Associations between lesions and domain-specific cognitive decline in poststroke dementia
Abstract
Objective
To investigate whether the effect of prestroke and stroke-related lesions on incident poststroke dementia (PSD) is mediated by a unique pattern of domain-specific cognitive impairment, and the relative strength of these anatomical–cognitive associations in predicting incident PSD.
Methods
In this incident case-control study (n = 150), we defined incident cases as acute stroke patients who developed PSD and controls as acute stroke patients who remained free from dementia at a 6 month follow-up, matched on age, prestroke cognitive status, and number of stroke-related lesions. MRI was performed at initial clinical presentation; neuropsychological assessments and clinical diagnosis of PSD was performed 6 months poststroke. Moderated mediation analysis evaluated the interactions among PSD, anatomical lesions, cognitive domains, and individual demographic and medical characteristics.
Results
Compared to stroke-related lesions, prestroke lesions were associated with the widest range of cognitive domain impairments and had stronger clinical utility in predicting incident PSD. Specifically, global cortical atrophy (GCA) and deep white matter hyperintensities (WMH) were indirectly associated with PSD by disrupting executive functions, memory, and language. Acute infarcts were indirectly associated with PSD by disrupting executive functions and language. The strongest mediator was executive dysfunction, increasing risk of PSD in patients with deep WMH, GCA, and large infarcts by more than 9 times, with sex and educational attainment moderating the magnitude of association. Periventricular WMH were directly associated with incident PSD but not mediated by deficits in cognitive domains.
Conclusion
We provide an anatomical–cognitive framework that can be applied to stratify patients at highest risk of PSD and to guide personalized interventions.
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Information & Authors
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Copyright
© 2018 American Academy of Neurology.
Publication History
Received: November 6, 2017
Accepted: April 3, 2018
Published online: May 25, 2018
Published in print: July 3, 2018
Disclosure
The authors report no disclosures relevant to the manuscript. Go to Neurology.org/N for full disclosures.
Study Funding
A*STAR Biomedical Research Council, Singapore (BMRC 04/1/36/372).
Authors
Author Contributions
Dr. Yatawara: study concept and design, statistical analysis, and drafting manuscript. K.P. Pin: drafting manuscript and revising manuscript for intellectual content. R. Chander: data management and drafting manuscript. N. Kandiah: study design and revising manuscript for intellectual content.
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