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GWAS Study

A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.

Lutz SM, Cho MH, Young K et al.

26634245 PubMed ID
GWAS Study Type
6260 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LS
Lutz SM
CM
Cho MH
YK
Young K
HC
Hersh CP
CP
Castaldi PJ
MM
McDonald ML
RE
Regan E
MM
Mattheisen M
DD
DeMeo DL
PM
Parker M
FM
Foreman M
MB
Make BJ
JR
Jensen RL
CR
Casaburi R
LD
Lomas DA
BS
Bhatt SP
BP
Bakke P
GA
Gulsvik A
CJ
Crapo JD
BT
Beaty TH
LN
Laird NM
LC
Lange C
HJ
Hokanson JE
SE
Silverman EK
Chapter II

Abstract

Summary of the research findings

Pulmonary function decline is a major contributor to morbidity and mortality among smokers. Post bronchodilator FEV1 and FEV1/FVC ratio are considered the standard assessment of airflow obstruction. We performed a genome-wide association study (GWAS) in 9919 current and former smokers in the COPDGene study (6659 non-Hispanic Whites [NHW] and 3260 African Americans [AA]) to identify associations with spirometric measures (post-bronchodilator FEV1 and FEV1/FVC). We also conducted meta-analysis of FEV1 and FEV1/FVC GWAS in the COPDGene, ECLIPSE, and GenKOLS cohorts (total n = 13,532).

5,439 European ancestry current and former smoker cases, 821 African American current and former smoker cases

Chapter III

Study Statistics

Key metrics and study information

6260
Total Participants
GWAS
Study Type
No
Replicated
European, African American or Afro-Caribbean
Ancestry
U.S., Norway
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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