Multimodal investigation of neuropathic pain mechanisms in focal spinal lesions.

IF 1.6 Q4 CLINICAL NEUROLOGY
Scandinavian Journal of Pain Pub Date : 2026-06-19 eCollection Date: 2026-01-01 DOI:10.1515/sjpain-2025-0065
Paulina S Scheuren, Gergely David, John L K Kramer, Catherine R Jutzeler, Markus Hupp, Patrick Freund, Walter Magerl, Armin Curt, Michèle Hubli, Jan Rosner
{"title":"Multimodal investigation of neuropathic pain mechanisms in focal spinal lesions.","authors":"Paulina S Scheuren, Gergely David, John L K Kramer, Catherine R Jutzeler, Markus Hupp, Patrick Freund, Walter Magerl, Armin Curt, Michèle Hubli, Jan Rosner","doi":"10.1515/sjpain-2025-0065","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Focal spinal cord lesions occur across a variety of neurological diseases including non-traumatic cervical myelopathies which can lead to neuropathic pain. Currently, the degree to which signs and symptoms of neuropathic pain correlate with functional impairments and/or anatomical deficits remains unclear. This study aimed to identify structural and functional determinants associated with neuropathic pain in individuals with focal spinal lesions.</p><p><strong>Methods: </strong>Individuals fulfilling the diagnostic criteria of neuropathic pain were identified among individuals with cervical myelopathy presenting with focal spinal lesions. Lesion volume and the extent of structural damage affecting the spinothalamic tract, dorsal columns, dorsal horn, and ventral horn were evaluated with tract-specific MRI of the cervical spinal cord. Quantitative sensory testing (QST) (i.e., thermal/mechanical thresholds) was performed at the most affected skin area. Additionally, contact heat-evoked potentials (CHEPs) were acquired following stimulation at the most affected skin area to objectively assess the functional integrity of the spinothalamic tract.</p><p><strong>Results: </strong>MRI-derived structural damage was similar for individuals with (n=8) and without (n=8) neuropathic pain in all regions of interest (p>0.05). Mechanical hyperalgesia upon QST was observed in both groups. However, functional preservation of the spinothalamic system, measured by CHEPs, was present in 87 % of individuals with neuropathic pain, compared to 38 % of pain-free individuals (p=0.039).</p><p><strong>Conclusions: </strong>These observations suggest that segmental hyperexcitability resulting from structural spinal cord damage, in combination with residual sparing of spinothalamic afferents, may represent a key pathophysiological constellation contributing to central neuropathic pain following focal spinal lesions.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"26 1","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2026-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scandinavian Journal of Pain","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/sjpain-2025-0065","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: Focal spinal cord lesions occur across a variety of neurological diseases including non-traumatic cervical myelopathies which can lead to neuropathic pain. Currently, the degree to which signs and symptoms of neuropathic pain correlate with functional impairments and/or anatomical deficits remains unclear. This study aimed to identify structural and functional determinants associated with neuropathic pain in individuals with focal spinal lesions.

Methods: Individuals fulfilling the diagnostic criteria of neuropathic pain were identified among individuals with cervical myelopathy presenting with focal spinal lesions. Lesion volume and the extent of structural damage affecting the spinothalamic tract, dorsal columns, dorsal horn, and ventral horn were evaluated with tract-specific MRI of the cervical spinal cord. Quantitative sensory testing (QST) (i.e., thermal/mechanical thresholds) was performed at the most affected skin area. Additionally, contact heat-evoked potentials (CHEPs) were acquired following stimulation at the most affected skin area to objectively assess the functional integrity of the spinothalamic tract.

Results: MRI-derived structural damage was similar for individuals with (n=8) and without (n=8) neuropathic pain in all regions of interest (p>0.05). Mechanical hyperalgesia upon QST was observed in both groups. However, functional preservation of the spinothalamic system, measured by CHEPs, was present in 87 % of individuals with neuropathic pain, compared to 38 % of pain-free individuals (p=0.039).

Conclusions: These observations suggest that segmental hyperexcitability resulting from structural spinal cord damage, in combination with residual sparing of spinothalamic afferents, may represent a key pathophysiological constellation contributing to central neuropathic pain following focal spinal lesions.

脊髓局灶性病变神经性疼痛机制的多模式研究。
目的:局灶性脊髓病变发生在各种神经系统疾病中,包括可导致神经性疼痛的非创伤性颈脊髓病。目前,神经性疼痛的体征和症状与功能损伤和/或解剖缺陷的关联程度尚不清楚。本研究旨在确定与局灶性脊柱病变患者神经性疼痛相关的结构和功能决定因素。方法:在出现局灶性脊髓病变的颈脊髓病患者中,确定符合神经性疼痛诊断标准的个体。病变体积和影响脊髓丘脑束、背柱、背角和腹角的结构损伤程度通过颈脊髓束特异性MRI进行评估。定量感官测试(QST)(即热/机械阈值)在受影响最严重的皮肤区域进行。此外,在受影响最严重的皮肤区域进行刺激后获得接触热诱发电位(CHEPs),以客观评估脊髓丘脑束的功能完整性。结果:在所有感兴趣的区域,有(n=8)和没有(n=8)神经性疼痛的个体,mri衍生的结构损伤相似(p>0.05)。两组均观察到QST后的机械性痛觉过敏。然而,chep测量的脊髓丘脑系统功能保存存在于87% %的神经性疼痛患者中,而无痛患者为38% % (p=0.039)。结论:这些观察结果表明,由脊髓结构性损伤引起的节段性高兴奋性,加上脊髓丘脑传入神经的残余保留,可能是导致局灶性脊髓病变后中枢神经性疼痛的关键病理生理因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Scandinavian Journal of Pain
Scandinavian Journal of Pain CLINICAL NEUROLOGY-
CiteScore
3.30
自引率
6.20%
发文量
73
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书