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GWAS Study

A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus.

Cozen W, Timofeeva MN, Li D et al.

24920014 PubMed ID
GWAS Study Type
14192 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CW
Cozen W
TM
Timofeeva MN
LD
Li D
DA
Diepstra A
HD
Hazelett D
DM
Delahaye-Sourdeix M
EC
Edlund CK
FL
Franke L
RK
Rostgaard K
VD
Van Den Berg DJ
CV
Cortessis VK
SK
Smedby KE
GS
Glaser SL
WH
Westra HJ
RL
Robison LL
MT
Mack TM
GH
Ghesquieres H
HA
Hwang AE
NA
Nieters A
DS
de Sanjose S
LT
Lightfoot T
BN
Becker N
MM
Maynadie M
FL
Foretova L
RE
Roman E
BY
Benavente Y
RK
Rand KA
NB
Nathwani BN
GB
Glimelius B
SA
Staines A
BP
Boffetta P
LB
Link BK
KL
Kiemeney L
AS
Ansell SM
BS
Bhatia S
SL
Strong LC
GP
Galan P
VL
Vatten L
HT
Habermann TM
DE
Duell EJ
LA
Lake A
VR
Veenstra RN
VL
Visser L
LY
Liu Y
UK
Urayama KY
MD
Montgomery D
GV
Gaborieau V
WL
Weiss LM
BG
Byrnes G
LM
Lathrop M
CP
Cocco P
BT
Best T
SA
Skol AD
AH
Adami HO
MM
Melbye M
CJ
Cerhan JR
GA
Gallagher A
TG
Taylor GM
SS
Slager SL
BP
Brennan P
CG
Coetzee GA
CD
Conti DV
OK
Onel K
JR
Jarrett RF
HH
Hjalgrim H
VD
van den Berg A
MJ
McKay JD
Chapter II

Abstract

Summary of the research findings

Recent genome-wide association studies (GWAS) of Hodgkin lymphoma (HL) have identified associations with genetic variation at both HLA and non-HLA loci; however, much of heritable HL susceptibility remains unexplained. Here we perform a meta-analysis of three HL GWAS totaling 1,816 cases and 7,877 controls followed by replication in an independent set of 1,281 cases and 3,218 controls to find novel risk loci. We identify a novel variant at 19p13.3 associated with HL (rs1860661; odds ratio (OR)=0.81, 95% confidence interval (95% CI) = 0.76-0.86, P(combined) = 3.5 × 10(-10)), located in intron 2 of TCF3 (also known as E2A), a regulator of B- and T-cell lineage commitment known to be involved in HL pathogenesis. This meta-analysis also notes associations between previously published loci at 2p16, 5q31, 6p31, 8q24 and 10p14 and HL subtypes. We conclude that our data suggest a link between the 19p13.3 locus, including TCF3, and HL risk.

1,816 European ancestry cases, 7,877 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

14192
Total Participants
GWAS
Study Type
Yes
Replicated
1,281 European ancestry cases, 3,218 European ancestry controls
Replication Participants
European
Ancestry
Sweden, U.S., Czech Republic, Italy, Germany, U.K., Spain, France, Republic of Ireland, Denmark
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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