Kincses Balint, Forkmann Katarina, Schlitt Frederik, Jan Pawlik Robert, Schmidt Katharina, Timmann Dagmar, Elsenbruch Sigrid, Wiech Katja, Bingel Ulrike, Spisak Tamas
Department of Neurology, Center for Translational Neuro- and Behavioral Sciences, University Medicine Essen, Essen, Germany.
Institute for Diagnostic and Interventional Radiology and Neuroradiology, University Medicine Essen, Essen, Germany.
Commun Biol. 2024 Jul 17;7(1):875. doi: 10.1038/s42003-024-06574-y.
Pain can be conceptualized as a precision signal for reinforcement learning in the brain and alterations in these processes are a hallmark of chronic pain conditions. Investigating individual differences in pain-related learning therefore holds important clinical and translational relevance. Here, we developed and externally validated a novel resting-state brain connectivity-based predictive model of pain-related learning. The pre-registered external validation indicates that the proposed model explains 8-12% of the inter-individual variance in pain-related learning. Model predictions are driven by connections of the amygdala, posterior insula, sensorimotor, frontoparietal, and cerebellar regions, outlining a network commonly described in aversive learning and pain. We propose the resulting model as a robust and highly accessible biomarker candidate for clinical and translational pain research, with promising implications for personalized treatment approaches and with a high potential to advance our understanding of the neural mechanisms of pain-related learning.
疼痛可被概念化为大脑中强化学习的精确信号,而这些过程的改变是慢性疼痛状况的一个标志。因此,研究疼痛相关学习中的个体差异具有重要的临床和转化意义。在此,我们开发并进行了外部验证,建立了一种基于静息态脑连接的新型疼痛相关学习预测模型。预先注册的外部验证表明,所提出的模型解释了疼痛相关学习中8%-12%的个体间差异。模型预测由杏仁核、后岛叶、感觉运动、额顶叶和小脑区域的连接驱动,勾勒出一个在厌恶学习和疼痛中通常描述的网络。我们提出所得模型作为临床和转化疼痛研究中一个强大且易于获取的生物标志物候选物,对个性化治疗方法具有潜在的积极影响,并有很大潜力推进我们对疼痛相关学习神经机制的理解。