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GWAS Study

Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.

Jain D, Hodonsky CJ, Schick UM et al.

28158719 PubMed ID
GWAS Study Type
19009 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

JD
Jain D
HC
Hodonsky CJ
SU
Schick UM
MJ
Morrison JV
MS
Minnerath S
BL
Brown L
SC
Schurmann C
LY
Liu Y
AP
Auer PL
LC
Laurie CA
TK
Taylor KD
BB
Browning BL
PG
Papanicolaou G
BS
Browning SR
LR
Loos RJF
NK
North KE
TB
Thyagarajan B
LC
Laurie CC
TT
Thornton TA
ST
Sofer T
RA
Reiner AP
Chapter II

Abstract

Summary of the research findings

Circulating white blood cell (WBC) counts (neutrophils, monocytes, lymphocytes, eosinophils, basophils) differ by ethnicity. The genetic factors underlying basal WBC traits in Hispanics/Latinos are unknown. We performed a genome-wide association study of total WBC and differential counts in a large, ethnically diverse US population sample of Hispanics/Latinos ascertained by the Hispanic Community Health Study and Study of Latinos (HCHS/SOL). We demonstrate that several previously known WBC-associated genetic loci (e.g. the African Duffy antigen receptor for chemokines null variant for neutrophil count) are generalizable to WBC traits in Hispanics/Latinos. We identified and replicated common and rare germ-line variants at FLT3 (a gene often somatically mutated in leukemia) associated with monocyte count. The common FLT3 variant rs76428106 has a large allele frequency differential between African and non-African populations. We also identified several novel genetic loci involving or regulating hematopoietic transcription factors (CEBPE-SLC7A7, CEBPA and CRBN-TRNT1) associated with basophil count. The minor allele of the CEBPE variant associated with lower basophil count has been previously associated with Amerindian ancestry and higher risk of acute lymphoblastic leukemia in Hispanics. Together, these data suggest that germline genetic variation affecting transcriptional and signaling pathways that underlie WBC development and lineage specification can contribute to inter-individual as well as ethnic differences in peripheral blood cell counts (normal hematopoiesis) in addition to susceptibility to leukemia (malignant hematopoiesis).

up to 11,809 Hispanic/Latino American individuals

Chapter III

Study Statistics

Key metrics and study information

19009
Total Participants
GWAS
Study Type
Yes
Replicated
up to 7,200 Hispanic/Latino American individuals
Replication Participants
Hispanic or Latin American
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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