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GWAS Study

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

Reiner AP, Lettre G, Nalls MA et al.

21738479 PubMed ID
GWAS Study Type
54215 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

RA
Reiner AP
LG
Lettre G
NM
Nalls MA
GS
Ganesh SK
MR
Mathias R
AM
Austin MA
DE
Dean E
AS
Arepalli S
BA
Britton A
CZ
Chen Z
CD
Couper D
CJ
Curb JD
EC
Eaton CB
FM
Fornage M
GS
Grant SF
HT
Harris TB
HD
Hernandez D
KN
Kamatini N
KB
Keating BJ
KM
Kubo M
LA
LaCroix A
LL
Lange LA
LS
Liu S
LK
Lohman K
MY
Meng Y
ME
Mohler ER
MS
Musani S
NY
Nakamura Y
OC
O'Donnell CJ
OY
Okada Y
PC
Palmer CD
PG
Papanicolaou GJ
PK
Patel KV
SA
Singleton AB
TA
Takahashi A
TH
Tang H
TH
Taylor HA
TK
Taylor K
TC
Thomson C
YL
Yanek LR
YL
Yang L
ZE
Ziv E
ZA
Zonderman AB
FA
Folsom AR
EM
Evans MK
LY
Liu Y
BD
Becker DM
SB
Snively BM
WJ
Wilson JG
Chapter II

Abstract

Summary of the research findings

Total white blood cell (WBC) and neutrophil counts are lower among individuals of African descent due to the common African-derived "null" variant of the Duffy Antigen Receptor for Chemokines (DARC) gene. Additional common genetic polymorphisms were recently associated with total WBC and WBC sub-type levels in European and Japanese populations. No additional loci that account for WBC variability have been identified in African Americans. In order to address this, we performed a large genome-wide association study (GWAS) of total WBC and cell subtype counts in 16,388 African-American participants from 7 population-based cohorts available in the Continental Origins and Genetic Epidemiology Network. In addition to the DARC locus on chromosome 1q23, we identified two other regions (chromosomes 4q13 and 16q22) associated with WBC in African Americans (P<2.5×10(-8)). The lead SNP (rs9131) on chromosome 4q13 is located in the CXCL2 gene, which encodes a chemotactic cytokine for polymorphonuclear leukocytes. Independent evidence of the novel CXCL2 association with WBC was present in 3,551 Hispanic Americans, 14,767 Japanese, and 19,509 European Americans. The index SNP (rs12149261) on chromosome 16q22 associated with WBC count is located in a large inter-chromosomal segmental duplication encompassing part of the hydrocephalus inducing homolog (HYDIN) gene. We demonstrate that the chromosome 16q22 association finding is most likely due to a genotyping artifact as a consequence of sequence similarity between duplicated regions on chromosomes 16q22 and 1q21. Among the WBC loci recently identified in European or Japanese populations, replication was observed in our African-American meta-analysis for rs445 of CDK6 on chromosome 7q21 and rs4065321 of PSMD3-CSF3 region on chromosome 17q21. In summary, the CXCL2, CDK6, and PSMD3-CSF3 regions are associated with WBC count in African American and other populations. We also demonstrate that large inter-chromosomal duplications can result in false positive associations in GWAS.

16,388 African American individuals

Chapter III

Study Statistics

Key metrics and study information

54215
Total Participants
GWAS
Study Type
Yes
Replicated
3,551 Hispanic individuals, 14,767 Japanese ancestry individuals, 19,509 European ancestry individuals
Replication Participants
African American or Afro-Caribbean, East Asian, Hispanic or Latin American, European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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