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GWAS Study

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.

Teumer A, Chaker L, Groeneweg S et al.

30367059 PubMed ID
GWAS Study Type
71652 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TA
Teumer A
CL
Chaker L
GS
Groeneweg S
LY
Li Y
DM
Di Munno C
BC
Barbieri C
SU
Schultheiss UT
TM
Traglia M
AT
Ahluwalia TS
AM
Akiyama M
AE
Appel EVR
AD
Arking DE
AA
Arnold A
AA
Astrup A
BM
Beekman M
BJ
Beilby JP
BS
Bekaert S
BE
Boerwinkle E
BS
Brown SJ
DB
De Buyzere M
CP
Campbell PJ
CG
Ceresini G
CC
Cerqueira C
CF
Cucca F
DI
Deary IJ
DJ
Deelen J
EK
Eckardt KU
EA
Ekici AB
EJ
Eriksson JG
FL
Ferrrucci L
FT
Fiers T
FE
Fiorillo E
FI
Ford I
FC
Fox CS
FC
Fuchsberger C
GT
Galesloot TE
GC
Gieger C
GM
Gögele M
DG
De Grandi A
GN
Grarup N
GK
Greiser KH
HK
Haljas K
HT
Hansen T
HS
Harris SE
VH
van Heemst D
DH
den Heijer M
HA
Hicks AA
DH
den Hollander W
HG
Homuth G
HJ
Hui J
IM
Ikram MA
IT
Ittermann T
JR
Jensen RA
JJ
Jing J
JJ
Jukema JW
KE
Kajantie E
KY
Kamatani Y
KE
Kasbohm E
KJ
Kaufman JM
KL
Kiemeney LA
KM
Kloppenburg M
KF
Kronenberg F
KM
Kubo M
LJ
Lahti J
LB
Lapauw B
LS
Li S
LD
Liewald DCM
LE
Lim EM
LA
Linneberg A
MM
Marina M
MD
Mascalzoni D
MK
Matsuda K
MD
Medenwald D
MC
Meisinger C
MI
Meulenbelt I
DM
De Meyer T
MZ
Meyer Zu Schwabedissen HE
MR
Mikolajczyk R
MM
Moed M
NR
Netea-Maier RT
NI
Nolte IM
OY
Okada Y
PM
Pala M
PC
Pattaro C
PO
Pedersen O
PA
Petersmann A
PE
Porcu E
PI
Postmus I
PP
Pramstaller PP
PB
Psaty BM
RY
Ramos YFM
RR
Rawal R
RP
Redmond P
RJ
Richards JB
RE
Rietzschel ER
RF
Rivadeneira F
RG
Roef G
RJ
Rotter JI
SC
Sala CF
SD
Schlessinger D
SE
Selvin E
SP
Slagboom PE
SN
Soranzo N
ST
Sørensen TIA
ST
Spector TD
SJ
Starr JM
SD
Stott DJ
TY
Taes Y
TD
Taliun D
TT
Tanaka T
TB
Thuesen B
TD
Tiller D
TD
Toniolo D
UA
Uitterlinden AG
VW
Visser WE
WJ
Walsh JP
WS
Wilson SG
WB
Wolffenbuttel BHR
YQ
Yang Q
ZH
Zheng HF
CA
Cappola A
PR
Peeters RP
NS
Naitza S
VH
Völzke H
SS
Sanna S
KA
Köttgen A
VT
Visser TJ
MM
Medici M
Chapter II

Abstract

Summary of the research findings

Thyroid dysfunction is an important public health problem, which affects 10% of the general population and increases the risk of cardiovascular morbidity and mortality. Many aspects of thyroid hormone regulation have only partly been elucidated, including its transport, metabolism, and genetic determinants. Here we report a large meta-analysis of genome-wide association studies for thyroid function and dysfunction, testing 8 million genetic variants in up to 72,167 individuals. One-hundred-and-nine independent genetic variants are associated with these traits. A genetic risk score, calculated to assess their combined effects on clinical end points, shows significant associations with increased risk of both overt (Graves' disease) and subclinical thyroid disease, as well as clinical complications. By functional follow-up on selected signals, we identify a novel thyroid hormone transporter (SLC17A4) and a metabolizing enzyme (AADAT). Together, these results provide new knowledge about thyroid hormone physiology and disease, opening new possibilities for therapeutic targets.

49,269 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

71652
Total Participants
GWAS
Study Type
Yes
Replicated
up to 22,383 European ancestry individuals
Replication Participants
European
Ancestry
U.S., Australia, Germany, Netherlands, Republic of Ireland, U.K., Italy
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.