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与小血管疾病相比,缓慢扩张和非扩张的多发性硬化病变的位移方向和幅度不同。

Direction and magnitude of displacement differ between slowly expanding and non-expanding multiple sclerosis lesions as compared to small vessel disease.

机构信息

Department of Neurology, Neuroinnovation Program, Multiple Sclerosis and Neuroimmunology Imaging Program, The University of Texas Southwestern Medical Center, 5303 Harry Hines Blvd., Dallas, TX, 75390-8806, USA.

Department of Computer Science, University of Texas at Dallas, Dallas, TX, USA.

出版信息

J Neurol. 2022 Aug;269(8):4459-4468. doi: 10.1007/s00415-022-11089-9. Epub 2022 Apr 5.

Abstract

BACKGROUND AND PURPOSE

Differentiating between multiple sclerosis (MS) and small vessel disease (SVD) lesions represents a key challenge in the day-to-day management of patients. We aimed to distinguish between MS and SVD by identifying the dynamics of lesion movement patterns between enlarging and contracting foci from two MRI time points.

METHODS

Standardized 3-Tesla 3-dimensional brain magnetic resonance imaging (MRI) studies were performed at two time points on enrolled MS and SVD patients. Selected supratentorial lesions were segmented and longitudinal changes in the direction of lesion displacement and magnitude along with the evolution of contracting and expanding T1-weighted and T2-weighted MS lesions were quantified based on lesion centroid positioning. Bayesian linear mixed effects regression models were constructed to evaluate associations between changes in lesion transitions and disease state.

RESULTS

A total of 420 lesions were analyzed from 35 MS (female (F):22 (62.9%); median age (range):38 years (y) (22-61), median disease duration:7.38y (0.38-20.99)) and 12 SVD patients (F:11 (100%); 54y (40-66)). MS T2-weighted lesions that increased in volume between MRI time points demonstrated movement toward the cortex (p = 0.01), whereas those that decreased in volume moved toward the center (p < 0.0001). Lesion volume changes related to SVD demonstrated no effect on movement direction over time. Both expanding (p = 0.03) and contracting (p = 0.01) MS lesions demonstrated greater distances between centroids when compared to SVD.

CONCLUSION

Lesion dynamics may reveal distinct characteristics associated with the biology of disease while providing further insights into the behavior of inflammatory CNS disorders.

摘要

背景与目的

在患者日常管理中,区分多发性硬化症(MS)和小血管疾病(SVD)病灶是一项关键挑战。我们旨在通过识别两个 MRI 时间点之间扩大和收缩病灶之间病灶移动模式的动态来区分 MS 和 SVD。

方法

对纳入的 MS 和 SVD 患者进行两次标准的 3 特斯拉 3 维脑磁共振成像(MRI)研究。对选定的幕上病灶进行分割,并根据病灶中心位置的定位,量化病变位移方向和病变大小的纵向变化,以及收缩和扩大 T1 加权和 T2 加权 MS 病变的演变。构建贝叶斯线性混合效应回归模型来评估病变转变与疾病状态之间的变化关系。

结果

共分析了 35 例 MS 患者(女性(F):22 例(62.9%);中位年龄(范围):38 岁(22-61),中位病程:7.38 年(0.38-20.99))和 12 例 SVD 患者(F:11 例(100%);54 岁(40-66))的 420 个病灶。在 MRI 时间点之间体积增加的 MS T2 加权病灶向皮质移动(p=0.01),而体积减少的病灶向中心移动(p<0.0001)。与 SVD 相关的病变体积变化对运动方向没有影响。与 SVD 相比,扩张(p=0.03)和收缩(p=0.01)的 MS 病灶的质心之间距离更大。

结论

病灶动力学可能揭示与疾病生物学相关的独特特征,并为炎症性中枢神经系统疾病的行为提供进一步的见解。

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