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GWAS Study

Novel locus including FGF21 is associated with dietary macronutrient intake.

Chu AY, Workalemahu T, Paynter NP et al.

23372041 PubMed ID
GWAS Study Type
71893 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CA
Chu AY
WT
Workalemahu T
PN
Paynter NP
RL
Rose LM
GF
Giulianini F
TT
Tanaka T
NJ
Ngwa JS
QQ
Qi Q
CG
Curhan GC
RE
Rimm EB
HD
Hunter DJ
PL
Pasquale LR
RP
Ridker PM
HF
Hu FB
CD
Chasman DI
QL
Qi L
Chapter II

Abstract

Summary of the research findings

Dietary intake of macronutrients (carbohydrate, protein, and fat) has been associated with risk of chronic conditions such as obesity and diabetes. Family studies have reported a moderate contribution of genetics to variation in macronutrient intake. In a genome-wide meta-analysis of a population-based discovery cohort (n = 33 533), rs838133 in FGF21 (19q13.33), rs197273 near TRAF family member-associated NF-kappa-B activator (TANK) (2p24.2), and rs10163409 in FTO (16q12.2) were among the top associations (P < 10(-5)) for percentage of total caloric intake from protein and carbohydrate. rs838133 was replicated in silico in an independent sample from the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE) Nutrition Working Group (n = 38 360) and attained genome-wide significance in combined analysis (Pjoint = 7.9 × 10(-9)). A cytokine involved in cellular metabolism, FGF21 is a potential susceptibility gene for obesity and type 2 diabetes. Our results highlight the potential of genetic variation for determining dietary macronutrient intake.

33,533 European ancestry individuuals

Chapter III

Study Statistics

Key metrics and study information

71893
Total Participants
GWAS
Study Type
Yes
Replicated
38,360 European ancestry individuuals
Replication Participants
European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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