Cognition in patients with myelin oligodendrocyte glycoprotein antibody-associated disease: a prospective, longitudinal, multicentre study of 113 patients (CogniMOG-Study)

Author:

Passoke SarahORCID,Stern Carlotta,Häußler VivienORCID,Kümpfel TaniaORCID,Havla JoachimORCID,Engels DanielORCID,Jarius Sven,Wildemann Brigitte,Korporal-Kuhnke Mirjam,Senel MakbuleORCID,Stellmann Jan-PatrickORCID,Warnke ClemensORCID,Grothe Matthias,Schülke Rasmus,Gingele StefanORCID,Kretschmer Julian Reza,Klotz Luisa,Walter Annette,Then Bergh Florian,Aktas Orhan,Ringelstein MariusORCID,Ayzenberg Ilya,Schwake Carolin,Kleiter Ingo,Sperber Pia SophieORCID,Rust Rebekka,Schindler Patrick,Bellmann-Strobl Judith,Paul Friedemann,Kopp Bruno,Trebst Corinna,Hümmert Martin WORCID

Abstract

BackgroundData on cognition in patients with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) are limited to studies with small sample sizes. Therefore, we aimed to analyse the extent, characteristics and the longitudinal course of potential cognitive deficits in patients with MOGAD.MethodsThe CogniMOG-Study is a prospective, longitudinal and multicentre observational study of 113 patients with MOGAD. Individual cognitive performance was assessed using the Paced Auditory Serial Addition Task (PASAT), the Symbol Digit Modalities Test (SDMT) and the Multiple Sclerosis Inventory Cognition (MuSIC), which are standardised against normative data from healthy controls. Cognitive performance was assessed at baseline and at 1-year and 2-year follow-up assessments. Multiple linear regression was used to analyse demographic and clinical predictors of cognitive deficits identified in previous correlation analyses.ResultsAt baseline, the study sample of MOGAD patients showed impaired standardised performance on MuSIC semantic fluency (mean=−0.29, 95% CI (−0.47 to −0.12)) and MuSIC congruent speed (mean=−0.73, 95% CI (−1.23 to −0.23)). Around 1 in 10 patients showed deficits in two or more cognitive measures (11%). No decline in cognition was observed during the 1-year and 2-year follow-up period. Cerebral lesions were found to be negatively predictive for SDMT (B=−8.85, 95% CI (−13.57 to −4.14)) and MuSIC semantic fluency (B=−4.17, 95% CI (−6.10 to −2.25)) test performance.ConclusionsBased on these data, we conclude that MOGAD patients show reduced visuomotor processing speed and semantic fluency to the extent that the disease burden includes cerebral lesions.

Publisher

BMJ

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