论文标题

多发性硬化症中的皮质病变,中静脉征兆和顺磁性损伤:新兴的机器学习技术和未来途径

Cortical lesions, central vein sign, and paramagnetic rim lesions in multiple sclerosis: emerging machine learning techniques and future avenues

论文作者

La Rosa, Francesco, Wynen, Maxence, Al-Louzi, Omar, Beck, Erin S, Huelnhagen, Till, Maggi, Pietro, Thiran, Jean-Philippe, Kober, Tobias, Shinohara, Russell T, Sati, Pascal, Reich, Daniel S, Granziera, Cristina, Absinta, Martina, Cuadra, Meritxell Bach

论文摘要

当前的多发性硬化症(MS)诊断标准缺乏特异性,这可能导致误诊,这在当今的临床实践中仍然是一个问题。此外,常规生物标志物仅与MS疾病进展中适度相关。最近,在专用磁共振成像(MRI)序列中可见的高级MS病变成像生物标志物,例如皮质病变(CL),中央静脉(CVS)和顺磁性RIM病变(PRL),在不同诊断中显示出较高的特异性。此外,研究表明,CL和PRL是潜在的预后生物标志物,前者与认知障碍相关,而后者与早期残疾进展相关。由于基于机器学习的方法在评估常规成像生物标志物(例如白质病变细分)方面已经实现了非凡的性能,因此也为CL,CVS和PRL提出了几种自动化或半自动化方法。在本评论中,我们首先介绍了这些高级MS成像生物标志物及其成像方法。随后,我们描述了用于解决这些临床问题的相应基于机器学习的方法,将它们置于他们仍面临的挑战的背景下,包括非标准化的MRI协议,有限的数据集和中等评估者间的变异性。我们通过提出当前的限制来结束,以防止其更广泛的部署并提出未来的研究指示。

The current multiple sclerosis (MS) diagnostic criteria lack specificity, and this may lead to misdiagnosis, which remains an issue in present-day clinical practice. In addition, conventional biomarkers only moderately correlate with MS disease progression. Recently, advanced MS lesional imaging biomarkers such as cortical lesions (CL), the central vein sign (CVS), and paramagnetic rim lesions (PRL), visible in specialized magnetic resonance imaging (MRI) sequences, have shown higher specificity in differential diagnosis. Moreover, studies have shown that CL and PRL are potential prognostic biomarkers, the former correlating with cognitive impairments and the latter with early disability progression. As machine learning-based methods have achieved extraordinary performance in the assessment of conventional imaging biomarkers, such as white matter lesion segmentation, several automated or semi-automated methods have been proposed for CL, CVS, and PRL as well. In the present review, we first introduce these advanced MS imaging biomarkers and their imaging methods. Subsequently, we describe the corresponding machine learning-based methods that were used to tackle these clinical questions, putting them into context with respect to the challenges they are still facing, including non-standardized MRI protocols, limited datasets, and moderate inter-rater variability. We conclude by presenting the current limitations that prevent their broader deployment and suggesting future research directions.

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