Menu
GWAS Study

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.

Felix JF, Bradfield JP, Monnereau C et al.

26604143 PubMed ID
GWAS Study Type
46057 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

FJ
Felix JF
BJ
Bradfield JP
MC
Monnereau C
VD
van der Valk RJ
SE
Stergiakouli E
CA
Chesi A
GR
Gaillard R
FB
Feenstra B
TE
Thiering E
KE
Kreiner-Møller E
MA
Mahajan A
PN
Pitkänen N
JR
Joro R
CA
Cavadino A
HV
Huikari V
FS
Franks S
GM
Groen-Blokhuis MM
CD
Cousminer DL
MJ
Marsh JA
LT
Lehtimäki T
CJ
Curtin JA
VJ
Vioque J
AT
Ahluwalia TS
MR
Myhre R
PT
Price TS
VN
Vilor-Tejedor N
YL
Yengo L
GN
Grarup N
NI
Ntalla I
AW
Ang W
AM
Atalay M
BH
Bisgaard H
BA
Blakemore AI
BA
Bonnefond A
CL
Carstensen L
EJ
Eriksson J
FC
Flexeder C
FL
Franke L
GF
Geller F
GM
Geserick M
HA
Hartikainen AL
HC
Haworth CM
HJ
Hirschhorn JN
HA
Hofman A
HJ
Holm JC
HM
Horikoshi M
HJ
Hottenga JJ
HJ
Huang J
KH
Kadarmideen HN
KM
Kähönen M
KW
Kiess W
LH
Lakka HM
LT
Lakka TA
LA
Lewin AM
LL
Liang L
LL
Lyytikäinen LP
MB
Ma B
MP
Magnus P
MS
McCormack SE
MG
McMahon G
MF
Mentch FD
MC
Middeldorp CM
MC
Murray CS
PK
Pahkala K
PT
Pers TH
PR
Pfäffle R
PD
Postma DS
PC
Power C
SA
Simpson A
SV
Sengpiel V
TC
Tiesler CM
TM
Torrent M
UA
Uitterlinden AG
VM
van Meurs JB
VR
Vinding R
WJ
Waage J
WJ
Wardle J
ZE
Zeggini E
ZB
Zemel BS
DG
Dedoussis GV
PO
Pedersen O
FP
Froguel P
SJ
Sunyer J
PR
Plomin R
JB
Jacobsson B
HT
Hansen T
GJ
Gonzalez JR
CA
Custovic A
RO
Raitakari OT
PC
Pennell CE
WE
Widén E
BD
Boomsma DI
KG
Koppelman GH
SS
Sebert S
JM
Järvelin MR
HE
Hyppönen E
MM
McCarthy MI
LV
Lindi V
HN
Harri N
KA
Körner A
BK
Bønnelykke K
HJ
Heinrich J
MM
Melbye M
RF
Rivadeneira F
HH
Hakonarson H
RS
Ring SM
SG
Smith GD
ST
Sørensen TI
TN
Timpson NJ
GS
Grant SF
JV
Jaddoe VW
Chapter II

Abstract

Summary of the research findings

A large number of genetic loci are associated with adult body mass index. However, the genetics of childhood body mass index are largely unknown. We performed a meta-analysis of genome-wide association studies of childhood body mass index, using sex- and age-adjusted standard deviation scores. We included 35 668 children from 20 studies in the discovery phase and 11 873 children from 13 studies in the replication phase. In total, 15 loci reached genome-wide significance (P-value < 5 × 10(-8)) in the joint discovery and replication analysis, of which 12 are previously identified loci in or close to ADCY3, GNPDA2, TMEM18, SEC16B, FAIM2, FTO, TFAP2B, TNNI3K, MC4R, GPR61, LMX1B and OLFM4 associated with adult body mass index or childhood obesity. We identified three novel loci: rs13253111 near ELP3, rs8092503 near RAB27B and rs13387838 near ADAM23. Per additional risk allele, body mass index increased 0.04 Standard Deviation Score (SDS) [Standard Error (SE) 0.007], 0.05 SDS (SE 0.008) and 0.14 SDS (SE 0.025), for rs13253111, rs8092503 and rs13387838, respectively. A genetic risk score combining all 15 SNPs showed that each additional average risk allele was associated with a 0.073 SDS (SE 0.011, P-value = 3.12 × 10(-10)) increase in childhood body mass index in a population of 1955 children. This risk score explained 2% of the variance in childhood body mass index. This study highlights the shared genetic background between childhood and adult body mass index and adds three novel loci. These loci likely represent age-related differences in strength of the associations with body mass index.

34,744 European ancestry children

Chapter III

Study Statistics

Key metrics and study information

46057
Total Participants
GWAS
Study Type
Yes
Replicated
11,313 European ancestry children
Replication Participants
European
Ancestry
Finland, U.S., Netherlands, Greece, Germany, U.K., Spain, France, Denmark, Australia
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.