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GWAS Study

Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.

Gudmundsson J, Sulem P, Steinthorsdottir V et al.

17603485 PubMed ID
GWAS Study Type
17841 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GJ
Gudmundsson J
SP
Sulem P
SV
Steinthorsdottir V
BJ
Bergthorsson JT
TG
Thorleifsson G
MA
Manolescu A
RT
Rafnar T
GD
Gudbjartsson D
AB
Agnarsson BA
BA
Baker A
SA
Sigurdsson A
BK
Benediktsdottir KR
JM
Jakobsdottir M
BT
Blondal T
SS
Stacey SN
HA
Helgason A
GS
Gunnarsdottir S
OA
Olafsdottir A
KK
Kristinsson KT
BB
Birgisdottir B
GS
Ghosh S
TS
Thorlacius S
MD
Magnusdottir D
SG
Stefansdottir G
KK
Kristjansson K
BY
Bagger Y
WR
Wilensky RL
RM
Reilly MP
MA
Morris AD
KC
Kimber CH
AA
Adeyemo A
CY
Chen Y
ZJ
Zhou J
SW
So WY
TP
Tong PC
NM
Ng MC
HT
Hansen T
AG
Andersen G
BK
Borch-Johnsen K
JT
Jorgensen T
TA
Tres A
FF
Fuertes F
RM
Ruiz-Echarri M
AL
Asin L
SB
Saez B
VB
van Boven E
KS
Klaver S
SD
Swinkels DW
AK
Aben KK
GT
Graif T
CJ
Cashy J
SB
Suarez BK
VV
van Vierssen Trip O
FM
Frigge ML
OC
Ober C
HM
Hofker MH
WC
Wijmenga C
CC
Christiansen C
RD
Rader DJ
PC
Palmer CN
RC
Rotimi C
CJ
Chan JC
PO
Pedersen O
SG
Sigurdsson G
BR
Benediktsson R
JE
Jonsson E
EG
Einarsson GV
MJ
Mayordomo JI
CW
Catalona WJ
KL
Kiemeney LA
BR
Barkardottir RB
GJ
Gulcher JR
TU
Thorsteinsdottir U
KA
Kong A
SK
Stefansson K
Chapter II

Abstract

Summary of the research findings

We performed a genome-wide association scan to search for sequence variants conferring risk of prostate cancer using 1,501 Icelandic men with prostate cancer and 11,290 controls. Follow-up studies involving three additional case-control groups replicated an association of two variants on chromosome 17 with the disease. These two variants, 33 Mb apart, fall within a region previously implicated by family-based linkage studies on prostate cancer. The risks conferred by these variants are moderate individually (allele odds ratio of about 1.20), but because they are common, their joint population attributable risk is substantial. One of the variants is in TCF2 (HNF1beta), a gene known to be mutated in individuals with maturity-onset diabetes of the young type 5. Results from eight case-control groups, including one West African and one Chinese, demonstrate that this variant confers protection against type 2 diabetes.

1,501 European ancestry cases, 11,290 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

17841
Total Participants
GWAS
Study Type
Yes
Replicated
1,992 European ancestry cases, 3,058 European ancestry controls
Replication Participants
European
Ancestry
U.S., Netherlands, Spain, Iceland
Recruitment Country
Chapter IV

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