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多发性硬化症所致病灶性萎缩的时间进程。

Time course of lesion-induced atrophy in multiple sclerosis.

机构信息

Buffalo Neuroimaging Analysis Center, Department of Neurology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA.

Jacobs Multiple Sclerosis Center, Department of Neurology, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA.

出版信息

J Neurol. 2022 Aug;269(8):4478-4487. doi: 10.1007/s00415-022-11094-y. Epub 2022 Apr 8.

Abstract

BACKGROUND AND PURPOSE

White matter (WM) tract disruption impacts volume loss in connected deep gray matter (DGM) over 5 years in people with multiple sclerosis (PwMS). However, the timeline of this phenomenon remains poorly characterized.

MATERIALS AND METHODS

Annual serial MRI for 181 PwMS was retrospectively analyzed from a 10-year clinical trial database. Annualized thalamic atrophy, DGM atrophy, and disruption of connected WM tracts were measured. For time series analysis, ~700 epochs were collated using a sliding 5-year window, and regression models predicting 1-year atrophy were applied to characterize the influence of new tract disruption from preceding years, while controlling for whole brain atrophy and other relevant factors.

RESULTS

Disruptions of WM tracts connected to the thalamus were significantly associated with thalamic atrophy 1 year later (β: 0.048-0.103). This effect was not observed for thalamic tract disruption concurrent with the time of atrophy nor for thalamic tract disruption preceding the atrophy by 2-4 years. Similarly, disruptions of white matter tracts connected to the DGM were significantly associated with DGM atrophy 1 year later (β: 0.078-0.111), but not for tract disruption concurrent with, nor preceding the atrophy by 2-4 years.

CONCLUSION

Increased rates of thalamic and DGM atrophy were restricted to 1 year following newly developed disruption in connected WM tracts. In research and clinical settings, additional gray matter atrophy may be expected 1 year following new lesion growth in connected white matter.

摘要

背景与目的

在多发性硬化症患者(PwMS)中,白质(WM)束中断会影响 5 年内与深部灰质(DGM)相连的体积损失。然而,这种现象的时间进程仍未得到很好的描述。

材料与方法

对一项为期 10 年的临床试验数据库中的 181 例 PwMS 的年度连续 MRI 进行回顾性分析。测量了每年的丘脑萎缩、DGM 萎缩和连接 WM 束的中断情况。为了进行时间序列分析,使用滑动 5 年窗口整理了大约 700 个时间点,并应用回归模型预测 1 年的萎缩情况,以描述前几年新的 WM 束中断对随后 1 年萎缩的影响,同时控制全脑萎缩和其他相关因素。

结果

与丘脑相连的 WM 束中断与 1 年后的丘脑萎缩显著相关(β:0.048-0.103)。与同时发生的丘脑束中断或在萎缩前 2-4 年发生的丘脑束中断相比,这种效应并不明显。同样,与 DGM 相连的 WM 束中断与 1 年后的 DGM 萎缩显著相关(β:0.078-0.111),但与同时发生的或在萎缩前 2-4 年发生的 DGM 束中断无关。

结论

在新的连接性 WM 束中断后,丘脑和 DGM 萎缩的速度加快仅局限于 1 年。在研究和临床环境中,在与 WM 相关的新病变生长后,预计会有额外的灰质萎缩在 1 年后出现。

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