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The changing landscape of optic neuritis: a narrative review

期刊

JOURNAL OF NEUROLOGY
卷 269, 期 1, 页码 111-124

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00415-020-10352-1

关键词

Optic neuritis; Multiple sclerosis; Demyelinating diseases; Optic nerve diseases

资金

  1. National Institutes of Health, Bethesda, MD [K23EY027849]

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Optic neuritis is an inflammatory optic neuropathy that is often associated with demyelinating disorders of the central nervous system. However, it is frequently misdiagnosed in clinical practice, leading to inappropriate treatment or delays in diagnosis. With an increased understanding of immunopathology, novel disease management strategies are emerging to minimize vision loss and improve long-term surveillance.
Optic neuritis (ON) is an inflammatory optic neuropathy that is often a harbinger of central nervous system (CNS) demyelinating disorders. ON is frequently misdiagnosed in the clinical arena, leading to either inappropriate management or diagnostic delays. As a result, patients may fail to achieve optimal recovery. The treatment response to corticosteroids and long term risk of multiple sclerosis was established in the first clinical trials conducted roughly 30 years ago. Spontaneous resolution was observed in the vast majority of patients and intravenous high-dose corticosteroids hastened recovery; half of the patients eventually developed multiple sclerosis. Over the ensuing decades, the number of inflammatory conditions associated with ON has significantly expanded exposing substantial variability in the prognosis, treatment, and management of ON patients. ON subtypes can frequently be distinguished by distinct clinical, serological, and radiological profiles allowing expedited and specialized treatment. Guided by an increased understanding of the immunopathology underlying optic nerve and associated CNS injuries, novel disease management strategies are emerging to minimize vision loss, improve long-term surveillance strategies, and minimize CNS injury and disability. Knowledge regarding the clinical signs and symptoms of different ON subtypes is essential to guide acute therapy, prognosticate recovery, accurately identify underlying CNS inflammatory disorders, and facilitate study design for the next generation of clinical and translational trials.

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