Abstract

We aimed to investigate the frequency of asymptomatic acute brain MRI abnormalities accompanying optic neuritis (ON) or myelitis in neuromyelitis optica spectrum disorder (NMOSD) patients with aquaporin-4 antibodies (AQP4-Ab). We reviewed 324 brain MRI scans that were obtained during acute attacks of ON or myelitis, in 165 NMOSD patients with AQP4-Ab. We observed that acute asymptomatic NMOSD-typical brain lesions accompanied 27 (8%) acute attacks of ON or myelitis in 24 (15%) patients. The most common asymptomatic brain abnormalities included edematous corpus callosum lesions (n = 17), followed by lesions on the internal capsule and/or cerebral peduncle lesions (n = 9), periependymal surfaces of the fourth ventricle (n = 5), large deep white matter lesions (n = 4), periependymal cerebral lesions surrounding the lateral ventricles (n = 3), and hypothalamic lesions (n = 1). If asymptomatic NMOSD-typical brain abnormalities were considered as evidence for DIS, while also assuming that the AQP4-IgG status was unknown, the median time to diagnosis using the 2015 diagnosis criteria for NMOSD was shortened from 28 months to 6 months (p = 0.008). Asymptomatic acute NMOSD-typical brain lesions can be accompanied by an acute attack of ON or myelitis. Identifying these asymptomatic brain lesions may help facilitate earlier diagnosis of NMOSD.

Highlights

  • Brain magnetic resonance imaging (MRI) abnormalities are frequently observed in patients with neuromyelitis optica spectrum disorder (NMOSD) [1,2,3,4,5,6], and some characteristic MRI abnormalities are incorporated into the recently proposed diagnostic criteria for NMOSD [7]

  • We identified a total of 1554 attacks in 222 NMOSD patients over a median disease duration of 9 years

  • Most asymptomatic brain lesions occurred before immunosuppressive therapy and asymptomatic brain lesions were found after immunosuppressive treatment in 6 MRIs taken from 5 patients

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Summary

Introduction

Brain magnetic resonance imaging (MRI) abnormalities are frequently observed in patients with neuromyelitis optica spectrum disorder (NMOSD) [1,2,3,4,5,6], and some characteristic MRI abnormalities are incorporated into the recently proposed diagnostic criteria for NMOSD [7]. We previously examined the clinical characteristics of 106 seropositive NMOSD patients, and found that brain MRI abnormalities (72%) were more frequent than clinical brain symptoms (51%) [8]. He serves on a steering committee for MedImmune and as a coeditor for Multiple Sclerosis Journal – Experimental, Translational and Clinical. This does not alter our adherence to all the PLOS one policies on sharing data and materials, as detailed online in the guide for authors

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