ECTRIMS eLearning

Application of the Matthews's criteria to differentiate MS from NMOSD at disease onset in a Latin American cohort
Author(s): ,
E. Carnero Contentti
Affiliations:
Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina
,
I. Soto de Castillo
Affiliations:
Neurology Department, Hospital Universitario de Maracaibo, Maracaibo, Bolivarian Republic of Venezuela
,
V. Daccach Marques
Affiliations:
Department of Neurosciences and Behavioral Sciences, Hospital das Clínicas, Ribeirão Preto Medical School, University of de São Paulo, São Paulo, Brazil
,
V. Tkachuk
Affiliations:
Seccion de Neuroinmunologia y Enfermedades Desmielinizantes, Servicio de Neurología, Hospital de Clínicas José de San Martin
,
A. Antunes Barreira
Affiliations:
Department of Neurosciences and Behavioral Sciences, Hospital das Clínicas, Ribeirão Preto Medical School, University of de São Paulo, São Paulo, Brazil
,
A. Caride
Affiliations:
Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina
,
M.C. Castillo
Affiliations:
Neurology Department, Hospital Universitario de Maracaibo, Maracaibo, Bolivarian Republic of Venezuela
,
E. Cristiano
Affiliations:
Centro de Esclerosis Múltiple de Buenos Aires, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina
,
C. de Aquino Cruz
Affiliations:
Department of Neurosciences and Behavioral Sciences, Hospital das Clínicas, Ribeirão Preto Medical School, University of de São Paulo, São Paulo, Brazil
,
G. Braga Diégues Serva
Affiliations:
Department of Neurosciences and Behavioral Sciences, Hospital das Clínicas, Ribeirão Preto Medical School, University of de São Paulo, São Paulo, Brazil
,
R. Labarca
Affiliations:
Neurology Department, Hospital Universitario de Maracaibo, Maracaibo, Bolivarian Republic of Venezuela
,
P.A. Lopez
Affiliations:
Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina
,
J. Miguez
Affiliations:
Centro de Esclerosis Múltiple de Buenos Aires, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina
,
O. Molina
Affiliations:
Neurology Department, Hospital Universitario de Maracaibo, Maracaibo, Bolivarian Republic of Venezuela
,
D. Nadur
Affiliations:
Seccion de Neuroinmunologia y Enfermedades Desmielinizantes, Servicio de Neurología, Hospital de Clínicas José de San Martin
,
J.P. Pettinicchi
Affiliations:
Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina
,
L. Ravagnani Silva
Affiliations:
Department of Neurosciences and Behavioral Sciences, Hospital das Clínicas, Ribeirão Preto Medical School, University of de São Paulo, São Paulo, Brazil
,
L. Sampaio Barretto
Affiliations:
Department of Neurosciences and Behavioral Sciences, Hospital das Clínicas, Ribeirão Preto Medical School, University of de São Paulo, São Paulo, Brazil
J.I. Rojas
Affiliations:
Centro de Esclerosis Múltiple de Buenos Aires, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina
ECTRIMS Learn. Carnero Contentti E. 10/10/18; 229137; EP1298
Dr. Edgar Carnero Contentti
Dr. Edgar Carnero Contentti
Contributions Biography
Abstract

Abstract: EP1298

Type: Poster Sessions

Abstract Category: Clinical aspects of MS - Diagnosis and differential diagnosis

Background: An overlapping of symptoms among multiple sclerosis (MS) and neuromyelitis optica spectrum disorders (NMOSD) may be found at disease onset. Recently, magnetic resonance imaging (MRI) criteria (Matthews's criteria, MC) were described to differentiate MS from NMOSD in clinical practice. However, these criteria were not evaluated in non-Caucasian population. The aim was to evaluate these criteria in Latin American population.
Methods: medical records and brain MRIs were assessed by a blind evaluator and scored on the MC (lesions adjacent to the body of the lateral ventricle, lesions in inferior temporal lobe, S-shaped/curved U-fibre lesions and Dawson's fingers) in a Latin American cohort (Argentina, Brazil and Venezuela) of patients with MS and NMOSD (previously diagnosed by current validated diagnosis criteria and used as gold standard). MC sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were determined.
Results: We included 282 patients (MS = 188 and NMOSD = 94, ratio 2:1). Patients from Argentina (MS = 92, NMOSD = 38), Brazil (MS = 55, NMOSD = 27) and Venezuela (MS = 29, NMOSD = 41) were evaluated at disease onset. The MC applied to the entire cohort at disease onset showed a 97.8% sensitivity, 82.9% specificity, 92.0% PPV, and 95.1% NPV in differentiate MS from NMOSD. The sub-analysis applied only to non-Caucasian populations (mestizos, natives and zambos, MS = 89 and NMOSD = 47) showed a 100% sensitivity, 80.8% specificity, 90.8% PPV, and 100% NPV.
Conclusion: These findings suggest that the MC distinguished MS from NMOSD at disease onset in a Latin American cohort.
Disclosure: None of the authors has any potential financial conflict of interest related to this poster

Abstract: EP1298

Type: Poster Sessions

Abstract Category: Clinical aspects of MS - Diagnosis and differential diagnosis

Background: An overlapping of symptoms among multiple sclerosis (MS) and neuromyelitis optica spectrum disorders (NMOSD) may be found at disease onset. Recently, magnetic resonance imaging (MRI) criteria (Matthews's criteria, MC) were described to differentiate MS from NMOSD in clinical practice. However, these criteria were not evaluated in non-Caucasian population. The aim was to evaluate these criteria in Latin American population.
Methods: medical records and brain MRIs were assessed by a blind evaluator and scored on the MC (lesions adjacent to the body of the lateral ventricle, lesions in inferior temporal lobe, S-shaped/curved U-fibre lesions and Dawson's fingers) in a Latin American cohort (Argentina, Brazil and Venezuela) of patients with MS and NMOSD (previously diagnosed by current validated diagnosis criteria and used as gold standard). MC sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were determined.
Results: We included 282 patients (MS = 188 and NMOSD = 94, ratio 2:1). Patients from Argentina (MS = 92, NMOSD = 38), Brazil (MS = 55, NMOSD = 27) and Venezuela (MS = 29, NMOSD = 41) were evaluated at disease onset. The MC applied to the entire cohort at disease onset showed a 97.8% sensitivity, 82.9% specificity, 92.0% PPV, and 95.1% NPV in differentiate MS from NMOSD. The sub-analysis applied only to non-Caucasian populations (mestizos, natives and zambos, MS = 89 and NMOSD = 47) showed a 100% sensitivity, 80.8% specificity, 90.8% PPV, and 100% NPV.
Conclusion: These findings suggest that the MC distinguished MS from NMOSD at disease onset in a Latin American cohort.
Disclosure: None of the authors has any potential financial conflict of interest related to this poster

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