Dynamic Expansion and Contraction of Multiple Sclerosis T2-weighted Hyperintense Lesions are Present Below the Threshold of Visual Perception.

Darin T Okuda, Tatum M Moog, Morgan McCreary, Kevin Shan, Kasia Zubkow, Braeden D Newton, Alexander D Smith, Mahi A Patel, Katy W Burgess, Christine Lebrun-Frénay
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Abstract

Background and purpose: The study of T2-weighted hyperintense lesions resulting from autoimmune inflammatory injury and associated volumes within the CNS remains fundamental to the diagnosis and disease surveillance of multiple sclerosis (MS). We investigated the dynamic changes of individual T2-weighted hyperintense MS lesions on MRI and hypothesized that variations may be present below the threshold of visual perception when evaluating longitudinal data.

Materials and methods: A retrospective study was performed of people with MS, incorporating data from three consecutive MRI time points acquired within a single academic center. All included MRI studies lacked formal imaging interpretations of newly enlarging or contracting T2-weighted hyperintensities. Well defined, non-coalescing, individual T2-weighted hyperintense lesions were targeted. A total of 8-12 lesions were randomly selected in a blinded fashion at MRI time point 1 and 3-dimensional lesion volumes followed over MRI time points 2 and 3. The impact of treatment on lesion expansion and relationship to brain MRI advancement, patient-reported progression of disease, and physician-identified progression was also studied.

Results: The study cohort was comprised of 115 people (81 (70.4%) female; mean disease duration of 6.62 years(y) (standard deviation: 6.68y)) who were primarily White (79.1%). A total of 1,426 focal T2-weighted hyperintense MS lesions were identified on MRI time point 1 and longitudinally followed over MRI time points 2 and 3. In the evaluation of raw changes in individual T2-weighted hyperintense lesion volumes from MRI time point 1 to MRI time point 2, a similar number of individuals were observed with predominantly expanding (49/115; 42.6%) or contracting (51/115; 44.3%) lesions. However, the majority of lesions expanded in volume (48/115; 41.7%) versus those that contracted (45/115; 39.1%) when evaluating MRI time point 3 to time point 1. Those individuals not on active treatment had a 67.15% reduction in the odds of more individual lesions predominantly contracting in volume relative to those on low-efficacy disease modifying therapy treatment (95% CI=[-83.89, -33.01], p=0.0008) and 74.02% reduction for those on high-efficacy treatment (95% CI=[-87.37%,-46.56%], p<0.0001).

Conclusions: Dynamic changes in T2-weighted hyperintense lesions are abundant, occurring below the threshold of visual perception and are present more frequently in untreated individuals.

Abbreviations: MS = multiple sclerosis; DMT = disease modifying therapy; 2D = 2-dimensional; 3D = 3-dimensional; LMS = Lambda, Mu, and Sigma.

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多发性硬化症 T2 加权高强度病变的动态扩展和收缩存在于视觉感知阈值以下。
背景和目的:研究中枢神经系统内自身免疫性炎症损伤导致的T2加权高密度病变及相关体积仍然是多发性硬化症(MS)诊断和疾病监测的基础。我们研究了核磁共振成像上单个 T2 加权高密度 MS 病灶的动态变化,并假设在评估纵向数据时,变化可能存在于视觉感知阈值以下:对多发性硬化症患者进行了一项回顾性研究,纳入了在一个学术中心获得的三个连续 MRI 时间点的数据。所有纳入的磁共振成像研究均缺乏对新增大或收缩的 T2 加权高密度的正式成像解释。研究对象为定义明确、不凝聚的单个 T2 加权高密度病灶。在磁共振成像时间点 1 以盲法随机抽取 8-12 个病灶,并在磁共振成像时间点 2 和 3 跟踪三维病灶体积。此外,还研究了治疗对病灶扩大的影响以及与脑部 MRI 进展、患者报告的疾病进展和医生认定的疾病进展之间的关系:研究队列由 115 人组成(81 人(70.4%)为女性;平均病程为 6.62 年(标准差:6.68 年)),主要为白人(79.1%)。在核磁共振成像时间点 1 上共确定了 1,426 个 T2 加权高强度多发性硬化病灶,并在核磁共振成像时间点 2 和 3 上进行了纵向跟踪。在评估从核磁共振成像时间点 1 到核磁共振成像时间点 2 单个 T2 加权高密度病灶体积的原始变化时,观察到相似数量的患者病灶主要在扩大(49/115;42.6%)或缩小(51/115;44.3%)。然而,在评估核磁共振成像时间点 3 与时间点 1 时,大多数病变的体积扩大(48/115;41.7%),而病变的体积缩小(45/115;39.1%)。与接受低效疾病调整疗法治疗的患者相比,未接受积极治疗的患者出现更多单个病灶体积收缩的几率降低了67.15%(95% CI=[-83.89,-33.01],P=0.0008),而接受高效治疗的患者出现单个病灶体积收缩的几率降低了74.02%(95% CI=[-87.37%,-46.56%],P结论:T2加权高张力病变的动态变化非常丰富,发生在视觉感知阈值以下,在未经治疗的患者中更常出现:缩写:MS = 多发性硬化;DMT = 疾病调整疗法;2D = 二维;3D = 三维;LMS = Lambda、Mu 和 Sigma。
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