对急性和慢性多发性硬化症顺磁边缘病变的纵向多参数定量 MRI 评估

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Ahmed M Elkady, Colm Elliott, Dumitru Fetco, David Araujo, Zahra Karimaghaloo, Marco Ganzetti, David Clayton, Licinio Craveiro, Agne Kazlauskaite, Sridar Narayanan, Douglas L Arnold, David A Rudko
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引用次数: 0

摘要

背景:多发性硬化症(MS)顺磁性边缘病变(PRLs)是慢性活动性生物标志物,表现出复杂的铁和髓鞘变化,这可能使传统 MRI 方法的量化变得复杂:研究类型:回顾性/纵向研究:研究类型:回顾性/纵向研究。受试者:95名进展期多发性硬化症受试者,他们至少有一个持续性PRL,并参加了CONSONANCE试验:3-T/感度加权、T1加权、T2加权和液体衰减反转恢复:在筛查、24、48 和 96 周时使用定量磁感应强度 (QS)、R2* 和标准化 T1w/T2w 比值 (sT1w/T2w) 测量急性/慢性 PRL 和非 PRL。对整个病灶、核心和边缘进行了 PRL 分析。评估了 PRL 核心和边缘 sT1w/T2w、QS 和 R2* 之间的相关性:线性混合模型。A P值 结果:与筛查时的非PRL相比,通过对慢性PRL进行全组织分析,sT1w/T2w(-0.24 ± -5.3 × 10-3)和R2*(-3.6 ± 2.2 Hz)明显下降,但QS(+21 ± 1.3 ppb)明显上升。与急性/慢性非 PRL 相比,急性/慢性 PRL 在 96 周时间点累积的组织损伤更为明显(ΔsT1w/T2w = -0.21/-0.24 ± 0.033/0.0053;ΔR2* = -4.4/-3.6 ± 1.4/2.2 Hz)。新的急性PRL sT1w/T2w在病变开始后24周在病变核心(+4.3 × 10-3 ± 1.2 × 10-4)和边缘(+5.6 × 10-3 ± 1.2 × 10-4)显著增加,提示部分恢复。相反,慢性 PRL 在最初的 24 周内,核心(-2.1 × 10-4 ± 2.0 × 10-5)和边缘(-2.4 × 10-4 ± 2.0 × 10-5)的 sT1w/T2w 均显著下降,表明组织损伤不可逆转。在 PRL 核心和边缘 sT1w/T2w (R2 = 0.53)、R2* (R2 = 0.69) 和 QS (R2 = 0.52) 之间观察到显著的正相关:数据结论:PRL的多参数评估有可能成为评估进展期多发性硬化症患者慢性活动性PRL中复杂的铁和髓鞘变化的重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Longitudinal Multiparametric Quantitative MRI Evaluation of Acute and Chronic Multiple Sclerosis Paramagnetic Rim Lesions.

Background: Multiple sclerosis (MS) paramagnetic rim lesions (PRLs) are markers of chronic active biology and exhibit complex iron and myelin changes that may complicate quantification when using conventional MRI approaches.

Purpose: To conduct a multiparametric MRI analysis of PRLs.

Study type: Retrospective/longitudinal.

Subjects: Ninety-five progressive MS subjects with at least one persistent PRL who were enrolled in the CONSONANCE trial.

Field strength/sequence: 3-T/Susceptibility-weighted, T1-weighted, T2-weighted, and fluid-attenuated inversion recovery.

Assessment: Acute/chronic PRLs and non-PRLs were measured at screening, 24, 48, and 96 weeks using quantitative magnetic susceptibility (QS), R2*, and standardized T1w/T2w ratio (sT1w/T2w). PRL analyses were performed for whole lesion, core, and rim. The correlations between PRL core and rim sT1w/T2w, QS, and R2* were assessed.

Statistical tests: Linear mixed models. A P-value <0.05 was considered significant.

Results: There was a significant decrease in sT1w/T2w (-0.24 ± -5.3 × 10-3) and R2* (-3.6 ± 2.2 Hz) but a significant increase in QS (+21 ± 1.3 ppb) using whole-lesion analysis of chronic PRLs compared to non-PRLs at screening. Tissue damage accumulated at the 96-week time point was more evident in acute/chronic PRLs compared to acute/chronic non-PRLs (ΔsT1w/T2w = -0.21/-0.24 ± 0.033/0.0053; ΔR2* = -4.4/-3.6 ± 1.4/2.2 Hz). New, acute PRL sT1w/T2w significantly increased in lesion core (+4.3 × 10-3 ± 1.2 × 10-4) and rim (+5.6 × 10-3 ± 1.2 × 10-4) 24 weeks post lesion inception, suggestive of partial recovery. Chronic PRLs, contrastingly, showed significant decreases in sT1w/T2w over the initial 24 weeks for both core (-2.1 × 10-4 ± 2.0 × 10-5) and rim (-2.4 × 10-4 ± 2.0 × 10-5), indicative of irreversible tissue damage. Significant positive correlations between PRL core and rim sT1w/T2w (R2 = 0.53), R2* (R2 = 0.69) and QS (R2 = 0.52) were observed.

Data conclusion: Multiparametric assessment of PRLs has the potential to be a valuable tool for assessing complex iron and myelin changes in chronic active PRLs of progressive MS patients.

Level of evidence: 2 TECHNICAL EFFICACY: Stage 3.

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