Achiron Anat, Warszawer Yehuda, Nissan Yael, Kerpel Ariel, Hoffmann Chen, Harari Gil, Magalashvili David, Tal Sigal
Multiple Sclerosis Center, Sheba Medical Center, Ramat-Gan, Israel.
Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Mult Scler. 2025 May;31(6):689-695. doi: 10.1177/13524585251313749. Epub 2025 Jan 27.
Measuring brain volume changes over time is an objective and dependable surrogate marker for the pathological processes that damage the brain in relapsing-remitting multiple sclerosis (RRMS). These measures are particularly valuable for monitoring the long-term impact of immunomodulatory treatments such as cladribine.
To evaluate the long-term impact of oral cladribine treatment on brain volume loss in patients with RRMS.
This real-world study processed magnetic resonance imaging (MRI) scans using FreeSurfer's recon-all-clinical pipeline leveraging SynthSeg for brain segmentation. Piecewise linear regression was used to analyze brain atrophy changes over 4.5 years before and after cladribine treatment and estimate the time breakpoint of atrophy rate change.
A total of 448 MRI exams from 102 RRMS patients were analyzed. Before the initiation of cladribine treatment, brain atrophy rates were significantly steep with an α1 slope between -1.27 and -0.62 for the Thalamus, DGM, Subcortical GM, Cerebral WM, and BP. Over 2 years after treatment, breakpoints marked a shift in atrophy rates, with post-breakpoint slopes (α2) becoming non-significant, reflecting stabilization of brain atrophy.
Cladribine treatment in highly active RRMS patients protects the brain from atrophy, with stabilization occurring over 2 years after initiation. The extended observation period highlights its sustained benefits compared with shorter clinical trials.
测量脑容量随时间的变化是复发缓解型多发性硬化症(RRMS)中损害大脑的病理过程的客观且可靠的替代标志物。这些测量对于监测免疫调节治疗(如克拉屈滨)的长期影响特别有价值。
评估口服克拉屈滨治疗对RRMS患者脑容量损失的长期影响。
这项真实世界研究使用FreeSurfer的recon-all临床流程处理磁共振成像(MRI)扫描,利用SynthSeg进行脑部分割。采用分段线性回归分析克拉屈滨治疗前后4.5年内的脑萎缩变化,并估计萎缩率变化的时间断点。
共分析了102例RRMS患者的448次MRI检查。在开始使用克拉屈滨治疗前,脑萎缩率显著陡峭,丘脑、深部灰质核团(DGM)、皮质下灰质、脑白质和脑干(BP)的α1斜率在-1.27至-0.62之间。治疗2年后,断点标志着萎缩率的转变,断点后斜率(α2)变得不显著,反映了脑萎缩的稳定。
在高度活跃的RRMS患者中,克拉屈滨治疗可保护大脑免受萎缩,在开始治疗2年后出现稳定。与较短的临床试验相比,延长的观察期突出了其持续的益处。