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GWAS Study

Genome sequence analyses identify novel risk loci for multiple system atrophy.

Chia R, Ray A, Shah Z et al.

38701790 PubMed ID
GWAS Study Type
8016 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CR
Chia R
RA
Ray A
SZ
Shah Z
DJ
Ding J
RP
Ruffo P
FM
Fujita M
MV
Menon V
SS
Saez-Atienzar S
RP
Reho P
KK
Kaivola K
WR
Walton RL
RR
Reynolds RH
KR
Karra R
SS
Sait S
AF
Akcimen F
DM
Diez-Fairen M
AI
Alvarez I
FA
Fanciulli A
SN
Stefanova N
SK
Seppi K
DS
Duerr S
LF
Leys F
KF
Krismer F
SV
Sidoroff V
ZA
Zimprich A
PW
Pirker W
RO
Rascol O
FA
Foubert-Samier A
MW
Meissner WG
TF
Tison F
PT
Pavy-Le Traon A
PM
Pellecchia MT
BP
Barone P
RM
Russillo MC
MJ
Marín-Lahoz J
KJ
Kulisevsky J
TS
Torres S
MP
Mir P
PM
Periñán MT
PC
Proukakis C
CV
Chelban V
WL
Wu L
GY
Goh YY
PL
Parkkinen L
HM
Hu MT
KC
Kobylecki C
SJ
Saxon JA
RS
Rollinson S
GE
Garland E
BI
Biaggioni I
LI
Litvan I
RI
Rubio I
AR
Alcalay RN
KK
Kwei KT
LS
Lubbe SJ
MQ
Mao Q
FM
Flanagan ME
CR
Castellani RJ
KV
Khurana V
NA
Ndayisaba A
CA
Calvo A
MG
Mora G
CA
Canosa A
FG
Floris G
BR
Bohannan RC
MA
Moore A
NL
Norcliffe-Kaufmann L
PJ
Palma JA
KH
Kaufmann H
KC
Kim C
IM
Iba M
ME
Masliah E
DT
Dawson TM
RL
Rosenthal LS
PA
Pantelyat A
AM
Albert MS
PO
Pletnikova O
TJ
Troncoso JC
IJ
Infante J
LC
Lage C
SP
Sánchez-Juan P
SG
Serrano GE
BT
Beach TG
PP
Pastor P
MH
Morris HR
AD
Albani D
CJ
Clarimon J
WG
Wenning GK
HJ
Hardy JA
RM
Ryten M
TE
Topol E
TA
Torkamani A
CA
Chiò A
BD
Bennett DA
DJ
De Jager PL
LP
Low PA
SW
Singer W
CW
Cheshire WP
WZ
Wszolek ZK
DD
Dickson DW
TB
Traynor BJ
GJ
Gibbs JR
DC
Dalgard CL
RO
Ross OA
HH
Houlden H
SS
Scholz SW
Chapter II

Abstract

Summary of the research findings

Multiple system atrophy (MSA) is an adult-onset, sporadic synucleinopathy characterized by parkinsonism, cerebellar ataxia, and dysautonomia. The genetic architecture of MSA is poorly understood, and treatments are limited to supportive measures. Here, we performed a comprehensive analysis of whole genome sequence data from 888 European-ancestry MSA cases and 7,128 controls to systematically investigate the genetic underpinnings of this understudied neurodegenerative disease. We identified four significantly associated risk loci using a genome-wide association study approach. Transcriptome-wide association analyses prioritized USP38-DT, KCTD7, and lnc-KCTD7-2 as novel susceptibility genes for MSA within these loci, and single-nucleus RNA sequence analysis found that the associated variants acted as cis-expression quantitative trait loci for multiple genes across neuronal and glial cell types. In conclusion, this study highlights the role of genetic determinants in the pathogenesis of MSA, and the publicly available data from this study represent a valuable resource for investigating synucleinopathies.

888 European ancestry cases, 7,128 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

8016
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Austria, U.S., Italy, U.K., France, Spain
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.