TY - JOUR
T1 - Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits
AU - Vogelezang, Suzanne
AU - Bradfield, Jonathan P
AU - Ahluwalia, Tarun S
AU - Curtin, John A
AU - Lakka, Timo A.
AU - Grarup, Niels
AU - Scholz, Markus
AU - van der Most, Peter J.
AU - Monnereau, Claire
AU - Stergiakouli, Evie
AU - Heiskala, Anni
AU - Horikoshi, Momoko
AU - Fedko, Iryna O.
AU - Vilor-Tejedor, Natalia
AU - Cousminer, Diana L.
AU - Standl, Marie
AU - Wang, Carol A.
AU - Viikari, Jorma
AU - Geller, Frank
AU - Íñiguez, Carmen
AU - Pitkänen, Niina
AU - Chesi, Alessandra
AU - Bacelis, Jonas
AU - Yengo, Loic
AU - Torrent, Maties
AU - Ntalla, Ioanna
AU - Helgeland, Øyvind
AU - Selzam, Saskia
AU - Vonk, Judith M.
AU - Zafarmand, Mohammed H.
AU - Heude, Barbara
AU - Farooqi, Ismaa Sadaf
AU - Alyass, Akram
AU - Have, Christian T.
AU - Schnurr, Theresia Maria
AU - Bønnelykke, Klaus
AU - Carstensen, Lisbeth
AU - Chawes, Bo
AU - Hansen, Torben
AU - Hollensted, Mette
AU - Melbye, Mads
AU - Michaelsen, Kim F.
AU - Morgen, Camilla Schmidt
AU - Pedersen, Oluf Borbye
AU - Stokholm, Jakob
AU - Lind, Mads Vendelbo
AU - Frithioff-Bøjsøe, Christine
AU - Nohr, Ellen A.
AU - Sørensen, Thorkild I.A.
AU - Holm, Jens-Christian
AU - Bisgaard, Hans
AU - Felix, Janine F
AU - Early Growth Genetics Consortium
N1 - CURIS 2020 NEXS 336
PY - 2020
Y1 - 2020
N2 - The genetic background of childhood body mass index (BMI), and the extent to which the well-known associations of childhood BMI with adult diseases are explained by shared genetic factors, are largely unknown. We performed a genome-wide association study meta-analysis of BMI in 61,111 children aged between 2 and 10 years. Twenty-five independent loci reached genome-wide significance in the combined discovery and replication analyses. Two of these, located near NEDD4L and SLC45A3, have not previously been reported in relation to either childhood or adult BMI. Positive genetic correlations of childhood BMI with birth weight and adult BMI, waist-to-hip ratio, diastolic blood pressure and type 2 diabetes were detected (Rg ranging from 0.11 to 0.76, P-values <0.002). A negative genetic correlation of childhood BMI with age at menarche was observed. Our results suggest that the biological processes underlying childhood BMI largely, but not completely, overlap with those underlying adult BMI. The well-known observational associations of BMI in childhood with cardio-metabolic diseases in adulthood may reflect partial genetic overlap, but in light of previous evidence, it is also likely that they are explained through phenotypic continuity of BMI from childhood into adulthood.
AB - The genetic background of childhood body mass index (BMI), and the extent to which the well-known associations of childhood BMI with adult diseases are explained by shared genetic factors, are largely unknown. We performed a genome-wide association study meta-analysis of BMI in 61,111 children aged between 2 and 10 years. Twenty-five independent loci reached genome-wide significance in the combined discovery and replication analyses. Two of these, located near NEDD4L and SLC45A3, have not previously been reported in relation to either childhood or adult BMI. Positive genetic correlations of childhood BMI with birth weight and adult BMI, waist-to-hip ratio, diastolic blood pressure and type 2 diabetes were detected (Rg ranging from 0.11 to 0.76, P-values <0.002). A negative genetic correlation of childhood BMI with age at menarche was observed. Our results suggest that the biological processes underlying childhood BMI largely, but not completely, overlap with those underlying adult BMI. The well-known observational associations of BMI in childhood with cardio-metabolic diseases in adulthood may reflect partial genetic overlap, but in light of previous evidence, it is also likely that they are explained through phenotypic continuity of BMI from childhood into adulthood.
UR - http://www.scopus.com/inward/record.url?scp=85092931223&partnerID=8YFLogxK
U2 - 10.1371/journal.pgen.1008718
DO - 10.1371/journal.pgen.1008718
M3 - Journal article
C2 - 33045005
AN - SCOPUS:85092931223
VL - 16
JO - P L o S Genetics
JF - P L o S Genetics
SN - 1553-7390
IS - 10
M1 - e1008718
ER -