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July 03, 2018; 91 (1) Article

Associations between lesions and domain-specific cognitive decline in poststroke dementia

Chathuri Yatawara, Kok Pin Ng, Russell Chander, Nagaendran Kandiah
First published May 25, 2018, DOI: https://doi.org/10.1212/WNL.0000000000005734
Chathuri Yatawara
From the Department of Neurology (C.Y., K.P.N., R.C., N.K.), National Neuroscience Institute; and Duke-NUS (N.K.), Singapore.
PhD
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Kok Pin Ng
From the Department of Neurology (C.Y., K.P.N., R.C., N.K.), National Neuroscience Institute; and Duke-NUS (N.K.), Singapore.
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Russell Chander
From the Department of Neurology (C.Y., K.P.N., R.C., N.K.), National Neuroscience Institute; and Duke-NUS (N.K.), Singapore.
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Nagaendran Kandiah
From the Department of Neurology (C.Y., K.P.N., R.C., N.K.), National Neuroscience Institute; and Duke-NUS (N.K.), Singapore.
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Associations between lesions and domain-specific cognitive decline in poststroke dementia
Chathuri Yatawara, Kok Pin Ng, Russell Chander, Nagaendran Kandiah
Neurology Jul 2018, 91 (1) e45-e54; DOI: 10.1212/WNL.0000000000005734

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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.

Glossary

AD=
Alzheimer disease;
BC=
bias-corrected;
CI=
confidence interval;
IQCODE=
Informant Questionnaire of Cognitive Decline in the Elderly;
mRS=
modified Rankin Scale;
OR=
odds ratio;
PHQ-9=
Patient Health Questionnaire;
PSD=
poststroke dementia;
WMH=
white matter hyperintensities

Footnotes

  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Received November 6, 2017.
  • Accepted in final form April 3, 2018.
  • © 2018 American Academy of Neurology
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