Buzhanskyy Andriy, Duarte Isabel Catarina, Patto Assunção Vaz, Donato Helena, Castelo-Branco Miguel, Abejas Abel, Lapa Teresa
Faculty of Health Sciences, Universidade da Beira Interior, Av. Infante D. Henrique, Covilhã, 6200-506, Portugal.
Coimbra Institute for Biomedical Imaging and Translational Research (CIBIT), Institute of Nuclear Sciences Applied to Health (ICNAS), University of Coimbra, R. Santa Comba, Coimbra, 3000-548, Portugal.
Curr Pain Headache Rep. 2025 Jan 30;29(1):43. doi: 10.1007/s11916-024-01339-y.
Central Post-Stroke Pain (CPSP) is a debilitating condition with a significant prevalence in stroke survivors. Set apart by its refractory to treatment neuropathic pain, it appears to arise from lesions in the spino-thalamo-cortical pathways, particularly in the thalamus. Despite advances in neuroimaging techniques, the pathophysiology of CPSP remains poorly understood, with limited diagnostic criteria and therapeutic approaches.
This systematic review aims to identify neuroimaging markers associated with CPSP, establish correlations between brain lesions and CPSP development, and explore the utility of neuroimaging techniques for diagnosis and prognosis. Secondary objectives involve establishing a link between CPSP and secondary brain area lesions and what type of pain patients with CPSP are more likely to experience.
A systematic review was conducted following PRISMA guidelines. Relevant articles were sourced from PubMed, Embase, and Web of Science, using a predefined search strategy targeting CPSP and neuroimaging studies (MRI, PET, SPECT). Studies involving adult CPSP patients with post-stroke neuroimaging were included. Data from 14 studies was analyzed, focusing on lesion locations, neuroimaging findings, and functional connectivity. Risk of bias was assessed using the QUADAS-2 tool.
Key findings highlighted the association of CPSP with lesions in the ventral posterolateral and the ventral medial nuclei of the thalamus, spinothalamic pathway, and cortical areas like the insula and operculum. Functional connectivity studies highlighted the role of disrupted neural networks in pain perception. Limitations in the reviewed studies included small sample sizes, selection bias, and heterogeneity in study designs.
Neuroimaging findings confirm the significance of thalamic and spinothalamic pathway lesions in CPSP pathophysiology. Despite these insights, gaps in research underline the need for larger, multicenter trials to identify reliable biomarkers for diagnosis and therapeutic targets. Advanced neuroimaging combined with machine learning could be the key to understanding and managing CPSP.
中风后中枢性疼痛(CPSP)是一种使人衰弱的病症,在中风幸存者中具有相当高的发病率。它以难治性神经性疼痛为特征,似乎源于脊髓丘脑皮质通路的损伤,尤其是丘脑的损伤。尽管神经成像技术取得了进展,但CPSP的病理生理学仍知之甚少,诊断标准和治疗方法有限。
本系统评价旨在识别与CPSP相关的神经成像标志物,建立脑损伤与CPSP发生之间的相关性,并探索神经成像技术在诊断和预后方面的效用。次要目的包括建立CPSP与继发性脑区损伤之间的联系,以及CPSP患者更可能经历何种类型的疼痛。
按照PRISMA指南进行系统评价。使用针对CPSP和神经成像研究(MRI、PET、SPECT)的预定义搜索策略,从PubMed、Embase和科学网获取相关文章。纳入涉及成年CPSP患者中风后神经成像的研究。分析了14项研究的数据,重点关注损伤部位、神经成像结果和功能连接性。使用QUADAS-2工具评估偏倚风险。
主要发现突出了CPSP与丘脑腹后外侧核和腹内侧核、脊髓丘脑通路以及岛叶和脑盖等皮质区域损伤之间的关联。功能连接性研究强调了神经网络中断在疼痛感知中的作用。所审查研究的局限性包括样本量小、选择偏倚和研究设计的异质性。
神经成像结果证实了丘脑和脊髓丘脑通路损伤在CPSP病理生理学中的重要性。尽管有这些见解,但研究中的差距凸显了需要进行更大规模的多中心试验,以识别用于诊断的可靠生物标志物和治疗靶点。先进的神经成像与机器学习相结合可能是理解和管理CPSP的关键。