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多发性硬化症患者接受芬戈莫德初始治疗后的功能连接性变化

Functional Connectivity Changes After Initial Treatment With Fingolimod in Multiple Sclerosis.

作者信息

Petsas Nikolaos, De Giglio Laura, González-Quintanilla Vicente, Giuliani Manuela, De Angelis Floriana, Tona Francesca, Carmellini Maurizio, Mainero Caterina, Pozzilli Carlo, Pantano Patrizia

机构信息

Department of Radiology, IRCCS NEUROMED, Pozzilli, Italy.

Multiple Sclerosis Centre, Azienda Ospedaliera Sant'Andrea, Rome, Italy.

出版信息

Front Neurol. 2019 Mar 22;10:153. doi: 10.3389/fneur.2019.00153. eCollection 2019.

DOI:10.3389/fneur.2019.00153
PMID:30967828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6438876/
Abstract

On the basis of recent functional MRI studies, Multiple Sclerosis (MS) has been interpreted as a multisystem disconnection syndrome. Compared to normal subjects, MS patients show alterations in functional connectivity (FC). However, the mechanisms underlying these alterations are still debated. The aim of the study is to investigate resting state (RS) FC changes after initial treatment with fingolimod, a proven anti-inflammatory and immunomodulating agent for MS. We studied 32 right-handed relapsing-remitting MS patients (median Expanded Disability Status Scale: 2.0, mean disease duration: 8.8 years) who underwent both functional and conventional MRI with a 3 Tesla magnet. All assessments were performed 3 weeks before starting fingolimod, then, at therapy-initiation stage and at month 6. Each imaging session included scans at baseline (run1) and after (run2) a 25-min, within-session, motor-practice task, consisting of a paced right-thumb flexion. FC was assessed using a seed on the left primary motor cortex to obtain parametric maps at run1 and task-induced FC change (run2-run1). Comparison between 3-week before- and fingolimod start sessions accounted for a test-retest effect. The main outcome was the changes in both baseline and task-induced changes in FC, between initiation and 6 months. MRI contrast enhancement was detected in 14 patients at initiation and only in 3 at month 6. There was a significant improvement ( < 0.05) in cognitive function, as measured by the Paced Auditory Serial Addition Task, at month 6 compared to initiation. After accounting for test-retest effect, baseline FC significantly decreased at month 6, with respect to initiation ( < 0.05, family-wise error corrected) in bilateral occipito-parietal areas and cerebellum. A task-induced change in FC at month 6 showed a significant increment in all examined sessions, involving not only areas of the sensorimotor network, but also posterior cortical areas (cuneus and precuneus) and areas of the prefrontal and temporal cortices ( < 0.05, family-wise error corrected). Cognitive improvement at month 6 was significantly ( < 0.05) related to baseline FC reduction in posterior cortical areas. This study shows significant changes in functional connectivity, both at baseline and after the execution of a simple motor task following 6 months of fingolimod therapy.

摘要

基于近期的功能磁共振成像研究,多发性硬化症(MS)被解释为一种多系统连接障碍综合征。与正常受试者相比,MS患者的功能连接性(FC)出现改变。然而,这些改变背后的机制仍存在争议。本研究的目的是调查用芬戈莫德(一种已证实的用于治疗MS的抗炎和免疫调节药物)进行初始治疗后静息状态(RS)FC的变化。我们研究了32名右利手复发缓解型MS患者(扩展残疾状态量表中位数:2.0,平均病程:8.8年),他们使用3特斯拉磁体进行了功能磁共振成像和传统磁共振成像检查。所有评估均在开始使用芬戈莫德前3周、治疗起始阶段和第6个月时进行。每次成像检查包括在基线(run1)和25分钟的组内运动练习任务(由有节奏的右拇指屈曲组成)后(run2)进行扫描。使用左侧初级运动皮层上的一个种子点来评估FC,以获得run1时的参数图和任务诱导的FC变化(run2 - run1)。在开始使用芬戈莫德前3周和开始使用芬戈莫德时的检查之间的比较考虑了重测效应。主要结果是在起始阶段和6个月之间基线和任务诱导的FC变化。在起始阶段,14名患者检测到磁共振成像对比增强,而在第6个月时只有3名患者检测到。与起始阶段相比,在第6个月时,通过听觉连续加法任务测量的认知功能有显著改善(<0.05)。在考虑重测效应后,与起始阶段相比,第6个月时双侧枕顶叶区域和小脑的基线FC显著降低(<0.05,家族性错误校正)。第6个月时任务诱导的FC变化在所有检查的阶段均显示出显著增加,不仅涉及感觉运动网络区域,还涉及后皮质区域(楔叶和楔前叶)以及前额叶和颞叶皮质区域(<0.05,家族性错误校正)。第6个月时的认知改善与后皮质区域基线FC降低显著相关(<0.05)。本研究表明,在芬戈莫德治疗6个月后,无论是基线还是在执行简单运动任务后,功能连接性都有显著变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/b23d7429c394/fneur-10-00153-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/bfa488c8b54b/fneur-10-00153-g0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/ce6e0bd51b8f/fneur-10-00153-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/a34a17c7b830/fneur-10-00153-g0006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/5d0bbdaf7d97/fneur-10-00153-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/a9c0efa3fd66/fneur-10-00153-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/d8483b86f5b8/fneur-10-00153-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/ce6e0bd51b8f/fneur-10-00153-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/a34a17c7b830/fneur-10-00153-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a08a/6438876/b23d7429c394/fneur-10-00153-g0007.jpg

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