Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

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

Title: Cognition in patients with myelin oligodendrocyte glycoprotein antibody-associated disease: a prospective, longitudinal, multicentre study of 113 patients (CogniMOG-Study)
Authors: Passoke, S.; Stern, C.; Häußler, V.; Kümpfel, T.; Havla, J.; Engels, D.; Jarius, S.; Wildemann, B.; Korporal-Kuhnke, M.; Senel, M.; Stellmann, J.P.; Warnke, C.; Grothe, M.; Schülke, R.; Gingele, S.; Kretschmer, J.R.; Klotz, L.; Walter, A.; Then Bergh, F.; Aktas, O.; Ringelstein, M.; Ayzenberg, I.; Schwake, C.; Kleiter, I.; Sperber, P.S.; Rust, R.; Schindler, P.; Bellmann-Strobl, J.; Paul, F.; Kopp, B.; Trebst, C.; Hümmert, M.W.
Publisher Information: BMJ Publishing Group
Publication Year: 2025
Collection: Max-Delbrueck-Center for Molecular Medicine, Berlin: MDC Repository
Subject Terms: Function and Dysfunction of the Nervous System; Topic 3: Integrative Biomedicine
Description: BACKGROUND: Data 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. METHODS: The 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. RESULTS: At 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. CONCLUSIONS: Based 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.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: https://edoc.mdc-berlin.de/id/eprint/24576/1/24576oa.pdf; Cognition in patients with myelin oligodendrocyte glycoprotein antibody-associated disease: a prospective, longitudinal, multicentre study of 113 patients (CogniMOG-Study). Passoke, S., Stern, C., Häußler, V., Kümpfel, T., Havla, J., Engels, D., Jarius, S., Wildemann, B., Korporal-Kuhnke, M., Senel, M., Stellmann, J.P., Warnke, C., Grothe, M., Schülke, R., Gingele, S., Kretschmer, J.R., Klotz, L., Walter, A., Then Bergh, F., Aktas, O., Ringelstein, M., Ayzenberg, I., Schwake, C., Kleiter, I., Sperber, P.S., Rust, R., Schindler, P., Bellmann-Strobl, J., Paul, F., Kopp, B., Trebst, C. and Hümmert, M.W. Journal of Neurology Neurosurgery and Psychiatry 96 (3): e333994. March 2025; PMID:39084862; https://doi.org/10.1136/jnnp-2024-333994
DOI: 10.1136/jnnp-2024-333994
Availability: https://edoc.mdc-berlin.de/id/eprint/24576/; https://edoc.mdc-berlin.de/24576/; https://doi.org/10.1136/jnnp-2024-333994
Rights: cc_by_nc_4
Accession Number: edsbas.316A8548
Database: BASE