A future of AI-driven personalized care for people with multiple sclerosis

Front Immunol. 2024 Aug 19:15:1446748. doi: 10.3389/fimmu.2024.1446748. eCollection 2024.

Abstract

Multiple sclerosis (MS) is a devastating immune-mediated disorder of the central nervous system resulting in progressive disability accumulation. As there is no cure available yet for MS, the primary therapeutic objective is to reduce relapses and to slow down disability progression as early as possible during the disease to maintain and/or improve health-related quality of life. However, optimizing treatment for people with MS (pwMS) is complex and challenging due to the many factors involved and in particular, the high degree of clinical and sub-clinical heterogeneity in disease progression among pwMS. In this paper, we discuss these many different challenges complicating treatment optimization for pwMS as well as how a shift towards a more pro-active, data-driven and personalized medicine approach could potentially improve patient outcomes for pwMS. We describe how the 'Clinical Impact through AI-assisted MS Care' (CLAIMS) project serves as a recent example of how to realize such a shift towards personalized treatment optimization for pwMS through the development of a platform that offers a holistic view of all relevant patient data and biomarkers, and then using this data to enable AI-supported prognostic modelling.

Keywords: AI; data; diagnosis; disease progression; multiple sclerosis; personalized medicine; prognosis.

MeSH terms

  • Artificial Intelligence* / trends
  • Biomarkers
  • Disease Progression
  • Humans
  • Multiple Sclerosis* / immunology
  • Multiple Sclerosis* / therapy
  • Precision Medicine* / methods
  • Precision Medicine* / trends
  • Prognosis
  • Quality of Life

Substances

  • Biomarkers

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The CLAIMS project is supported by the Innovative Health Initiative Joint Undertaking (JU) under grant agreement No 101112153. The JU receives support from the European Union’s Horizon Europe research and innovation program and COCIR, EFPIA, EuropaBio, MedTech Europe, Vaccines Europe, AB Science SA and Icometrix NV. This work was partially supported by an ITEA grant (20030 HeKDisco, HBC.2021.0500) from Flanders Innovation and Entrepreneurship. DH has received support from the Charles University Cooperation Program in Neuroscience, from the National Institute for Neurological Research (Program EXCELES, ID Project No. LX22NPO5107), from the European Union –Next Generation EU, and from the General University Hospital in Prague (project MH CZ-RVO-VFN64165).