Is APOE ϵ4 associated with cognitive performance in early MS?

Sinah Engel, Christiane Graetz, Anke Salmen, Muthuraman Muthuraman, Gerrit Toenges, Björn Ambrosius, Antonios Bayas, Achim Berthele, Christoph Heesen, Luisa Klotz, Tania Kümpfel, Ralf A. Linker, Sven G. Meuth, Friedemann Paul, Martin Stangel, Björn Tackenberg, Florian Then Bergh, Hayrettin Tumani, Frank Weber, Brigitte WildemannUwe K. Zettl, Gisela Antony, Stefan Bittner, Sergiu Groppa, Bernhard Hemmer, Heinz Wiendl, Ralf Gold, Frauke Zipp, Christina M. Lill, Felix Luessi

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

ObjectiveTo assess the impact of APOE polymorphisms on cognitive performance in patients newly diagnosed with clinically isolated syndrome (CIS) or relapsing-remitting MS (RRMS).MethodsThis multicenter cohort study included 552 untreated patients recently diagnosed with CIS or RRMS according to the 2005 revised McDonald criteria. The single nucleotide polymorphisms rs429358 (ϵ4) and rs7412 (ϵ2) of the APOE haplotype were assessed by allelic discrimination assays. Cognitive performance was evaluated using the 3-second paced auditory serial addition test and the Multiple Sclerosis Inventory Cognition (MUSIC). Sum scores were calculated to approximate the overall cognitive performance and memory-centered cognitive functions. The impact of the APOE carrier status on cognitive performance was assessed using multiple linear regression models, also including demographic, clinical, MRI, and lifestyle factors.ResultsAPOE ϵ4 homozygosity was associated with lower overall cognitive performance, whereas no relevant association was observed for APOE ϵ4 heterozygosity or APOE ϵ2 carrier status. Furthermore, higher disability levels, MRI lesion load, and depressive symptoms were associated with lower cognitive performance. Patients consuming alcohol had higher test scores than patients not consuming alcohol. Female sex, lower disability, and alcohol consumption were associated with better performance in the memory-centered subtests of MUSIC, whereas no relevant association was observed for APOE carrier status.ConclusionAlong with parameters of a higher disease burden, APOE ϵ4 homozygosity was identified as a potential predictor of cognitive performance in this large cohort of patients with CIS and early RRMS.

Original languageEnglish
Article numbere728
JournalNeurology: Neuroimmunology and NeuroInflammation
Volume7
Issue number4
DOIs
StatePublished - 1 Jul 2020
Externally publishedYes

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