APOE-ɛ4, white matter hyperintensities, and cognition in Alzheimer and Lewy body dementia

Saeed Mirza, Saira and Saeed, Usman and Knight, Jo and Ramirez, Joel and Stuss, Donald and Keith, Julia and Nestor, Sean M. and Yu, Di and Swardfager, Walter and Rogaeva, Ekaterina and George-Hyslop, Peter St. and Black, Sandra E. and Masellis, Mario (2019) APOE-ɛ4, white matter hyperintensities, and cognition in Alzheimer and Lewy body dementia. Neurology, 93 (19). e1807-e1819. ISSN 0028-3878

[thumbnail of Neurology_2018_946202_Mirza_May_13_2019_Revised_clean]
Text (Neurology_2018_946202_Mirza_May_13_2019_Revised_clean)
Neurology_2018_946202_Mirza_May_13_2019_Revised_clean.pdf - Accepted Version
Available under License Creative Commons Attribution.

Download (511kB)

Abstract

Objective To determine if APOE ε4 influences the association between white matter hyperintensities (WMH) and cognitive impairment in Alzheimer disease (AD) and dementia with Lewy bodies (DLB). Methods A total of 289 patients (AD = 239; DLB = 50) underwent volumetric MRI, neuropsychological testing, and APOE ε4 genotyping. Total WMH volumes were quantified. Neuropsychological test scores were included in a confirmatory factor analysis to identify cognitive domains encompassing attention/executive functions, learning/memory, and language, and factor scores for each domain were calculated per participant. After testing interactions between WMH and APOE ε4 in the full sample, we tested associations of WMH with factor scores using linear regression models in APOE ε4 carriers (n = 167) and noncarriers (n = 122). We hypothesized that greater WMH volume would relate to worse cognition more strongly in APOE ε4 carriers. Findings were replicated in 198 patients with AD from the Alzheimer's Disease Neuroimaging Initiative (ADNI-I), and estimates from both samples were meta-analyzed. Results A significant interaction was observed between WMH and APOE ε4 for language, but not for memory or executive functions. Separate analyses in APOE ε4 carriers and noncarriers showed that greater WMH volume was associated with worse attention/executive functions, learning/memory, and language in APOE ε4 carriers only. In ADNI-I, greater WMH burden was associated with worse attention/executive functions and language in APOE ε4 carriers only. No significant associations were observed in noncarriers. Meta-analyses showed that greater WMH volume was associated with worse performance on all cognitive domains in APOE ε4 carriers only. Conclusion APOE ε4 may influence the association between WMH and cognitive performance in AD and DLB.

Item Type:
Journal Article
Journal or Publication Title:
Neurology
Uncontrolled Keywords:
/dk/atira/pure/subjectarea/asjc/2700/2728
Subjects:
?? clinical neurology ??
ID Code:
136523
Deposited By:
Deposited On:
13 Sep 2019 10:00
Refereed?:
Yes
Published?:
Published
Last Modified:
31 Dec 2023 01:07