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Medial Temporal Atrophy and Memory Dysfunction in Poststroke Cognitive Impairment-No Dementia

Authors
Kim, Beom JoonOh, Mi-YoungJang, Myung SukHan, Moon-KuLee, JisungLee, JuneyoungKang, YeonwookYu, Kyung-HoLee, Byung-ChulKim, SangyunYoon, Byung-WooBae, Hee-Joon
Issue Date
Mar-2012
Publisher
KOREAN NEUROLOGICAL ASSOC
Keywords
vascular cognitive impairment; memory dysfunction; stroke; poststroke dementia
Citation
JOURNAL OF CLINICAL NEUROLOGY, v.8, no.1, pp.43 - 50
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF CLINICAL NEUROLOGY
Volume
8
Number
1
Start Page
43
End Page
50
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/105410
DOI
10.3988/jcn.2012.8.1.43
ISSN
1738-6586
Abstract
Background and Purpose It was recently reported that the prevalence of poststroke memory dysfunction might be higher than previously thought. Stroke may exist concomitantly with underlying Alzheimer's disease (AD), and so we determined whether post-stroke memory dysfunction indicates manifestation of underlying subclinical AD. Methods Of 1201 patients in a prospective cognitive assessment database, we enrolled subjects with poststroke amnestic vascular cognitive impairment-no dementia (aVCIND; n=48), poststroke nonamnestic vascular cognitive impairment-no dementia (naVCIND; n=50), and nonstroke amnestic mild cognitive impairment (aMCI; n=65). All subjects had cognitive deficits, but did not meet the criteria for dementia. A standardized neuropsychological test battery and magnetic resonance imaging were performed at least 90 days after the index stroke (mean, 473 days). Visual assessment of medial temporal atrophy (MTA) was used as a measure of underlying AD pathology. Results The MTA score was significantly lower in the naVCIND group (0.64 +/- 0.85, mean +/- SD) than in the aVCIND (1.10+/-1.08) and aMCI (1.45+/-1.13; p<0.01) groups. Multivariable ordinal logistic regression analysis revealed that compared with naVCIND, aVCIND [odds ratio (OR)=2.69; 95% confidence interval (CI)=1.21-5.99] and aMCI (OR=5.20; 95% C1=2.41-11.23) were significantly associated with increasing severity of MTA. Conclusions Our findings show that compared with poststroke naVCIND, the odds of having more-severe MTA were increased for poststroke aVCIND and nonstroke aMCI. J Clio Neurol 2012;8:43-50
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