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Qualitative Comparison of Semantic Memory Impairment in Patients with Amnestic Mild Cognitive Impairment Based on β-Amyloid Status

Authors :
Sun-Mi Lee
Jae Seung Kim
Jee Hoon Roh
Jae-Hong Lee
Jihye Hwang
Ji-Eun Kim
So Hee Park
Yun Jeong Hong
Noh Eul Han
Source :
Journal of Clinical Neurology (Seoul, Korea)
Publication Year :
2018
Publisher :
Korean Neurological Association, 2018.

Abstract

Background and purpose Semantic memory remains more stable than episodic memory across the lifespan, which makes it potentially useful as a marker for distinguishing pathological aging from normal senescence. To obtain a better understanding of the transitional stage evolving into Alzheimer's dementia (AD), we focused on the amnestic mild cognitive impairment (aMCI) stage stratified based on β-amyloid (Aβ) pathology. Methods We analyzed the raw data from Korean version of the Boston Naming Test (K-BNT) and the Controlled Oral Word Association Test (COWAT). For K-BNT, the frequencies of six error types and accuracy rates were evaluated. For a qualitative assessment of the COWAT, we computed the number of switching, number of clusters, and mean cluster size. Results The data from 217 participants were analyzed (53 normal controls, 66 with Aβ- aMCI, 56 with Aβ+ aMCI, and 42 disease controls). There were fewer semantically related errors and more semantically unrelated errors on the K-BNT in Aβ+ aMCI than in Aβ- aMCI, without a gross difference in the z score. We also found that Aβ+ aMCI showed a more prominent deficit in the number of clusters in the semantic fluency task [especially for animal names (living items)] than Aβ- aMCI. Conclusions In spite of similar clinical manifestations, Aβ+ aMCI was more similar to AD than Aβ- aMCI in terms of semantic memory disruption. Semantic memory may serve as an early indicator of brain Aβ pathology. Therefore, semantic memory dysfunction deserves more consideration in clinical practice. Longitudinal research with the follow-up data is needed.

Details

Language :
English
ISSN :
20055013 and 17386586
Volume :
15
Issue :
1
Database :
OpenAIRE
Journal :
Journal of Clinical Neurology (Seoul, Korea)
Accession number :
edsair.doi.dedup.....5d46d6b6fc857c0ede5a09ba3ff9262a