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GWAS Study

Identifying risk loci for FTD and shared genetic component with ALS: A large-scale multitrait association analysis.

Chen K, Gao T, Liu Y et al.

37979250 PubMed ID
GWAS Study Type
12928 Participants
167 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CK
Chen K
GT
Gao T
LY
Liu Y
ZK
Zhu K
WT
Wang T
ZP
Zeng P
Chapter II

Abstract

Summary of the research findings

Current genome-wide association studies of frontotemporal dementia (FTD) are underpowered due to limited samples. Further, common genetic etiologies between FTD and amyotrophic lateral sclerosis (ALS) remain unknown. Using the largest summary statistics of FTD (3526 cases and 9402 controls) and ALS (27,205 cases and 110,881 controls), we found a significant genetic correlation between them (rˆg = 0.637, P = 0.032) and identified 190 FTD-related variants within 5 loci (3p22.1, 5q35.1, 9p21.2, 19p13.11, and 20q13.13). Among these, ALS and FTD had causal variants in 9p21.2 and 19p13.11. Moreover, MOBP (3p22.1), C9orf72 (9p21.2), MOB3B (9p21.2), UNC13A (19p13.11), SLC9A8 (20q13.13), SNAI1 (20q13.13), and SPATA2 (20q13.13) were discovered by both SNP- and gene-level analyses, which together discovered 15 FTD-associated genes, with 10 not detected before (IFNK, RNF114, SLC9A8, SPATA2, SNAI1, SCFD1, POLDIP2, TMEM97, G2E3, and PIGW). Functional analyses showed these genes were enriched in heart left ventricle, kidney cortex, and some brain regions. Overall, this study provides insights into genetic determinants of FTD and shared genetic etiology underlying FTD and ALS.

at least 3,526 European ancestry cases, at least 9,402 European ancestry controls (MTAG boosted by amyotrophic lateral sclerosis samples)

Chapter III

Study Statistics

Key metrics and study information

12928
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

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