TY - JOUR
T1 - Is APOE ϵ4 associated with cognitive performance in early MS?
AU - Engel, Sinah
AU - Graetz, Christiane
AU - Salmen, Anke
AU - Muthuraman, Muthuraman
AU - Toenges, Gerrit
AU - Ambrosius, Björn
AU - Bayas, Antonios
AU - Berthele, Achim
AU - Heesen, Christoph
AU - Klotz, Luisa
AU - Kümpfel, Tania
AU - Linker, Ralf A.
AU - Meuth, Sven G.
AU - Paul, Friedemann
AU - Stangel, Martin
AU - Tackenberg, Björn
AU - Bergh, Florian Then
AU - Tumani, Hayrettin
AU - Weber, Frank
AU - Wildemann, Brigitte
AU - Zettl, Uwe K.
AU - Antony, Gisela
AU - Bittner, Stefan
AU - Groppa, Sergiu
AU - Hemmer, Bernhard
AU - Wiendl, Heinz
AU - Gold, Ralf
AU - Zipp, Frauke
AU - Lill, Christina M.
AU - Luessi, Felix
N1 - Publisher Copyright:
© American Academy of Neurology.
PY - 2020/7/1
Y1 - 2020/7/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85084894700&partnerID=8YFLogxK
U2 - 10.1212/NXI.0000000000000728
DO - 10.1212/NXI.0000000000000728
M3 - Article
C2 - 32358224
AN - SCOPUS:85084894700
SN - 2332-7812
VL - 7
JO - Neurology: Neuroimmunology and NeuroInflammation
JF - Neurology: Neuroimmunology and NeuroInflammation
IS - 4
M1 - e728
ER -