Aburashed Rany, Eghzawi Ansam, Long Daniel, Pace Robert, Madha Ali, Cote Jeanie
Insight Hospital and Medical Center, Chicago, IL 60616, USA.
Neurogen Biomarking LLC, Dover, DE 19901, USA.
Neurol Int. 2025 Apr 11;17(4):56. doi: 10.3390/neurolint17040056.
Neurofilament light chain (NfL), an abundant cytoskeletal protein in neurons, has emerged as a promising serum biomarker that indicates non-specific neuronal damage secondary to various neurologic diseases, including multiple sclerosis (MS). Emerging evidence suggests that serum NfL levels correlate with future disability, brain atrophy, predict new disease activity, and decrease in response to various disease-modifying therapies. As research continues to validate NfL's potential role in clinical practice, the need for a practical model to conceptualize and visualize its relevance to MS pathology becomes evident-not only for healthcare providers but also for patients. To address this, we propose the Neurofoundational Model (NFM), which likens a neuron to a home, with various parts of the home representing distinct regions of the central nervous system (CNS). In this model, the home (neuron) experiences scenarios such as a fire, an earthquake, and a slow flood, representing distinct MS disease states. A fire illustrates an MS relapse with good recovery, where serum NfL levels rise during the relapse and subsequently return near baseline. An earthquake represents an MS relapse with poor recovery, where NfL levels increase and remain elevated above baseline. Finally, a slow flood depicts MS in progressive stages, characterized by sustained and gradually increasing serum NfL levels without abrupt clinical changes. This approach offers a clear and relatable visualization for clinicians and patients alike, illustrating the dynamics of serum NfL levels during CNS damage caused by demyelination. By integrating this model into clinical practice, we aim to enhance understanding and communication regarding the role of NfL in MS pathology and its potential utility as a biomarker.
神经丝轻链(NfL)是神经元中一种丰富的细胞骨架蛋白,已成为一种很有前景的血清生物标志物,可指示继发于包括多发性硬化症(MS)在内的各种神经系统疾病的非特异性神经元损伤。越来越多的证据表明,血清NfL水平与未来的残疾、脑萎缩相关,可预测新的疾病活动,并随着各种疾病修正疗法的应用而降低。随着研究不断验证NfL在临床实践中的潜在作用,不仅对于医疗服务提供者,而且对于患者而言,都明显需要一个实用模型来概念化并可视化其与MS病理的相关性。为解决这一问题,我们提出了神经基础模型(NFM),该模型将神经元比作一个家,家中的各个部分代表中枢神经系统(CNS)的不同区域。在这个模型中,家(神经元)经历诸如火灾、地震和缓慢洪水等情景,分别代表不同的MS疾病状态。火灾说明MS复发后恢复良好,复发期间血清NfL水平升高,随后接近基线水平。地震代表MS复发后恢复不佳,NfL水平升高并持续高于基线。最后,缓慢洪水描绘了MS的进展阶段,其特征是血清NfL水平持续且逐渐升高,而无明显的临床变化。这种方法为临床医生和患者提供了清晰且易于理解的可视化,说明了脱髓鞘导致中枢神经系统损伤期间血清NfL水平的动态变化。通过将该模型整合到临床实践中,我们旨在增进对NfL在MS病理中的作用及其作为生物标志物的潜在效用的理解和沟通。