Karoam Hassan A, Bruss Joel, Champoux Katharine, Lemos Marcelo Delboni, Faillenot Isabelle, Ciampi de Andrade Daniel, Hwang Kai, Bayman Emine, Vaidya Jatin, Gordon Evan M, Tranel Daniel, Geerling Joel C, Boes Aaron D
Interdisciplinary Graduate Program in Neuroscience, University of Iowa Graduate College, Iowa City, IA, United States.
Department of Neurology, University of Iowa Carver College of Medicine, Iowa City, IA, United States.
Pain. 2025 May 9;166(9):e303-e313. doi: 10.1097/j.pain.0000000000003618.
Identifying lesion sites associated with central poststroke pain (CPSP) may facilitate targeted screening for early symptoms, possibly even paving the way for preventive measures and earlier treatment initiation. Here, we test the hypothesis that damage to a nociceptive pathway extending from the brainstem to the cerebral cortex, and including white matter tracts, is associated with CPSP. We investigated the lesion locations of 72 patients with CPSP relative to poststroke comparison subjects without pain (n = 123), divided into a discovery and independent validation data set. The study included three main analyses: (1) we compared lesion intersection with our a priori region of interest (ROI) between groups with and without CPSP, (2) we performed lesion-symptom mapping to evaluate whether lesions associated with CPSP localize to the a priori ROI, and (3) we used lesion network mapping to infer the broader structural and functional connectivity patterns associated with CPSP lesions. CPSP lesions overlapped the nociceptive pathway ROI to a greater extent than comparison lesions. Lesion-symptom mapping identified a CPSP-associated region overlapping with the ventrocaudal thalamus and adjacent white matter, which was located mostly within the a priori ROI. Lesion network mapping demonstrated that lesions associated with CPSP disrupt nodes and tracts of the nociceptive pathway ROI. Interestingly, the CPSP lesion network results demonstrated connectivity to intereffector nodes of the primary motor cortex, providing a novel link between CPSP and the somato-cognitive action network. Together, these findings indicate that CPSP can be conceptualized as a lesion-associated network disruption of the nociceptive pathway and somato-cognitive action network.
识别与中风后中枢性疼痛(CPSP)相关的病变部位可能有助于针对性地筛查早期症状,甚至可能为预防措施和更早开始治疗铺平道路。在此,我们检验了这样一个假设,即从脑干延伸至大脑皮层、包括白质束在内的伤害性通路受损与CPSP相关。我们调查了72例CPSP患者相对于无疼痛的中风后对照受试者(n = 123)的病变位置,分为发现数据集和独立验证数据集。该研究包括三项主要分析:(1)我们比较了有和没有CPSP的两组之间病变与我们的先验感兴趣区域(ROI)的交集,(2)我们进行了病变-症状映射以评估与CPSP相关的病变是否定位于先验ROI,以及(3)我们使用病变网络映射来推断与CPSP病变相关的更广泛的结构和功能连接模式。CPSP病变与伤害性通路ROI的重叠程度大于对照病变。病变-症状映射确定了一个与腹侧尾状丘脑和相邻白质重叠的CPSP相关区域,该区域大多位于先验ROI内。病变网络映射表明,与CPSP相关的病变破坏了伤害性通路ROI的节点和束。有趣的是,CPSP病变网络结果显示与初级运动皮层的效应器间节点有连接,这为CPSP与躯体认知动作网络之间提供了一个新的联系。总之,这些发现表明,CPSP可被概念化为伤害性通路和躯体认知动作网络的病变相关网络破坏。