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Clinical outcomes and prognostic factors in patients with optic neuritis related to NMOSD and MOGAD in distinct ethnic groups from Latin America.
Carnero Contentti, Edgar; López, Pablo A; Criniti, Juan; Pettinicchi, Juan Pablo; Cristiano, Edgardo; Patrucco, Liliana; Bribiesca Contreras, Elisa; Gómez-Figueroa, Enrique; Flores-Rivera, José; Correa-Díaz, Edgar Patricio; Toral Granda, Ana María; Ortiz Yepez, María Angelica; Gualotuña Pachacama, Wilson Alfredo; Piedra Andrade, Jefferson Santiago; Galleguillos, Lorna; Tkachuk, Verónica; Nadur, Débora; Daccach Marques, Vanessa; Soto de Castillo, Ibis; Casas, Magdalena; Cohen, Leila; Alonso, Ricardo; Caride, Alejandro; Lana-Peixoto, Marco; Rojas, Juan Ignacio.
Affiliation
  • Carnero Contentti E; Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina. Electronic address: ecarnerocontentti@hospitalaleman.com.
  • López PA; Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina.
  • Criniti J; Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina.
  • Pettinicchi JP; Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina.
  • Cristiano E; Centro de Esclerosis Múltiple de Buenos Aires (CEMBA), Buenos Aires, Argentina.
  • Patrucco L; Centro de Esclerosis Múltiple de Buenos Aires (CEMBA), Buenos Aires, Argentina.
  • Bribiesca Contreras E; Division of Neurology, National Institute of Neurology and Neurosurgery, Mexico City, Mexico.
  • Gómez-Figueroa E; Division of Neurology, National Institute of Neurology and Neurosurgery, Mexico City, Mexico.
  • Flores-Rivera J; Division of Neurology, National Institute of Neurology and Neurosurgery, Mexico City, Mexico.
  • Correa-Díaz EP; Neurology Department, Hospital Carlos Andrade Marin, Universidad Central del Ecuador, Quito, Ecuador.
  • Toral Granda AM; Neurology Department, Hospital José Carrasco Arteaga de Cuenca, Ecuador.
  • Ortiz Yepez MA; Neurology Department, Hospital Carlos Andrade Marin, Universidad Central del Ecuador, Quito, Ecuador.
  • Gualotuña Pachacama WA; Neurology Department, Hospital Carlos Andrade Marin, Universidad Central del Ecuador, Quito, Ecuador.
  • Piedra Andrade JS; Neurology Department, Hospital Carlos Andrade Marin, Universidad Central del Ecuador, Quito, Ecuador.
  • Galleguillos L; Clínica Alemana de Santiago, Santiago, Chile.
  • Tkachuk V; Neuroimmunology Section, Department of Neurology, Hospital de Clínicas "José de San Martín", Buenos Aires, Argentina.
  • Nadur D; Neuroimmunology Section, Department of Neurology, Hospital de Clínicas "José de San Martín", Buenos Aires, Argentina.
  • Daccach Marques V; Department of Neurosciences and Behavioral Sciences, Hospital das Clínicas, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil.
  • Soto de Castillo I; Neurology Department, Hospital Universitario de Maracaibo, Maracaibo, Bolivarian Republic of Venezuela.
  • Casas M; Neurology Department, Hospital J.M. Ramos Mejía, Faculty of Medicine, University of Buenos Aires, Buenos Aires, Argentina.
  • Cohen L; Neurology Department, Hospital J.M. Ramos Mejía, Faculty of Medicine, University of Buenos Aires, Buenos Aires, Argentina.
  • Alonso R; Neurology Department, Hospital J.M. Ramos Mejía, Faculty of Medicine, University of Buenos Aires, Buenos Aires, Argentina.
  • Caride A; Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina.
  • Lana-Peixoto M; Department of Neurology, Federal University of Minas Gerais Medical School, Belo Horizonte, Brazil.
  • Rojas JI; Centro de Esclerosis Múltiple de Buenos Aires (CEMBA), Buenos Aires, Argentina; Service of Neurology, Hospital Universitario de CEMIC, Buenos Aires, Argentina.
Mult Scler Relat Disord ; 72: 104611, 2023 Apr.
Article in En | MEDLINE | ID: mdl-36907119
ABSTRACT

BACKGROUND:

Optic neuritis (ON) can be an initial manifestation of neuromyelitis optica spectrum disorder (NMOSD) associated with aquaporin 4-antibody (AQP4-Ab) or myelin oligodendrocyte glycoprotein antibody (MOG-Ab)-associated disease (MOGAD). Additionally, both diseases may have overlapping paraclinical and radiological features. These diseases may have different outcomes and prognoses. We aimed to compare clinical outcomes and prognostic features of patients with NMOSD and MOGAD presenting ON as first attack, from different ethnic groups in Latin America.

METHODS:

We conducted a retrospective observational multicenter study in patients from Argentina (n = 61), Chile (n = 18), Ecuador (n = 27), Brazil (n = 30), Venezuela (n = 10) and Mexico (n = 49) with MOGAD or NMOSD related ON. Predictors of disability outcomes at last follow-up, namely visual disability (Visual Functional System Score ≥4), motor disability (permanent inability to walk further than 100 m unaided) and wheelchair dependence based on EDSS score were evaluated.

RESULTS:

After a mean disease duration of 42.7 (±40.2) months in NMOSD and 19.7 (±23.6) in MOGAD, 55% and 22% (p>0.001) experienced permanent severe visual disability (visual acuity from 20/100 to 20/200), 22% and 6% (p = 0.01) permanent motor disability and 11% and 0% (p = 0.04) had become wheelchair dependent, respectively. Older age at disease onset was a predictor of severe visual disability (OR=1,03 CI95%1.01-1.05, p = 0.03); older age at disease onset (OR=1,04 CI95%1.01-1.07, p = 0.01), higher number of relapses (OR=1,32 CI95%1.02-1.71, p = 0.03) and rituximab treatment (OR=0,36 CI95%0.14-0.90, p = 0.02) were predictors of permanent motor disability, whereas ON associated with myelitis at disease onset was a predictor of wheelchair dependency (OR=4,16, CI95%1.23-14.08, p = 0,02) in NMOSD patients. No differences were found when evaluating distinct ethnic groups (Mixed vs. Caucasian vs. Afro-descendant)

CONCLUSIONS:

NMOSD was associated with poorer clinical outcomes than MOGAD. Ethnicity was not associated with prognostic factors. Distinct predictors of permanent visual and motor disability and wheelchair dependency in NMOSD patients were found.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Optic Neuritis / Neuromyelitis Optica / Disabled Persons / Motor Disorders Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Mult Scler Relat Disord Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Optic Neuritis / Neuromyelitis Optica / Disabled Persons / Motor Disorders Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Mult Scler Relat Disord Year: 2023 Document type: Article