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Longitudinal Accumulation of Cerebral Microhemorrhages in Dominantly Inherited Alzheimer Disease

Authors :
Joseph-Mathurin, Nelly
Wang, Guoqiao
Massoumzadeh, Parinaz
Hornbeck, Russ C
Allegri, Ricardo F
Ances, Beau M
Berman, Sarah B
Brickman, Adam M
Brooks, William S
Cash, David M
Chhatwal, Jasmeer P
Chui, Helena C
Kantarci, Kejal
Correia, Stephen
Cruchaga, Carlos
Farlow, Martin R
Fox, Nick C
Fulham, Michael
Ghetti, Bernardino
Graff-Radford, Neill R
Johnson, Keith A
Karch, Celeste M
Laske, Christoph
Jack, Clifford R
Lee, Athene K W
Levin, Johannes
Masters, Colin L
Noble, James M
O'Connor, Antoinette
Perrin, Richard J
Preboske, Gregory M
Ringman, John M
Rowe, Christopher C
Salloway, Stephen
McDade, Eric
Saykin, Andrew J
Schofield, Peter R
Shimada, Hiroyuki
Shoji, Mikio
Suzuki, Kazushi
Villemagne, Victor L
Xiong, Chengjie
Yakushev, Igor
Morris, John C
Bateman, Randall J
Hassenstab, Jason
Benzinger, Tammie L S
Network, Dominantly Inherited Alzheimer
Blazey, Tyler M
Gordon, Brian A
Su, Yi
Chen, Gengsheng
Source :
Neurology 96(12), e1632-e1645 (2021). doi:10.1212/WNL.0000000000011542, Neurology, article-version (Version of Record) 3
Publication Year :
2021
Publisher :
Ovid, 2021.

Abstract

ObjectiveTo investigate the inherent clinical risks associated with the presence of cerebral microhemorrhages (CMHs) or cerebral microbleeds and characterize individuals at high risk for developing hemorrhagic amyloid-related imaging abnormality (ARIA-H), we longitudinally evaluated families with dominantly inherited Alzheimer disease (DIAD).MethodsMutation carriers (n = 310) and noncarriers (n = 201) underwent neuroimaging, including gradient echo MRI sequences to detect CMHs, and neuropsychological and clinical assessments. Cross-sectional and longitudinal analyses evaluated relationships between CMHs and neuroimaging and clinical markers of disease.ResultsThree percent of noncarriers and 8% of carriers developed CMHs primarily located in lobar areas. Carriers with CMHs were older, had higher diastolic blood pressure and Hachinski ischemic scores, and more clinical, cognitive, and motor impairments than those without CMHs. APOE ε4 status was not associated with the prevalence or incidence of CMHs. Prevalent or incident CMHs predicted faster change in Clinical Dementia Rating although not composite cognitive measure, cortical thickness, hippocampal volume, or white matter lesions. Critically, the presence of 2 or more CMHs was associated with a significant risk for development of additional CMHs over time (8.95 ± 10.04 per year).ConclusionOur study highlights factors associated with the development of CMHs in individuals with DIAD. CMHs are a part of the underlying disease process in DIAD and are significantly associated with dementia. This highlights that in participants in treatment trials exposed to drugs, which carry the risk of ARIA-H as a complication, it may be challenging to separate natural incidence of CMHs from drug-related CMHs.

Details

Language :
English
Database :
OpenAIRE
Journal :
Neurology 96(12), e1632-e1645 (2021). doi:10.1212/WNL.0000000000011542, Neurology, article-version (Version of Record) 3
Accession number :
edsair.doi.dedup.....3edb893204d0bbc0bc95a1a0a2549e28
Full Text :
https://doi.org/10.1212/WNL.0000000000011542