Igawa Yuki, Osumi Michihiro, Takamura Yusaku, Uchisawa Hidekazu, Iki Shinya, Fuchigami Takeshi, Uragami Shinji, Nishi Yuki, Mori Nobuhiko, Hosomi Koichi, Morioka Shu
Graduate School of Health Science, Kio University, Kitakatsuragi-gun, Nara 635-0832, Japan.
Department of Rehabilitation Medicine, Nishiyamato Rehabilitation Hospital, Kitakatsuragi-gun, Nara 639-0218, Japan.
Brain Commun. 2025 Apr 30;7(3):fcaf128. doi: 10.1093/braincomms/fcaf128. eCollection 2025.
Post-stroke pain is heterogeneous and includes both nociceptive and neuropathic pain. These subtypes can be comprehensively assessed using several clinical tools, such as pain-related questionnaires, quantitative somatosensory tests and brain imaging. In the present study, we conducted a comprehensive assessment of patients with central post-stroke pain and non-central post-stroke pain and analysed their clinical features. We also performed a detailed analysis of the relationships between brain lesion areas or structural disconnection of the white matter and somatosensory dysfunctions. In this multicentre cross-sectional study, 70 patients were divided into 24 with central post-stroke pain, 26 with non-central post-stroke pain and 20 with no-pain groups. Multiple logistic regression analysis was used to summarize the relationships between each pathological feature (for the central post-stroke pain and non-central post-stroke pain groups) and pain-related factors or the results of quantitative somatosensory tests. Relationships between somatosensory dysfunctions and brain lesion areas were analysed using voxel-based lesion-symptom mapping and voxel-based disconnection-symptom mapping. All pathology feature models indicated that central post-stroke pain was associated with cold hypoesthesia at 8°C (β = 2.98, odds ratio = 19.6, 95% confidence interval = 2.7-141.8), cold hyperalgesia at 8°C (β = 2.61, odds ratio = 13.6, 95% confidence interval = 1.13-163.12) and higher Neuropathic Pain Symptom Inventory scores (for spontaneous and evoked pain items only; β = 0.17, odds ratio = 1.19, 95%, confidence interval = 1.07-1.32), whereas non-central post-stroke pain was associated with joint pain (β = 5.01, odds ratio = 149.854, 95%, confidence interval = 19.93-1126.52) and lower Neuropathic Pain Symptom Inventory scores (β = -0.17, odds ratio = 0.8, 95%, confidence interval = 0.75-0.94). In the voxel-based lesion-symptom mapping, the extracted lesion areas indicated mainly voxels significantly associated with cold hyperalgesia, allodynia at 8°C and 22°C and heat hypoesthesia at 45°C. These extracted areas were mainly in the putamen, insular cortex, hippocampus, Rolandic operculum, retrolenticular part of internal and external capsules and sagittal stratum. In voxel-based disconnection-symptom mapping, the extracted disconnection maps were significantly associated with cold hyperalgesia at 8°C, and heat hypoesthesia at 37°C and 45°C. These structural disconnection patterns were mainly in the cingulum frontal parahippocampal tract, the reticulospinal tract and the superior longitudinal fasciculus with a widespread interhemispheric disconnection of the corpus callosum. These findings serve as important indicators to facilitate decision-making and optimize precision treatments through data dimensionality reduction when diagnosing post-stroke pain using clinical assessments, such as bedside quantitative sensory testing, pain-related factors, pain questionnaires and brain imaging.
中风后疼痛具有异质性,包括伤害性疼痛和神经性疼痛。这些亚型可以使用多种临床工具进行全面评估,如疼痛相关问卷、定量体感测试和脑成像。在本研究中,我们对中风后中枢性疼痛和非中枢性疼痛患者进行了全面评估,并分析了他们的临床特征。我们还详细分析了脑损伤区域或白质结构连接中断与体感功能障碍之间的关系。在这项多中心横断面研究中,70名患者被分为24名中风后中枢性疼痛患者、26名中风后非中枢性疼痛患者和20名无疼痛组。采用多因素逻辑回归分析总结各病理特征(中风后中枢性疼痛组和中风后非中枢性疼痛组)与疼痛相关因素或定量体感测试结果之间的关系。使用基于体素的损伤-症状映射和基于体素的连接中断-症状映射分析体感功能障碍与脑损伤区域之间的关系。所有病理特征模型均表明,中风后中枢性疼痛与8°C时的冷觉减退(β = 2.98,优势比 = 19.6,95%置信区间 = 2.7 - 141.8)、8°C时的冷觉过敏(β = 2.61,优势比 = 13.6,95%置信区间 = 1.13 - 163.12)以及更高的神经性疼痛症状量表评分(仅针对自发痛和诱发性疼痛项目;β = 0.17,优势比 = 1.19,95%置信区间 = 1.07 - 1.32)相关,而中风后非中枢性疼痛与关节疼痛(β = 5.01,优势比 = 149.854,95%置信区间 = 19.93 - 1126.52)和更低的神经性疼痛症状量表评分(β = -0.17,优势比 = 0.8,95%置信区间 = 0.75 - 0.94)相关。在基于体素的损伤-症状映射中,提取的损伤区域主要显示为与8°C时的冷觉过敏、8°C和22°C时的痛觉过敏以及45°C时的热觉减退显著相关的体素。这些提取区域主要位于壳核、岛叶皮质、海马、中央沟盖、内囊和外囊的豆状核后部以及矢状层。在基于体素的连接中断-症状映射中,提取的连接中断图与8°C时的冷觉过敏以及37°C和45°C时的热觉减退显著相关。这些结构连接中断模式主要位于扣带前海马旁束、网状脊髓束和上纵束,胼胝体存在广泛的半球间连接中断。这些发现是重要指标,有助于在使用临床评估(如床边定量感觉测试、疼痛相关因素、疼痛问卷和脑成像)诊断中风后疼痛时,通过数据降维来促进决策制定并优化精准治疗。