小脑上足萎缩可预测伴有小脑症状的复发缓解型多发性硬化症患者的认知障碍:一项DTI研究

G. Nicoletti, P. Valentino, C. Chiriaco, A. Granata, S. Barone, E. Filippelli, M. Caligiuri, B. Vescio, A. Sarica, A. Quattrone
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引用次数: 2

摘要

背景:使用弥散张量成像(DTI),我们验证了小脑分数各向异性(FA)异常可能参与复发-缓解(RR)-多发性硬化症(MS)认知功能障碍的假设。目的:本研究旨在探讨MS中前馈和反馈通路与皮质区连接的区域,即小脑上小脑蒂(SCP)、小脑中小脑蒂(MCP)、齿状核(DN)和丘脑(Th)的微观结构完整性。患者和方法:我们研究了46例RR-MS患者(有小脑体征21例,无小脑体征25例)和23例正常人。所有受试者都进行了认知测试。结果:在小脑型患者中,所有考虑域的认知表现与SCP (r=0.119 ~ 0.735)和丘脑(r=0.477 ~ 0.602)异常从中度到强相关(p<0.05)。讨论:我们的研究显示认知测试与小脑MS患者SCP和丘脑的FA值有重要的相关性。我们不仅发现了丘脑的参与,还发现了作为小脑核和丘脑之间重要联系的SCP的参与,这表明丘脑之外也存在断开。这些结果表明,SCP和丘脑损伤是MS神经退行性小脑过程的临床相关生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Superior Cerebellar Peduncle Atrophy Predicts Cognitive Impairment in Relapsing Remitting Multiple Sclerosis Patients with Cerebellar Symptoms: A DTI Study
Background: Using Diffusion Tensor Imaging (DTI), we tested the hypothesis that cerebellar abnormalities in fractional anisotropy (FA) may be involved in cognitive dysfunctions in Relapsing-Remitting (RR)-Multiple Sclerosis (MS). Objective: The aim of our study was to investigate the microstructural integrity in MS of regions that connect in both feedforward and feedback pathways to cortical areas, i.e., Superior Cerebellar Peduncles (SCP), Middle Cerebellar Peduncles (MCP), Dentate nuclei (DN) and Thalamus (Th). Patients and methods: We studied 46 patients with RR-MS (21 with cerebellar signs and 25 without) and 23 normal subjects. All subjects underwent cognitive testing. Results: In patients with a cerebellar phenotype, cognitive performance in all considered domains was from moderately to strongly related (p<0.05) to abnormalities of SCP (r=0.119 to 0.735) and Thalamus (r=0.477 to 0.602). Discussion: Our study showed an important correlation between cognitive testing and FA values of SCP and thalamus in cerebellar MS patients. We found not only the involvement of thalamus but also of SCP that is an important link between cerebellar nuclei and thalamus, suggesting that a disconnection is present also out of the thalamus. These results suggest that SCP and thalamic damage is a clinically relevant biomarker of the neurodegenerative cerebellar process in MS.
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