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GWAS Study

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.

Evans DS, Avery CL, Nalls MA et al.

27577874 PubMed ID
GWAS Study Type
53438 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ED
Evans DS
AC
Avery CL
NM
Nalls MA
LG
Li G
BJ
Barnard J
SE
Smith EN
TT
Tanaka T
BA
Butler AM
BS
Buxbaum SG
AA
Alonso A
AD
Arking DE
BG
Berenson GS
BJ
Bis JC
BS
Buyske S
CC
Carty CL
CW
Chen W
CM
Chung MK
CS
Cummings SR
DR
Deo R
EC
Eaton CB
FE
Fox ER
HS
Heckbert SR
HG
Heiss G
HL
Hindorff LA
HW
Hsueh WC
IA
Isaacs A
JY
Jamshidi Y
KK
Kerr KF
LF
Liu F
LY
Liu Y
LK
Lohman KK
MJ
Magnani JW
MJ
Maher JF
MR
Mehra R
MY
Meng YA
MS
Musani SK
NC
Newton-Cheh C
NK
North KE
PB
Psaty BM
RS
Redline S
RJ
Rotter JI
SR
Schnabel RB
SN
Schork NJ
SR
Shohet RV
SA
Singleton AB
SJ
Smith JD
SE
Soliman EZ
SS
Srinivasan SR
TH
Taylor HA
VW
Van Wagoner DR
WJ
Wilson JG
YT
Young T
ZZ
Zhang ZM
ZA
Zonderman AB
EM
Evans MK
FL
Ferrucci L
MS
Murray SS
TG
Tranah GJ
WE
Whitsel EA
RA
Reiner AP
SN
Sotoodehnia N
Chapter II

Abstract

Summary of the research findings

The electrocardiographic QRS duration, a measure of ventricular depolarization and conduction, is associated with cardiovascular mortality. While single nucleotide polymorphisms (SNPs) associated with QRS duration have been identified at 22 loci in populations of European descent, the genetic architecture of QRS duration in non-European populations is largely unknown. We therefore performed a genome-wide association study (GWAS) meta-analysis of QRS duration in 13,031 African Americans from ten cohorts and a transethnic GWAS meta-analysis with additional results from populations of European descent. In the African American GWAS, a single genome-wide significant SNP association was identified (rs3922844, P = 4 × 10-14) in intron 16 of SCN5A, a voltage-gated cardiac sodium channel gene. The QRS-prolonging rs3922844 C allele was also associated with decreased SCN5A RNA expression in human atrial tissue (P = 1.1 × 10-4). High density genotyping revealed that the SCN5A association region in African Americans was confined to intron 16. Transethnic GWAS meta-analysis identified novel SNP associations on chromosome 18 in MYL12A (rs1662342, P = 4.9 × 10-8) and chromosome 1 near CD1E and SPTA1 (rs7547997, P = 7.9 × 10-9). The 22 QRS loci previously identified in populations of European descent were enriched for significant SNP associations with QRS duration in African Americans (P = 9.9 × 10-7), and index SNP associations in or near SCN5A, SCN10A, CDKN1A, NFIA, HAND1, TBX5 and SETBP1 replicated in African Americans. In summary, rs3922844 was associated with QRS duration and SCN5A expression, two novel QRS loci were identified using transethnic meta-analysis, and a significant proportion of QRS-SNP associations discovered in populations of European descent were transferable to African Americans when adequate power was achieved.

up to 13,031 African American individuals, 40,407 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

53438
Total Participants
GWAS
Study Type
No
Replicated
African American or Afro-Caribbean, European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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