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GWAS Study

Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits.

Westerman KE, Walker ME, Gaynor SM et al.

36791419 PubMed ID
GWAS Study Type
29783 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WK
Westerman KE
WM
Walker ME
GS
Gaynor SM
WJ
Wessel J
DD
DiCorpo D
MJ
Ma J
AA
Alonso A
AS
Aslibekyan S
BA
Baldridge AS
BA
Bertoni AG
BM
Biggs ML
BJ
Brody JA
CY
Chen YI
DJ
Dupuis J
GM
Goodarzi MO
GX
Guo X
HN
Hasbani NR
HA
Heath A
HB
Hidalgo B
IM
Irvin MR
JW
Johnson WC
KR
Kalyani RR
LL
Lange L
LR
Lemaitre RN
LC
Liu CT
LS
Liu S
MJ
Moon JY
NR
Nassir R
PJ
Pankow JS
PM
Pettinger M
RL
Raffield LM
RL
Rasmussen-Torvik LJ
SE
Selvin E
SM
Senn MK
SA
Shadyab AH
SA
Smith AV
SN
Smith NL
SL
Steffen L
TS
Talegakwar S
TK
Taylor KD
DV
de Vries PS
WJ
Wilson JG
WA
Wood AC
YL
Yanek LR
YJ
Yao J
ZY
Zheng Y
BE
Boerwinkle E
MA
Morrison AC
FM
Fornage M
RT
Russell TP
PB
Psaty BM
LD
Levy D
HN
Heard-Costa NL
RV
Ramachandran VS
MR
Mathias RA
AD
Arnett DK
KR
Kaplan R
NK
North KE
CA
Correa A
CA
Carson A
RJ
Rotter JI
RS
Rich SS
MJ
Manson JE
RA
Reiner AP
KC
Kooperberg C
FJ
Florez JC
MJ
Meigs JB
MJ
Merino J
TD
Tobias DK
CH
Chen H
MA
Manning AK
Chapter II

Abstract

Summary of the research findings

Few studies have demonstrated reproducible gene-diet interactions (GDIs) impacting metabolic disease risk factors, likely due in part to measurement error in dietary intake estimation and insufficient capture of rare genetic variation. We aimed to identify GDIs across the genetic frequency spectrum impacting the macronutrient-glycemia relationship in genetically and culturally diverse cohorts. We analyzed 33,187 participants free of diabetes from 10 National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine program cohorts with whole-genome sequencing, self-reported diet, and glycemic trait data. We fit cohort-specific, multivariable-adjusted linear mixed models for the effect of diet, modeled as an isocaloric substitution of carbohydrate for fat, and its interactions with common and rare variants genome-wide. In main effect meta-analyses, participants consuming more carbohydrate had modestly lower glycemic trait values (e.g., for glycated hemoglobin [HbA1c], -0.013% HbA1c/250 kcal substitution). In GDI meta-analyses, a common African ancestry-enriched variant (rs79762542) reached study-wide significance and replicated in the UK Biobank cohort, indicating a negative carbohydrate-HbA1c association among major allele homozygotes only. Simulations revealed that >150,000 samples may be necessary to identify similar macronutrient GDIs under realistic assumptions about effect size and measurement error. These results generate hypotheses for further exploration of modifiable metabolic disease risk in additional cohorts with African ancestry.

4,328 African American individuals, 35 American Indian ancestry individuals, 122 Asian ancestry individuals, 18,214 European ancestry individuals, 7,084 Hispanic or Latin American individuals

Chapter III

Study Statistics

Key metrics and study information

29783
Total Participants
GWAS
Study Type
No
Replicated
African American or Afro-Caribbean, Native American, Asian unspecified, European, Hispanic or Latin American
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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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.