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GWAS Study

Characterization of the genetic architecture of infant and early childhood body mass index.

Helgeland Ø, Vaudel M, Sole-Navais P et al.

35315439 PubMed ID
GWAS Study Type
28681 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

Helgeland Ø
VM
Vaudel M
SP
Sole-Navais P
FC
Flatley C
JJ
Juodakis J
BJ
Bacelis J
KI
Koløen IL
KG
Knudsen GP
JB
Johansson BB
MP
Magnus P
KT
Kjennerud TR
JP
Juliusson PB
SC
Stoltenberg C
HO
Holmen OL
AO
Andreassen OA
JB
Jacobsson B
NP
Njølstad PR
JS
Johansson S
Chapter II

Abstract

Summary of the research findings

Early childhood obesity is a growing global concern; however, the role of common genetic variation on infant and child weight development is unclear. Here, we identify 46 loci associated with early childhood body mass index at specific ages, matching different child growth phases, and representing four major trajectory patterns. We perform genome-wide association studies across 12 time points from birth to 8 years in 28,681 children and their parents (27,088 mothers and 26,239 fathers) in the Norwegian Mother, Father and Child Cohort Study. Monogenic obesity genes are overrepresented near identified loci, and several complex association signals near LEPR, GLP1R, PCSK1 and KLF14 point towards a major influence for common variation affecting the leptin-melanocortin system in early life, providing a link to putative treatment strategies. We also demonstrate how different polygenic risk scores transition from birth to adult profiles through early child growth. In conclusion, our results offer a fine-grained characterization of a changing genetic landscape sustaining early childhood growth.

28,681 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

28681
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Norway
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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