Menu
Currency
GWAS Study

Genome and transcriptome-wide association studies identify multiple novel loci for dementia with grain in Japanese.

Mitsumori R, Ozaki K, Saito Y et al.

41402580 PubMed ID
GWAS Study Type
12619 Participants
61 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MR
Mitsumori R
OK
Ozaki K
SY
Saito Y
SD
Shigemizu D
IA
Iwata A
MS
Murayama S
AM
Akishita M
AT
Arai T
NS
Niida S
TK
Toba K
Chapter II

Abstract

Summary of the research findings

Argyrophilic grain (AG) is a common neurodegenerative accumulation of 4 repeat tau in dendritic spine. Dementia with grain (DG) is defined as AGs with a sole pathological basis for cognitive decline. As with other multifactorial diseases, DG could result from interactions of environmental and genetic factors. However, the genetic basis of DG is largely unknown. To clarify the genetic architecture of DG pathogenesis, we conducted a genome-wide association study (GWAS) with 214 DG cases versus 12,405 controls. We have identified a candidate locus associated with the risk of DG, the SVIL locus on chromosome 10, with genome-wide significance (rs11595141, P = 4.86 × 10-8) in the GWAS. Transcriptome-wide association analysis using summary statistics for DG-GWAS identified DAPK2 (PTWAS = 3.68 × 10-5) as a novel candidate causal gene for DG pathogenesis in the brain frontal cortex. The genetic association analysis for the APOE locus revealed that the APOE allele did not affect DG pathogenesis. We also identified new variants in the MAPT encoding tau protein that could potentially affect DG pathology. This is the first GWAS for DG, and our genetic findings provide biological and clinical insights into the pathogenesis of DG.

214 Japanese ancestry cases, 12,405 Japanese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

12619
Total Participants
GWAS
Study Type
No
Replicated
East Asian
Ancestry
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.