Markers of axonal injury in blood and tissue triggered by acute and chronic demyelination - Scorecard - MDSpire

Markers of axonal injury in blood and tissue triggered by acute and chronic demyelination

  • By

  • Ahmed Abdelhak

  • Christian Cordano

  • Greg J Duncan

  • Katie Emberley

  • Sonia Nocera

  • Wendy Xin

  • Kirtana Ananth

  • Nour Jabassini

  • Kiarra Ning

  • Henriette Reinsberg

  • Frederike Cosima Oertel

  • Alexandra Beaudry-Richard

  • Jens Kuhle

  • Axel Petzold

  • Praveen J Patel

  • Ana P Ribeiro Reis

  • Paul J Foster

  • UKBB Eye and Vision Consortium

  • Trent Watkins

  • Jonah R Chan

  • Ben Emery

  • Ari J Green

  • April 25, 2025

  • 0 min

Share

Clinical Scorecard: Indicators of Axonal Damage in Blood and Tissue Induced by Acute and Chronic Demyelination

At a Glance

CategoryDetail
ConditionDemyelinating diseases including multiple sclerosis
Key MechanismsNeuroaxonal injury driven by demyelination; neurofilament light chain (NfL) release as a biomarker of axonal damage
Target PopulationPeople with multiple sclerosis and animal models of demyelination
Care SettingNeurology clinical and research settings focusing on neurodegenerative and demyelinating disorders

Key Highlights

  • Blood NfL levels correlate robustly with tissue neuroaxonal injury and severity of inflammatory demyelination in experimental autoimmune encephalomyelitis (EAE).
  • Inducible genetic demyelination models show serum NfL peaks during demyelination and decreases following remyelination.
  • In multiple sclerosis patients, NfL levels associate with myelin breakdown proteins, supporting NfL as a translational biomarker for neuroaxonal pathology.

Guideline-Based Recommendations

Diagnosis

  • Use blood NfL measurement as a biomarker to monitor neuroaxonal injury longitudinally in demyelinating diseases.
  • Combine NfL assays with proteomic approaches to assess myelin integrity and neurodegeneration.

Management

  • Consider treatments that promote remyelination to reduce NfL levels and potentially mitigate neuroaxonal injury.
  • Monitor NfL levels to evaluate therapeutic efficacy, including remyelinating agents like clemastine.

Monitoring & Follow-up

  • Regularly measure serum NfL to track disease activity and neuroaxonal damage progression in multiple sclerosis.
  • Use NfL dynamics to assess response to disease-modifying therapies and remyelination interventions.

Risks

  • Elevated NfL indicates ongoing neuroaxonal injury and risk of irreversible disability.
  • Interpret NfL changes considering that structural axonal damage is not the sole cause of elevation; myelin integrity alterations also influence levels.

Patient & Prescribing Data

People with multiple sclerosis undergoing disease-modifying or remyelinating treatments

NfL levels decrease following effective remyelination therapy, suggesting neuroprotection and potential reversibility of axonal pathology.

Clinical Best Practices

  • Incorporate blood NfL assays as part of routine monitoring in demyelinating conditions to detect neuroaxonal injury early.
  • Use animal models of demyelination to understand NfL biology and validate biomarkers before clinical application.
  • Interpret NfL results in the context of both inflammatory activity and myelin integrity changes for comprehensive patient assessment.

References

Original Source(s)

Related Content