Chiasmatic lesions on conventional magnetic resonance imaging during the first event of optic neuritis in patients with neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein‐associated disease in a Latin American cohort

医学 视神经炎 髓鞘少突胶质细胞糖蛋白 视神经脊髓炎 多发性硬化 磁共振成像 光谱紊乱 放射科 病理 精神科 实验性自身免疫性脑脊髓炎
作者
Edgar Carnero Contentti,Pablo A. López,Juan Criniti,Juan Pablo Pettinicchi,Edgardo Cristiano,Liliana Patrucco,Elisa Bribiesca Contreras,Enrique Gómez‐Figueroa,José Flores-Rivera,Edgar Patricio Correa-Díaz,Ana María Toral Granda,Maria Yepez,Wilson Alfredo Gualotuña Pachacama,Jefferson Santiago Piedra Andrade,Lorna Galleguillos,Verónica Tkachuk,Débora Nadur,Vanessa Daccach Marques,Ibis Soto de Castillo,Magdalena Casas,Leila Cohen,Ricardo Alonso,Alejandro Caride,Marco Aurélio Lana–Peixoto,Juan Ignacio Rojas
出处
期刊:European Journal of Neurology [Wiley]
卷期号:29 (3): 802-809 被引量:4
标识
DOI:10.1111/ene.15178
摘要

Optic neuritis (ON) is often the initial symptom of neuromyelitis optica spectrum disorder (NMOSD) and myelin oligodendrocyte glycoprotein-associated disease (MOGAD). We aimed to compare the frequency and pattern of chiasmatic lesions in MOGAD-related ON (MOGAD-ON) and NMOSD-related ON (NMOSD-ON) using conventional brain imaging (magnetic resonance imaging [MRI]) in Latin America (LATAM).We reviewed the medical records and brain MRI (≤30 days from ON onset) of patients with a first event of MOGAD-ON and NMOSD-ON. Patients from Argentina (n = 72), Chile (n = 21), Ecuador (n = 31), Brazil (n = 30), Venezuela (n = 10) and Mexico (n = 82) were included. Antibody status was tested using a cell-based assay. Demographic, clinical, imaging and prognostic (as measured by the Visual Functional System Score [VFSS] of the Expanded Disability Status Scale) data were compared.A total of 246 patients (208 NMOSD and 38 MOGAD) were included. No differences were found in gender and ethnicity between the groups. We observed chiasmatic lesions in 66/208 (31.7%) NMOSD-ON and in 5/38 (13.1%) MOGAD-ON patients (p = 0.01). Of these patients with chiasmatic lesions, 54/66 (81.8%) and 4/5 had associated longitudinally extensive optic nerve lesions, 45/66 (68%) and 4/5 had bilateral lesions, and 31/66 (47%) and 4/5 showed gadolinium-enhancing chiasmatic lesions, respectively. A positive correlation was observed between VFSS and presence of bilateral (r = 0,28, p < 0.0001), chiasmatic (r = 0.27, p = 0.0001) and longitudinally extensive lesions (r = 0,25, p = 0.0009) in the NMOSD-ON group, but no correlations were observed in the MOGAD-ON group.Chiasmatic lesions were significantly more common in NMOSD than in MOGAD during an ON attack in this LATAM cohort. Further studies are needed to assess the generalizability of these results.
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