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GWAS Study

Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium.

Truong T, Lesueur F, Sugier PE et al.

33527407 PubMed ID
GWAS Study Type
7815 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TT
Truong T
LF
Lesueur F
SP
Sugier PE
GJ
Guibon J
XC
Xhaard C
KM
Karimi M
KO
Kulkarni O
LE
Lucotte EA
BD
Bacq-Daian D
BA
Boland-Auge A
MC
Mulot C
LP
Laurent-Puig P
SC
Schvartz C
GA
Guizard AV
RY
Ren Y
AE
Adjadj E
RF
Rachédi F
BF
Borson-Chazot F
OR
Ortiz RM
LJ
Lence-Anta JJ
PC
Pereda CM
CD
Comiskey DF
HH
He H
LS
Liyanarachchi S
DL
de la Chapelle A
ER
Elisei R
GF
Gemignani F
TH
Thomsen H
FA
Forsti A
HA
Herzig AF
LA
Leutenegger AL
RC
Rubino C
OE
Ostroumova E
KA
Kesminiene A
BM
Boutron-Ruault MC
DJ
Deleuze JF
GP
Guénel P
DV
de Vathaire F
Chapter II

Abstract

Summary of the research findings

Incidence of differentiated thyroid carcinoma (DTC) varies considerably between ethnic groups, with particularly high incidence rates in Pacific Islanders. DTC is one of the cancers with the highest familial risk suggesting a major role of genetic risk factors, but only few susceptibility loci were identified so far. In order to assess the contribution of known DTC susceptibility loci and to identify new ones, we conducted a multiethnic genome-wide association study (GWAS) in individuals of European ancestry and of Oceanian ancestry from Pacific Islands. Our study included 1554 cases/1973 controls of European ancestry and 301 cases/348 controls of Oceanian ancestry from seven population-based case-control studies participating to the EPITHYR consortium. All participants were genotyped using the OncoArray-500K Beadchip (Illumina). We confirmed the association with the known DTC susceptibility loci at 2q35, 8p12, 9q22.33 and 14q13.3 in the European ancestry population and suggested two novel signals at 1p31.3 and 16q23.2, which were associated with thyroid-stimulating hormone levels in previous GWAS. We additionally replicated an association with 5p15.33 reported previously in Chinese and European populations. Except at 1p31.3, all associations were in the same direction in the population of Oceanian ancestry. We also observed that the frequencies of risk alleles at 2q35, 5p15.33 and 16q23.2 were significantly higher in Oceanians than in Europeans. However, additional GWAS and epidemiological studies in Oceanian populations are needed to fully understand the highest incidence observed in these populations.

1,554 European ancestry cases, 1,973 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

7815
Total Participants
GWAS
Study Type
Yes
Replicated
2,229 European ancestry cases, 2,059 European ancestry controls
Replication Participants
European, Oceanian
Ancestry
Belarus, France, Cuba, French Polynesia, New Caledonia, U.S., Italy
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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