AI-driven reclassification of multiple sclerosis progression

IF 50 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Habib Ganjgahi, Dieter A. Häring, Piet Aarden, Gordon Graham, Yang Sun, Stephen Gardiner, Wendy Su, Claude Berge, Antje Bischof, Elizabeth Fisher, Laura Gaetano, Stefan P. Thoma, Bernd C. Kieseier, Thomas E. Nichols, Alan J. Thompson, Xavier Montalban, Fred D. Lublin, Ludwig Kappos, Douglas L. Arnold, Robert A. Bermel, Heinz Wiendl, Chris C. Holmes
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Abstract

Multiple sclerosis (MS) affects 2.9 million people. Traditional classification of MS into distinct subtypes poorly reflects its pathobiology and has limited value for prognosticating disease evolution and treatment response, thereby hampering drug discovery. Here we report a data-driven classification of MS disease evolution by analyzing a large clinical trial database (approximately 8,000 patients, 118,000 patient visits and more than 35,000 magnetic resonance imaging scans) using probabilistic machine learning. Four dimensions define MS disease states: physical disability, brain damage, relapse and subclinical disease activity. Early/mild/evolving (EME) MS and advanced MS represent two poles of a disease severity spectrum. Patients with EME MS show limited clinical impairment and minor brain damage. Transitions to advanced MS occur via brain damage accumulation through inflammatory states, with or without accompanying symptoms. Advanced MS is characterized by moderate to high disability levels, radiological disease burden and risk of disease progression independent of relapses, with little probability of returning to earlier MS states. We validated these results in an independent clinical trial database and a real-world cohort, totaling more than 4,000 patients with MS. Our findings support viewing MS as a disease continuum. We propose a streamlined disease classification to offer a unifying understanding of the disease, improve patient management and enhance drug discovery efficiency and precision.

Abstract Image

人工智能驱动的多发性硬化症进展再分类
多发性硬化症(MS)影响着290万人。传统的MS亚型分类不能很好地反映MS的病理生物学特性,对疾病发展和治疗反应的预测价值有限,从而阻碍了药物的发现。在这里,我们通过使用概率机器学习分析大型临床试验数据库(约8,000名患者,118,000名患者就诊和超过35,000次磁共振成像扫描),报告了MS疾病演变的数据驱动分类。四个维度定义MS疾病状态:身体残疾、脑损伤、复发和亚临床疾病活动。早期/轻度/发展(EME) MS和晚期MS代表疾病严重程度谱的两极。EME MS患者表现出有限的临床损害和轻微的脑损伤。通过炎症状态的脑损伤积累,伴有或不伴有症状,过渡到晚期多发性硬化症。晚期多发性硬化症的特点是中度至高度残疾水平、放射学疾病负担和独立于复发的疾病进展风险,几乎不可能恢复到早期多发性硬化症状态。我们在一个独立的临床试验数据库和一个真实世界的队列中验证了这些结果,总共有4000多名MS患者。我们的发现支持将MS视为一种疾病连续体。我们提出了一种简化的疾病分类,以提供对疾病的统一认识,改善患者管理,提高药物发现的效率和准确性。
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来源期刊
Nature Medicine
Nature Medicine 医学-生化与分子生物学
CiteScore
100.90
自引率
0.70%
发文量
525
审稿时长
1 months
期刊介绍: Nature Medicine is a monthly journal publishing original peer-reviewed research in all areas of medicine. The publication focuses on originality, timeliness, interdisciplinary interest, and the impact on improving human health. In addition to research articles, Nature Medicine also publishes commissioned content such as News, Reviews, and Perspectives. This content aims to provide context for the latest advances in translational and clinical research, reaching a wide audience of M.D. and Ph.D. readers. All editorial decisions for the journal are made by a team of full-time professional editors. Nature Medicine consider all types of clinical research, including: -Case-reports and small case series -Clinical trials, whether phase 1, 2, 3 or 4 -Observational studies -Meta-analyses -Biomarker studies -Public and global health studies Nature Medicine is also committed to facilitating communication between translational and clinical researchers. As such, we consider “hybrid” studies with preclinical and translational findings reported alongside data from clinical studies.
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