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Prognostic relevance of quantitative and longitudinal MOG antibody testing in patients with MOGAD: a multicentre retrospective study.

Authors :
Gastaldi, Matteo
Foiadelli, Thomas
Greco, Giacomo
Scaranzin, Silvia
Rigoni, Eleonora
Masciocchi, Stefano
Ferrari, Sergio
Mancinelli, Chiara
Brambilla, Laura
Mancardi, Margherita
Giacomini, Thea
Ferraro, Diana
Corte, Marida Della
Gallo, Antonio
Di Filippo, Massimiliano
Benedetti, Luana
Novi, Giovanni
Versino, Maurizio
Banfi, Paola
Iorio, Raffaele
Source :
Journal of Neurology, Neurosurgery & Psychiatry; Mar2023, Vol. 94 Issue 3, p201-210, 10p
Publication Year :
2023

Abstract

<bold>Background: </bold>IgG antibodies against myelin oligodendrocyte glycoprotein (MOG-IgG) define a subset of associated disorders (myelin oligodendrocyte glycoprotein associated disorders (MOGAD)) that can have a relapsing course. However, information on relapse predictors is scarce. The utility of retesting MOG-IgG over time and measuring their titres is uncertain. We aimed to evaluate the clinical relevance of longitudinal MOG-IgG titre measurement to predict relapses in patients with MOGAD.<bold>Methods: </bold>In this retrospective multicentre Italian cohort study, we recruited patients with MOGAD and available longitudinal samples (at least one >3 months after disease onset) and tested them with a live cell-based assay with endpoint titration (1:160 cut-off). Samples were classified as 'attack' (within 30 days since a disease attack (n=59, 17%)) and 'remission' (≥31 days after attack (n=295, 83%)).<bold>Results: </bold>We included 102 patients with MOGAD (57% adult and 43% paediatric) with a total of 354 samples (83% from remission and 17% from attack). Median titres were higher during attacks (1:1280 vs 1:640, p=0.001). Median onset titres did not correlate with attack-related disability, age or relapses. Remission titres were higher in relapsing patients (p=0.02). When considering the first remission sample available for each patient, titres >1:2560 were predictors of relapsing course in survival (log rank, p<0.001) and multivariate analysis (p<0.001, HR: 10.9, 95% CI 3.4 to 35.2). MOG-IgG seroconversion to negative was associated with a 95% relapse incidence rate reduction (incidence rate ratio: 0.05, p<0.001).<bold>Conclusions: </bold>Persistent MOG-IgG positivity and high remission titres are associated with an increased relapse risk. Longitudinal MOG-IgG titres could be useful to stratify patients to be treated with long term immunosuppression. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00223050
Volume :
94
Issue :
3
Database :
Complementary Index
Journal :
Journal of Neurology, Neurosurgery & Psychiatry
Publication Type :
Academic Journal
Accession number :
162418940
Full Text :
https://doi.org/10.1136/jnnp-2022-330237