Lesion and Disconnection Profiles of Pain Quality Subtypes After Stroke: Implications for Prognosis and Rehabilitation.

IF 3.4 2区 医学 Q1 ANESTHESIOLOGY
Shinji Uragami, Yuki Igawa, Yusaku Takamura, Shinya Iki, Shu Morioka, Michihiro Osumi
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引用次数: 0

Abstract

Background: Post-stroke pain (PSP) presents with diverse pain qualities. However, the structural brain correlates underlying these distinct pain qualities remains poorly understood.

Methods: We analysed PSP patients using clinical assessments, clustering based on pain qualities assessed using the Neuropathic Pain Symptom Inventory, longitudinal pain intensity evaluation and brain lesion/disconnection mapping (computed tomography/magnetic resonance imaging and Bayesian lesion-deficit inference). Pain quality-based clusters and their corresponding lesion sites and white matter tracts were identified.

Results: We analysed 114 PSP patients. Cluster analysis using pain qualities classified patients into four distinct subgroups: CL1 (cold-evoked/tingling), CL2 (deep squeezing/pressure), CL3 (tingling) and CL4 (pressure-evoked). CL1 and CL3 patients predominantly exhibited features of central post-stroke pain, characterised by sensory disturbances such as allodynia and numbness. Lesion mapping revealed involvement of the thalamus, putamen and posterior insula. Disconnection analysis identified the superior thalamic radiation (Bayes factor > 70) as a common white matter tract. In contrast, CL2 and CL4 were characterised by musculoskeletal-type pain associated with joint pain, restricted range of motion and higher motor impairment. Lesions in these groups were mainly localised to the frontal lobe, with disconnection of the corticospinal and fronto-aslant tracts (Bayes factor > 50). Longitudinal analysis demonstrated pain intensity decreased over time across all clusters, with a trend towards slower improvement in Cluster 3.

Conclusions: Pain quality reflects distinct pathological mechanisms of PSP and may be associated with specific patterns of brain lesions and white matter disconnections and rehabilitation prognosis. Identifying pain-quality subtypes may help inform outcomes and guide personalised rehabilitation.

Significance statement: By linking distinct pain qualities with lesion and disconnection profiles, this study clarifies the neural mechanisms underlying post-stroke pain. Identifying these pain-quality subtypes provides insights into prognosis and supports the development of personalized rehabilitation strategies tailored to specific pain mechanisms.

脑卒中后疼痛质量亚型的病变和断开概况:对预后和康复的影响。
背景:卒中后疼痛(PSP)表现为不同的疼痛特征。然而,这些不同的疼痛特征背后的大脑结构相关性仍然知之甚少。方法:我们使用临床评估、基于神经性疼痛症状量表评估疼痛质量的聚类、纵向疼痛强度评估和脑损伤/断开映射(计算机断层扫描/磁共振成像和贝叶斯损伤-缺陷推断)对PSP患者进行分析。以疼痛质量为基础的簇及其相应的病变部位和白质束被识别。结果:我们分析了114例PSP患者。利用疼痛质量的聚类分析将患者分为四个不同的亚组:CL1(冷诱发/刺痛)、CL2(深挤压/压力)、CL3(刺痛)和CL4(压力诱发)。CL1和CL3患者主要表现为中枢性卒中后疼痛,以感觉障碍为特征,如异常性疼痛和麻木。病变图显示丘脑、壳核和脑岛后部受累。断开分析发现丘脑上辐射(贝叶斯因子bbb70)是一个共同的白质束。相比之下,CL2和CL4的特征是肌肉骨骼型疼痛,伴有关节疼痛,活动范围受限和较高的运动障碍。这些组的病变主要局限于额叶,皮质脊髓束和额斜束断开(贝叶斯因子bbb50)。纵向分析表明,疼痛强度随时间的推移在所有组中都有所下降,在第3组中有缓慢改善的趋势。结论:疼痛质量反映了PSP的不同病理机制,并可能与脑损伤和白质断开的特定模式和康复预后有关。识别疼痛质量亚型可能有助于告知结果并指导个性化康复。意义声明:通过将不同的疼痛特征与损伤和断连特征联系起来,本研究阐明了脑卒中后疼痛的神经机制。识别这些疼痛质量亚型提供了对预后的见解,并支持针对特定疼痛机制量身定制的个性化康复策略的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Journal of Pain
European Journal of Pain 医学-临床神经学
CiteScore
7.50
自引率
5.60%
发文量
163
审稿时长
4-8 weeks
期刊介绍: European Journal of Pain (EJP) publishes clinical and basic science research papers relevant to all aspects of pain and its management, including specialties such as anaesthesia, dentistry, neurology and neurosurgery, orthopaedics, palliative care, pharmacology, physiology, psychiatry, psychology and rehabilitation; socio-economic aspects of pain are also covered. Regular sections in the journal are as follows: • Editorials and Commentaries • Position Papers and Guidelines • Reviews • Original Articles • Letters • Bookshelf The journal particularly welcomes clinical trials, which are published on an occasional basis. Research articles are published under the following subject headings: • Neurobiology • Neurology • Experimental Pharmacology • Clinical Pharmacology • Psychology • Behavioural Therapy • Epidemiology • Cancer Pain • Acute Pain • Clinical Trials.
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