医学
幻肢
功能连接
幻肢痛
神经科学
物理医学与康复
功能磁共振成像
成像体模
心理学
截肢
放射科
外科
作者
Bixin Zheng,Yan Yin,Hong Xiao,Su Lui,Chuanbing Wen,Yuee Dai,Guang Yang,Jin Liu,Qiyong Gong
出处
期刊:Pain Practice
[Wiley]
日期:2020-11-17
卷期号:21 (4): 394-403
被引量:19
摘要
Abstract Objectives Functional neuroimaging studies have shown that amputees have altered cortical reorganization and functional connectivity (FC). This study aimed to investigate whether patients with phantom limb pain (PLP) and PLP‐free lower limb amputees exhibit changes in corresponding primary cortical motor area/somatosensory cortex (M1/S1) cortical reorganization and supplementary motor area (SMA) network FC. The association between functional magnetic resonance imaging (fMRI) changes and clinical parameters is also explored. Methods A total of 10 PLP patients were matched with 10 PLP‐free amputees and 10 healthy controls (HCs). Before undergoing fMRI, all participants completed questionnaires evaluating pain, anxiety, depression, and health‐related quality of life. Task‐related activation and regions of interest (ROI)‐wise connectivity analysis were applied to differentiate the brain regions of amputees from those of HCs. Linear correlation analysis was used to evaluate the correlation between altered FC and clinical manifestations. Results As compared with HCs, PLP patients showed increased cortical activation in M1/S1 when moving the intact foot, imagining phantom big toe movement, or having the corresponding thumb stimulated. The increased FC in the SMA network included the SMA‐caudate nucleus, SMA‐bilateral insula, and SMA‐anterior cingulate cortex. Furthermore, results of the linear correlation analysis demonstrated that this increased FC was positively correlated with VAS scores, negatively correlated with Medical Outcomes Study 36‐item Short‐Form (SF‐36) scores, and not correlated with anxiety or depression scores. Conclusions Phantom limb pain in lower limb amputees is associated with M1/S1 cortical reorganization and altered SMA network FC in different areas of the brain, which could help to support our understanding of the central mechanism of PLP.
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