Okuda Darin T, Lebrun-Frénay Christine
Department of Neurology, Neuroinnovation Program, Multiple Sclerosis & Neuroimmunology Imaging Program, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
Peter O'Donnell Jr. Brain Institute, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
J Cent Nerv Syst Dis. 2025 Jan 5;17:11795735241310138. doi: 10.1177/11795735241310138. eCollection 2025.
Multiple sclerosis (MS) falls within the spectrum of central nervous system (CNS) demyelinating diseases that may lead to permanent neurological disability. Fundamental to the diagnosis and clinical surveillance is magnetic resonance imaging (MRI) that allows for the identification of T2-hyperintensities associated with autoimmune injury that demonstrate distinct spatial distribution patterns. Here, we describe the clinical experience of a 31-year-old, right-handed, White man seen in consultation at The University of Texas Southwestern Medical Center in Dallas, Texas, following complaints of headaches that began after head trauma related to military service. Imaging data spanning over 10 years are provided. All MRI data are currently presented in black and white with grayscale values within voxels associated with a single variable, intensity. We transformed these grayscale values into color using generative artificial intelligence (AI). As color allows for the inclusion of three variables: hue, lightness (intensity), and saturation, we hypothesized that additional details may be learned beyond those currently provided with the existing conventional approach of grayscale interpretation. We identified differences in lesion colors that remained consistent from the two MRI timepoints studied. In addition, quantitative R1, R2, and proton density voxel values appeared consistent with the color scheme generated by the AI system. With advancing AI methods and capabilities along with the additional data that color provides in comparison to grayscale, new insights into the biology of disease may be possible. Modifying what we measure in people with chronic conditions and how we present the data may be of greater value than conventional approaches typically used in the study, education, and care of people with MS and other neurological conditions.
多发性硬化症(MS)属于中枢神经系统(CNS)脱髓鞘疾病范畴,可能导致永久性神经功能残疾。诊断和临床监测的基础是磁共振成像(MRI),它能够识别与自身免疫损伤相关的T2高信号,这些高信号呈现出独特的空间分布模式。在此,我们描述了一名31岁、右利手、白人男性的临床经历,该患者因与军事服役相关的头部外伤后出现头痛症状,前来德克萨斯大学西南医学中心(位于德克萨斯州达拉斯)就诊。我们提供了超过10年的成像数据。所有MRI数据目前均以黑白形式呈现,体素内的灰度值与单一变量强度相关。我们使用生成式人工智能(AI)将这些灰度值转换为颜色。由于颜色包含三个变量:色调、亮度(强度)和饱和度,我们推测,与现有的传统灰度解读方法相比,可能会从中了解到更多额外细节。我们在研究的两个MRI时间点上发现病变颜色的差异保持一致。此外,定量的R1、R2和质子密度体素值似乎与AI系统生成的配色方案一致。随着AI方法和能力的不断进步,以及与灰度相比颜色所提供的额外数据,可能会对疾病生物学有新的认识。改变我们在慢性病患者中测量的内容以及数据呈现方式,可能比通常用于MS和其他神经疾病患者研究、教育及护理的传统方法更有价值。