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GWAS Study

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.

Barc J, Tadros R, Glinge C et al.

35210625 PubMed ID
GWAS Study Type
12821 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BJ
Barc J
TR
Tadros R
GC
Glinge C
CD
Chiang DY
JM
Jouni M
SF
Simonet F
JS
Jurgens SJ
BM
Baudic M
NM
Nicastro M
PF
Potet F
OJ
Offerhaus JA
WR
Walsh R
CS
Choi SH
VA
Verkerk AO
MY
Mizusawa Y
AS
Anys S
MD
Minois D
AM
Arnaud M
DJ
Duchateau J
WY
Wijeyeratne YD
MA
Muir A
PM
Papadakis M
CS
Castelletti S
TM
Torchio M
OC
Ortuño CG
LJ
Lacunza J
GD
Giachino DF
CN
Cerrato N
MR
Martins RP
CO
Campuzano O
VD
Van Dooren S
TA
Thollet A
KF
Kyndt F
MA
Mazzanti A
CN
Clémenty N
BA
Bisson A
CA
Corveleyn A
SB
Stallmeyer B
DS
Dittmann S
SJ
Saenen J
NA
Noël A
HS
Honarbakhsh S
RB
Rudic B
MH
Marzak H
RM
Rowe MK
FC
Federspiel C
LP
Le Page S
PL
Placide L
MA
Milhem A
BH
Barajas-Martinez H
BB
Beckmann BM
KI
Krapels IP
SJ
Steinfurt J
WB
Winkel BG
JR
Jabbari R
SM
Shoemaker MB
BB
Boukens BJ
ŠD
Škorić-Milosavljević D
BH
Bikker H
MF
Manevy F
LP
Lichtner P
RM
Ribasés M
MT
Meitinger T
MM
Müller-Nurasyid M
VJ
Veldink JH
VD
van den Berg LH
VD
Van Damme P
CD
Cusi D
LC
Lanzani C
RS
Rigade S
CE
Charpentier E
BE
Baron E
BS
Bonnaud S
LS
Lecointe S
DA
Donnart A
LM
Le Marec H
CS
Chatel S
KM
Karakachoff M
BS
Bézieau S
LB
London B
TJ
Tfelt-Hansen J
RD
Roden D
OK
Odening KE
CM
Cerrone M
CL
Chinitz LA
VP
Volders PG
VD
van de Berg MP
LG
Laurent G
FL
Faivre L
AC
Antzelevitch C
KS
Kääb S
AA
Arnaout AA
DJ
Dupuis JM
PJ
Pasquie JL
BO
Billon O
RJ
Roberts JD
JL
Jesel L
BM
Borggrefe M
LP
Lambiase PD
MJ
Mansourati J
LB
Loeys B
LA
Leenhardt A
GP
Guicheney P
MP
Maury P
SE
Schulze-Bahr E
RT
Robyns T
BJ
Breckpot J
BD
Babuty D
PS
Priori SG
NC
Napolitano C
DA
de Asmundis C
BP
Brugada P
BR
Brugada R
AE
Arbelo E
BJ
Brugada J
MP
Mabo P
BN
Behar N
GC
Giustetto C
MM
Molina MS
GJ
Gimeno JR
HC
Hasdemir C
SP
Schwartz PJ
CL
Crotti L
MP
McKeown PP
SS
Sharma S
BE
Behr ER
HM
Haissaguerre M
SF
Sacher F
RC
Rooryck C
TH
Tan HL
RC
Remme CA
PP
Postema PG
DM
Delmar M
EP
Ellinor PT
LS
Lubitz SA
GJ
Gourraud JB
TM
Tanck MW
GA
George AL
MC
MacRae CA
BP
Burridge PW
DC
Dina C
PV
Probst V
WA
Wilde AA
SJ
Schott JJ
RR
Redon R
BC
Bezzina CR
Chapter II

Abstract

Summary of the research findings

Brugada syndrome (BrS) is a cardiac arrhythmia disorder associated with sudden death in young adults. With the exception of SCN5A, encoding the cardiac sodium channel NaV1.5, susceptibility genes remain largely unknown. Here we performed a genome-wide association meta-analysis comprising 2,820 unrelated cases with BrS and 10,001 controls, and identified 21 association signals at 12 loci (10 new). Single nucleotide polymorphism (SNP)-heritability estimates indicate a strong polygenic influence. Polygenic risk score analyses based on the 21 susceptibility variants demonstrate varying cumulative contribution of common risk alleles among different patient subgroups, as well as genetic associations with cardiac electrical traits and disorders in the general population. The predominance of cardiac transcription factor loci indicates that transcriptional regulation is a key feature of BrS pathogenesis. Furthermore, functional studies conducted on MAPRE2, encoding the microtubule plus-end binding protein EB2, point to microtubule-related trafficking effects on NaV1.5 expression as a new underlying molecular mechanism. Taken together, these findings broaden our understanding of the genetic architecture of BrS and provide new insights into its molecular underpinnings.

2,820 European ancestry cases, 10,001 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

12821
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Canada, Netherlands, Turkey, U.S., Belgium, Denmark, Italy, U.K., France, Germany, Spain
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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