Mina M. Huerta, Devon S. Conway, Sarah M. Planchon, Bhaskar Thoomukuntla, Oh Se-Hong, Ken E. Sakaie, Daniel Ontaneda, Kunio Nakamura
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Magnetom 7T scanner was used to acquire magnetization-prepared 2 rapid acquisition gradient echo and advanced MRI including visualization of short transverse relaxation time component (ViSTa) for myelin, quantitative magnetization transfer (qMT) for myelin, and neurite orientation dispersion density imaging (NODDI). SELs were defined as lesions showing ≥12% of growth over 12 months on serial MRI. Comparisons of quantitative measures in SELs and non-SELs were performed at baseline and over time. Statistical analyses included two-sample <i>t</i>-test, analysis of variance, and mixed-effects linear model for MRI metrics between lesion types.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A total of 1075 lesions were evaluated. Two hundred twenty-four lesions (21%) were SELs, and 216 (96%) of the SELs were black holes. At baseline, compared to non-SELs, SELs showed significantly lower ViSTa (1.38 vs. 1.53, <i>p</i> < .001) and qMT (2.47 vs. 2.97, <i>p</i> < .001) but not in NODDI measures (<i>p</i> > .27). Longitudinally, only ViSTa showed a greater loss when comparing SEL and non-SEL (<i>p</i> = .03).</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>SELs have a lower myelin content relative to non-SELs without a difference in neurite measures. 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引用次数: 0
摘要
背景和目的:缓慢扩展病变(SELs)被认为是慢性活动性病变的一个子集,与临床残疾、严重程度和疾病进展有关。本研究的目的是利用先进的磁共振成像(MRI)技术,通过7特斯拉(T)磁共振成像检查与髓鞘和神经元密度相关的指标来描述SEL的特征:研究设计为多发性硬化症患者(n = 15)的回顾性纵向观察队列。使用 Magnetom 7 T 扫描仪采集磁化准备 2 快速采集梯度回波和高级 MRI,包括髓鞘短横向弛豫时间分量可视化(ViSTa)、髓鞘定量磁化转移(qMT)和神经元定向弥散密度成像(NODDI)。SEL的定义是在连续核磁共振成像上显示12个月内增长≥12%的病变。对SEL和非SEL的定量指标进行基线和随时间变化的比较。统计分析包括双样本 t 检验、方差分析和病变类型间 MRI 指标的混合效应线性模型:共评估了 1075 个病灶。其中 224 个病灶(21%)为 SEL,216 个病灶(96%)为黑洞。基线时,与非 SEL 相比,SEL 的 ViSTa 明显较低(1.38 对 1.53,P.27)。纵向比较,SEL 与非 SEL 相比,只有 ViSTa 的损失更大(p = .03):结论:SEL 相对于非 SEL 的髓鞘含量较低,但神经元测量结果没有差异。SEL的表观髓鞘水分率呈纵向下降趋势,反映出组织损伤更严重。
Longitudinal myelin content measures of slowly expanding lesions using 7T MRI in multiple sclerosis
Background and Purpose
Slowly expanding lesions (SELs) are thought to represent a subset of chronic active lesions and have been associated with clinical disability, severity, and disease progression. The purpose of this study was to characterize SELs using advanced magnetic resonance imaging (MRI) measures related to myelin and neurite density on 7 Tesla (T) MRI.
Methods
The study design was retrospective, longitudinal, observational cohort with multiple sclerosis (n = 15). Magnetom 7T scanner was used to acquire magnetization-prepared 2 rapid acquisition gradient echo and advanced MRI including visualization of short transverse relaxation time component (ViSTa) for myelin, quantitative magnetization transfer (qMT) for myelin, and neurite orientation dispersion density imaging (NODDI). SELs were defined as lesions showing ≥12% of growth over 12 months on serial MRI. Comparisons of quantitative measures in SELs and non-SELs were performed at baseline and over time. Statistical analyses included two-sample t-test, analysis of variance, and mixed-effects linear model for MRI metrics between lesion types.
Results
A total of 1075 lesions were evaluated. Two hundred twenty-four lesions (21%) were SELs, and 216 (96%) of the SELs were black holes. At baseline, compared to non-SELs, SELs showed significantly lower ViSTa (1.38 vs. 1.53, p < .001) and qMT (2.47 vs. 2.97, p < .001) but not in NODDI measures (p > .27). Longitudinally, only ViSTa showed a greater loss when comparing SEL and non-SEL (p = .03).
Conclusions
SELs have a lower myelin content relative to non-SELs without a difference in neurite measures. SELs showed a longitudinal decrease in apparent myelin water fraction reflecting greater tissue injury.
期刊介绍:
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