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A dual modeling approach to automatic segmentation of cerebral T2 hyperintensities and T1 black holes in multiple sclerosis

机译:自动分割多发性硬化症中脑T2高信号和T1黑洞的双重建模方法

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Background and purposeMagnetic resonance imaging (MRI) is crucial for in vivo detection and characterization of white matter lesions (WML) in multiple sclerosis (MS). The most widely established MRI outcome measure is the volume of hyperintense lesions on T2-weighted images (T2L). Unfortunately, T2L are non-specific for the level of tissue destruction and show a weak relationship to clinical status. Interest in lesions that appear hypointense on T1-weighted images (T1L) (“black holes”) has grown because T1L provide more specificity for axonal loss and a closer link to neurologic disability. The technical difficulty of T1L segmentation has led investigators to rely on time-consuming manual assessments prone to inter- and intra-rater variability. This study aims to develop an automatic T1L segmentation approach, adapted from a T2L segmentation algorithm.Materials and methodsT1, T2, and fluid-attenuated inversion recovery (FLAIR) sequences were acquired from 40 MS subjects at 3 Tesla (3?T). T2L and T1L were manually segmented. A Method for Inter-Modal Segmentation Analysis (MIMoSA) was then employed.ResultsUsing cross-validation, MIMoSA proved to be robust for segmenting both T2L and T1L. For T2L, a S?rensen-Dice coefficient (DSC) of 0.66 and partial AUC (pAUC) up to 1% false positive rate of 0.70 were achieved. For T1L, 0.53 DSC and 0.64 pAUC were achieved. Manual and MIMoSA segmented volumes were correlated and resulted in 0.88 for T1L and 0.95 for T2L. The correlation between Expanded Disability Status Scale (EDSS) scores and manual versus automatic volumes were similar for T1L (0.32 manual vs. 0.34 MIMoSA), T2L (0.33 vs. 0.32), and the T1L/T2L ratio (0.33 vs 0.33).ConclusionsThough originally designed to segment T2L, MIMoSA performs well for segmenting T1 black holes in patients with MS.
机译:背景与目的磁共振成像(MRI)对于多发性硬化症(MS)中白质病变(WML)的体内检测和表征至关重要。建立最广泛的MRI结果指标是T2加权图像(T2L)上的高强度病变的体积。不幸的是,T2L对组织破坏的水平不是特异性的,并且与临床状态之间的关系较弱。人们对在T1加权图像(T1L)(“黑洞”)上出现低断点的病变的兴趣日益浓厚,因为T1L为轴突缺失提供了更多的特异性,并与神经功能障碍密切相关。 T1L细分的技术难度使研究人员不得不依赖费时的人工评估,而这种评估容易造成评分者之间和评分者内部的差异。本研究旨在开发一种适用于T2L分割算法的自动T1L分割方法,从3位特斯拉(3?T)的40名MS受试者中获取了材料和方法T1,T2和流体衰减反转恢复(FLAIR)序列。手动分割了T2L和T1L。结果,通过交叉验证,MIMoSA被证明对分割T2L和T1L都是鲁棒的。对于T2L,S?rensen-Dice系数(DSC)为0.66,部分AUC(pAUC)的误报率高达1%,为0.70。对于T1L,获得了0.53 DSC和0.64 pAUC。手动和MIMoSA分割的体积相互关联,得出T1L为0.88,T2L为0.95。 T1L(0.32手动对比0.34 MIMoSA),T2L(0.33对比0.32)和T1L / T2L比(0.33对比0.33)的扩展残疾状态量表(EDSS)评分与手动与自动量之间的相关性相似。 MIMoSA最初设计用于分割T2L,可很好地分割MS患者的T1黑洞。

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