跟踪会话期间跟踪他们的疼痛水平。应用格兰杰因果关系来分析数据,并要求在两个扫描会话中都有一致的发现,我们发现了 5 个因果关系,包括:(1)丘脑→dACC,(2)尾状核→颞下回,(3)中央前回→颞下回,(4)缘上回→颞下回,(5)Bankssts→颞下回,这些因果关系与患者经历的疼痛程度一致。利用这 5 个因果关系作为预测变量,将疼痛评分作为预测变量,在线性多元回归模型中,我们发现,在疼痛跟踪和休息状态会话中,该模型都能够解释约 36%的疼痛水平变化,重要的是,在一个会话中训练的基于 5 个因果关系值的模型能够使用另一个会话的 5 个因果关系值来预测疼痛水平,从而对模型进行交叉验证。这些通过应用新的分析方法从神经影像学数据中获得的结果,为 TN 的病理生理学提供了重要的见解,并可能为未来旨在开发治疗 TN 的创新疗法的研究提供信息。