Menu
GWAS Study

Ethnic differences in the frequency of β-amyloid deposition in cognitively normal individuals.

Kim J, Jung SH, Choe YS et al.

35366586 PubMed ID
GWAS Study Type
244 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KJ
Kim J
JS
Jung SH
CY
Choe YS
KS
Kim S
KB
Kim B
KH
Kim HR
SS
Son SJ
HC
Hong CH
ND
Na DL
KH
Kim HJ
CS
Cho SJ
WH
Won HH
SS
Seo SW
Chapter II

Abstract

Summary of the research findings

We investigated which factors might explain the differences between the frequencies of brain β-amyloid (Aβ) deposition in Korean and European cognitively normal individuals (CNs). We recruited 434 Korean CNs from the Samsung Medical Center (SMC) and 323 European CNs from the US Alzheimer's Disease Neuroimaging Initiative (ADNI). The Korean CNs showed lower education duration (11.8 ± 4.8 years vs. 16.8 ± 2.5 years, p < 0.001) than the European CNs. The frequency of Aβ (+) was higher in the European CNs (32.8%) than in the Korean CNs (20.0%; p < 0.001). In the SMC genome-wide association study (GWAS), 10 variants (including rs7481773 on chromosome 11, located near the brain-derived neurotrophic factor gene) exceeded the genome-wide significance level (p < 5 × 10-8). Especially, rs7481773 carriers showed more rapid decline in memory function than non-carriers (p = 0.048). However, this association was not observed in the ADNI GWAS. Our findings suggested that the different frequencies of Aβ (+) between CN Koreans and Europeans might be related to decreased cognitive reserve or genetic factors.

175 Korean ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

244
Total Participants
GWAS
Study Type
Yes
Replicated
69 Korean ancestry individuals
Replication Participants
East Asian, European
Ancestry
Republic of Korea
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.