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GWAS Study

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.

Erzurumluoglu AM, Liu M, Jackson VE et al.

30617275 PubMed ID
GWAS Study Type
622409 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

EA
Erzurumluoglu AM
LM
Liu M
JV
Jackson VE
BD
Barnes DR
DG
Datta G
MC
Melbourne CA
YR
Young R
BC
Batini C
SP
Surendran P
JT
Jiang T
AS
Adnan SD
AS
Afaq S
AA
Agrawal A
AE
Altmaier E
AA
Antoniou AC
AF
Asselbergs FW
BC
Baumbach C
BL
Bierut L
BS
Bertelsen S
BM
Boehnke M
BM
Bots ML
BD
Brazel DM
CJ
Chambers JC
CJ
Chang-Claude J
CC
Chen C
CJ
Corley J
CY
Chou YL
DS
David SP
DB
de Boer RA
DL
de Leeuw CA
DJ
Dennis JG
DA
Dominiczak AF
DA
Dunning AM
ED
Easton DF
EC
Eaton C
EP
Elliott P
EE
Evangelou E
FJ
Faul JD
FT
Foroud T
GA
Goate A
GJ
Gong J
GH
Grabe HJ
HJ
Haessler J
HC
Haiman C
HG
Hallmans G
HA
Hammerschlag AR
HS
Harris SE
HA
Hattersley A
HA
Heath A
HC
Hsu C
IW
Iacono WG
KS
Kanoni S
KM
Kapoor M
KJ
Kaprio J
KS
Kardia SL
KF
Karpe F
KJ
Kontto J
KJ
Kooner JS
KC
Kooperberg C
KK
Kuulasmaa K
LM
Laakso M
LD
Lai D
LC
Langenberg C
LN
Le N
LG
Lettre G
LA
Loukola A
LJ
Luan J
MP
Madden PAF
MM
Mangino M
MR
Marioni RE
ME
Marouli E
MJ
Marten J
MN
Martin NG
MM
McGue M
MK
Michailidou K
ME
Mihailov E
MA
Moayyeri A
MM
Moitry M
MM
Müller-Nurasyid M
NA
Naheed A
NM
Nauck M
NM
Neville MJ
NS
Nielsen SF
NK
North K
PM
Perola M
PP
Pharoah PDP
PG
Pistis G
PT
Polderman TJ
PD
Posthuma D
PN
Poulter N
QB
Qaiser B
RA
Rasheed A
RA
Reiner A
RF
Renström F
RJ
Rice J
RR
Rohde R
RO
Rolandsson O
SN
Samani NJ
SM
Samuel M
SD
Schlessinger D
SS
Scholte SH
SR
Scott RA
SP
Sever P
SY
Shao Y
SN
Shrine N
SJ
Smith JA
SJ
Starr JM
SK
Stirrups K
SD
Stram D
SH
Stringham HM
TI
Tachmazidou I
TJ
Tardif JC
TD
Thompson DJ
TH
Tindle HA
TV
Tragante V
TS
Trompet S
TV
Turcot V
TJ
Tyrrell J
VI
Vaartjes I
VD
van der Leij AR
VD
van der Meer P
VT
Varga TV
VN
Verweij N
VH
Völzke H
WN
Wareham NJ
WH
Warren HR
WD
Weir DR
WS
Weiss S
WL
Wetherill L
YH
Yaghootkar H
YE
Yavas E
JY
Jiang Y
CF
Chen F
ZX
Zhan X
ZW
Zhang W
ZW
Zhao W
ZW
Zhao W
ZK
Zhou K
AP
Amouyel P
BS
Blankenberg S
CM
Caulfield MJ
CR
Chowdhury R
CF
Cucca F
DI
Deary IJ
DP
Deloukas P
DA
Di Angelantonio E
FM
Ferrario M
FJ
Ferrières J
FP
Franks PW
FT
Frayling TM
FP
Frossard P
HI
Hall IP
HC
Hayward C
JJ
Jansson JH
JJ
Jukema JW
KF
Kee F
MS
Männistö S
MA
Metspalu A
MP
Munroe PB
NB
Nordestgaard BG
PC
Palmer CNA
SV
Salomaa V
SN
Sattar N
ST
Spector T
SD
Strachan DP
VD
van der Harst P
ZE
Zeggini E
SD
Saleheen D
BA
Butterworth AS
WL
Wain LV
AG
Abecasis GR
DJ
Danesh J
TM
Tobin MD
VS
Vrieze S
LD
Liu DJ
HJ
Howson JMM
Chapter II

Abstract

Summary of the research findings

Smoking is a major heritable and modifiable risk factor for many diseases, including cancer, common respiratory disorders and cardiovascular diseases. Fourteen genetic loci have previously been associated with smoking behaviour-related traits. We tested up to 235,116 single nucleotide variants (SNVs) on the exome-array for association with smoking initiation, cigarettes per day, pack-years, and smoking cessation in a fixed effects meta-analysis of up to 61 studies (up to 346,813 participants). In a subset of 112,811 participants, a further one million SNVs were also genotyped and tested for association with the four smoking behaviour traits. SNV-trait associations with P < 5 × 10-8 in either analysis were taken forward for replication in up to 275,596 independent participants from UK Biobank. Lastly, a meta-analysis of the discovery and replication studies was performed. Sixteen SNVs were associated with at least one of the smoking behaviour traits (P < 5 × 10-8) in the discovery samples. Ten novel SNVs, including rs12616219 near TMEM182, were followed-up and five of them (rs462779 in REV3L, rs12780116 in CNNM2, rs1190736 in GPR101, rs11539157 in PJA1, and rs12616219 near TMEM182) replicated at a Bonferroni significance threshold (P < 4.5 × 10-3) with consistent direction of effect. A further 35 SNVs were associated with smoking behaviour traits in the discovery plus replication meta-analysis (up to 622,409 participants) including a rare SNV, rs150493199, in CCDC141 and two low-frequency SNVs in CEP350 and HDGFRP2. Functional follow-up implied that decreased expression of REV3L may lower the probability of smoking initiation. The novel loci will facilitate understanding the genetic aetiology of smoking behaviour and may lead to the identification of potential drug targets for smoking prevention and/or cessation.

324,851 European ancestry individuals, 21,962 South Asian ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

622409
Total Participants
GWAS
Study Type
Yes
Replicated
up to 275,596 European ancestry individuals
Replication Participants
South Asian, European
Ancestry
Bangladesh, Pakistan, U.K., Canada, U.S., Australia, France, Germany, Netherlands, Denmark, Estonia, Finland, Norway, Sweden, Croatia, Italy, Spain
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.