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Updated: Aug 20, 2025

Measuring Progressive Neurological Disability in a Mouse Model of Multiple Sclerosis
08:11

Measuring Progressive Neurological Disability in a Mouse Model of Multiple Sclerosis

Published on: November 14, 2016

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Multiple sclerosis progression: time for a new mechanism-driven framework.

Tanja Kuhlmann1, Marcello Moccia2, Timothy Coetzee3

  • 1Institute of Neuropathology, University Hospital Münster, Münster, Germany; Neuroimmunology Unit, Montreal Neurological Institute, McGill University, Montreal, QC, Canada.

The Lancet. Neurology
|November 21, 2022
PubMed
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This summary is machine-generated.

Multiple sclerosis progression is better viewed as a continuum, not distinct stages. Understanding this spectrum of pathological and compensatory processes can improve patient care and treatment targets.

Area of Science:

  • Neurology
  • Neuroimmunology
  • Pathophysiology

Background:

  • Multiple sclerosis (MS) traditionally classified by clinical subtypes: relapsing-remitting (RRMS), secondary progressive (SPMS), and primary progressive (PPMS).
  • These classifications guide patient care, research, and drug approvals.
  • Emerging evidence suggests MS is a continuum rather than discrete stages.

Purpose of the Study:

  • To propose a new conceptualization of multiple sclerosis course as a spectrum.
  • To highlight the role of overlapping pathophysiological and compensatory processes in MS progression.
  • To emphasize the impact of aging on neural injury and resilience in MS.

Main Methods:

  • Review of accumulating evidence on MS pathophysiology.
  • Analysis of the shift from acute injury to widespread inflammation and neurodegeneration.

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  • Consideration of compensatory mechanisms like neuroplasticity and remyelination.
  • Main Results:

    • The clinical course of MS reflects a continuum influenced by varying pathological and compensatory processes.
    • Progression involves a shift from localized injury to widespread inflammation, neurodegeneration, and impaired compensatory mechanisms.
    • Aging exacerbates neural susceptibility and reduces resilience in MS patients.

    Conclusions:

    • Reconsidering MS as a spectrum defined by the interplay of pathological and reparative processes is encouraged.
    • New insights into progression mechanisms and quantification hold promise for clinical care and treatment strategies.
    • This paradigm shift may inform future therapeutic targets and regulatory decision-making for MS treatments.