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. Author manuscript; available in PMC: 2023 Feb 1.
Published in final edited form as: Mult Scler Relat Disord. 2022 Jan 11;58:103525. doi: 10.1016/j.msard.2022.103525

Table 1:

Comparison of acute optic neuritis from MOG antibody associated disease and multiple sclerosis

MOGAD
N=64 subjects (96 eyes)
Multiple sclerosis
N=50 subjects (51 eyes)
p-value
Age at onset (years), median (IQR) 46.5 (34.3–57) 30.4 (25.7–38.4) <0.001
Female sex, n (%) 39 (61%) 42 (84%) 0.01
Ethnicity, n (%) White, 37 (58%)
African American, 5 (8%)
Asian, 17 (27%)
Hispanic, 4 (6%)
Other/unknown, 1 (2%)
White, 27 (54%)
African American, 16 (32%)
Asian, 2 (4%)
Hispanic, 0 (0%)
Other/unknown, 5 (10%)
<0.001
Affected eye pRNFL, μm, median (IQR) 164 (116–212) 103 (93–113) <0.001
pRNFL thickening1,2, μm, median (IQR) 45.5 (17–105) 7.5 (1–18) <0.001
GCIPL thickness, μm, median (IQR) 79 (76–83.5) 79 (75–84) 0.72

Abbreviations: MOG (myelin oligodendrocyte glycoprotein), pRNFL (peripapillary retinal nerve fiber layer), GCIPL (ganglion cell inner plexiform layer).

1

n=31 MOGAD and 48 MS eyes

2

Estimated using the contralateral unaffected eye as a surrogate for the baseline pRNFL thickness or a baseline optical coherence tomography scan prior to ON onset (if available), n=31 MOGAD and 48 MS subjects/eyes