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GWAS Study

Genome-Wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length.

Li C, Stoma S, Lotta LA et al.

32109421 PubMed ID
GWAS Study Type
78592 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LC
Li C
SS
Stoma S
LL
Lotta LA
WS
Warner S
AE
Albrecht E
AA
Allione A
AP
Arp PP
BL
Broer L
BJ
Buxton JL
DS
Da Silva Couto Alves A
DJ
Deelen J
FI
Fedko IO
GS
Gordon SD
JT
Jiang T
KR
Karlsson R
KN
Kerrison N
LT
Loe TK
MM
Mangino M
MY
Milaneschi Y
MB
Miraglio B
PN
Pervjakova N
RA
Russo A
SI
Surakka I
VD
van der Spek A
VJ
Verhoeven JE
AN
Amin N
BM
Beekman M
BA
Blakemore AI
CF
Canzian F
HS
Hamby SE
HJ
Hottenga JJ
JP
Jones PD
JP
Jousilahti P
MR
Mägi R
MS
Medland SE
MG
Montgomery GW
ND
Nyholt DR
PM
Perola M
PK
Pietiläinen KH
SV
Salomaa V
SE
Sillanpää E
SH
Suchiman HE
VH
van Heemst D
WG
Willemsen G
AA
Agudo A
BH
Boeing H
BD
Boomsma DI
CM
Chirlaque MD
FG
Fagherazzi G
FP
Ferrari P
FP
Franks P
GC
Gieger C
EJ
Eriksson JG
GM
Gunter M
HS
Hägg S
HI
Hovatta I
IL
Imaz L
KJ
Kaprio J
KR
Kaaks R
KT
Key T
KV
Krogh V
MN
Martin NG
MO
Melander O
MA
Metspalu A
MC
Moreno C
ON
Onland-Moret NC
NP
Nilsson P
OK
Ong KK
OK
Overvad K
PD
Palli D
PS
Panico S
PN
Pedersen NL
PB
Penninx BWJH
QJ
Quirós JR
JM
Jarvelin MR
RM
Rodríguez-Barranco M
SR
Scott RA
SG
Severi G
SP
Slagboom PE
ST
Spector TD
TA
Tjonneland A
TA
Trichopoulou A
TR
Tumino R
UA
Uitterlinden AG
VD
van der Schouw YT
VD
van Duijn CM
WE
Weiderpass E
DE
Denchi EL
MG
Matullo G
BA
Butterworth AS
DJ
Danesh J
SN
Samani NJ
WN
Wareham NJ
NC
Nelson CP
LC
Langenberg C
CV
Codd V
Chapter II

Abstract

Summary of the research findings

Leukocyte telomere length (LTL) is a heritable biomarker of genomic aging. In this study, we perform a genome-wide meta-analysis of LTL by pooling densely genotyped and imputed association results across large-scale European-descent studies including up to 78,592 individuals. We identify 49 genomic regions at a false dicovery rate (FDR) < 0.05 threshold and prioritize genes at 31, with five highlighting nucleotide metabolism as an important regulator of LTL. We report six genome-wide significant loci in or near SENP7, MOB1B, CARMIL1, PRRC2A, TERF2, and RFWD3, and our results support recently identified PARP1, POT1, ATM, and MPHOSPH6 loci. Phenome-wide analyses in >350,000 UK Biobank participants suggest that genetically shorter telomere length increases the risk of hypothyroidism and decreases the risk of thyroid cancer, lymphoma, and a range of proliferative conditions. Our results replicate previously reported associations with increased risk of coronary artery disease and lower risk for multiple cancer types. Our findings substantially expand current knowledge on genes that regulate LTL and their impact on human health and disease.

78,592 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

78592
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Estonia, Finland, Germany, Greece, Netherlands, Norway, Sweden, U.K., Australia
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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