Neurology· Topic 10.11 Multiple sclerosis and neuro-ophthalmic disorders· 10.11.1

Multiple sclerosis

Multiple sclerosis is an autoimmune, demyelinating CNS disorder causing optic neuritis, myelitis, and brainstem/cerebellar syndromes separated in space and time. Diagnosis uses the McDonald MRI-based criteria; acute relapses are treated with high-dose glucocorticoids, and disease-modifying therapy (interferon beta, glatiramer, or a higher-efficacy agent such as ocrelizumab or natalizumab) is started early to prevent relapse and disability accumulation.

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What this article covers

  • Overview

    Autoimmune demyelinating CNS disorder: multiple sclerosis (MS) causes inflammatory damage to the brain, spinal cord, and optic nerve, with most overt clinical symptoms resulting directly from…

  • Epidemiology

    Female predominance: female-to-male ratio is about 2:1.

  • Risk factors

    Genetic susceptibility: MS is associated with the HLA-DRB1 locus, with higher risk given a family history of autoimmune disease.

  • Pathophysiology

    Immune-mediated demyelination: MS is an autoimmune disorder in which inflammatory attack on CNS myelin interrupts axonal conduction, producing the clinical relapse; relapses evolve over hours to days and typically peak over days to weeks.

  • Clinical features

    Optic neuritis: subacute unilateral visual loss, sometimes with pain on eye movement or flashing lights (photopsia); examination shows reduced acuity, a scotoma or visual field deficit, impaired…

  • Differential diagnosis

    Neuromyelitis optica spectrum disorder: longitudinally extensive spinal cord lesions (=3 vertebral segments) and severe, often bilateral optic neuritis with aquaporin-4 antibody positivity, unlike…

  • Diagnosis

    The McDonald criteria establish the diagnosis by requiring symptoms of CNS demyelination separated in space and time, demonstrated through a combination of clinical relapses or progression…

  • Management

    First, confirm a true relapse (new or worsening neurologic symptoms lasting more than 24 hours) and exclude a pseudorelapse by evaluating for infection or another Uhthoff trigger before starting treatment.

  • Complications

    Secondary progressive MS: gradual disability accumulation independent of relapses, though disease-modifying therapy has reduced conversion rates.

  • Prognosis

    Course varies widely: relapsing-remitting MS carries the most favorable prognosis, while primary and secondary progressive forms carry a higher burden of accumulating disability.

  • Prevention

    No primary prevention exists once genetic and environmental risk (latitude, EBV exposure) has occurred, so efforts focus on relapse and disability prevention after diagnosis.

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