Menu
GWAS Study

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants.

Young KL, Fisher V, Deng X et al.

36568030 PubMed ID
GWAS Study Type
11249 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

YK
Young KL
FV
Fisher V
DX
Deng X
BJ
Brody JA
GM
Graff M
LE
Lim E
LB
Lin BM
XH
Xu H
AN
Amin N
AP
An P
AS
Aslibekyan S
FA
Fohner AE
HB
Hidalgo B
LP
Lenzini P
KR
Kraaij R
MC
Medina-Gomez C
PI
Prokić I
RF
Rivadeneira F
SC
Sitlani C
TR
Tao R
VR
van Rooij J
ZD
Zhang D
BJ
Broome JG
BE
Buth EJ
HB
Heavner BD
JD
Jain D
SA
Smith AV
BK
Barnes K
BM
Boorgula MP
CS
Chavan S
DD
Darbar D
DA
De Andrade M
GX
Guo X
HJ
Haessler J
IM
Irvin MR
KR
Kalyani RR
KS
Kardia SLR
KC
Kooperberg C
KW
Kim W
MR
Mathias RA
MM
McDonald ML
MB
Mitchell BD
PP
Peyser PA
RE
Regan EA
RS
Redline S
RA
Reiner AP
RS
Rich SS
RJ
Rotter JI
SJ
Smith JA
WS
Weiss S
WK
Wiggins KL
YL
Yanek LR
AD
Arnett D
HN
Heard-Costa NL
LS
Leal S
LD
Lin D
MB
McKnight B
PM
Province M
VD
van Duijn CM
NK
North KE
CL
Cupples LA
LC
Liu CT
Chapter II

Abstract

Summary of the research findings

Anthropometric traits, measuring body size and shape, are highly heritable and significant clinical risk factors for cardiometabolic disorders. These traits have been extensively studied in genome-wide association studies (GWASs), with hundreds of genome-wide significant loci identified. We performed a whole-exome sequence analysis of the genetics of height, body mass index (BMI) and waist/hip ratio (WHR). We meta-analyzed single-variant and gene-based associations of whole-exome sequence variation with height, BMI, and WHR in up to 22,004 individuals, and we assessed replication of our findings in up to 16,418 individuals from 10 independent cohorts from Trans-Omics for Precision Medicine (TOPMed). We identified four trait associations with single-nucleotide variants (SNVs; two for height and two for BMI) and replicated the LECT2 gene association with height. Our expression quantitative trait locus (eQTL) analysis within previously reported GWAS loci implicated CEP63 and RFT1 as potential functional genes for known height loci. We further assessed enrichment of SNVs, which were monogenic or syndromic variants within loci associated with our three traits. This led to the significant enrichment results for height, whereas we observed no Bonferroni-corrected significance for all SNVs. With a sample size of ∼20,000 whole-exome sequences in our discovery dataset, our findings demonstrate the importance of genomic sequencing in genetic association studies, yet they also illustrate the challenges in identifying effects of rare genetic variants.

4,605 African ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

11249
Total Participants
GWAS
Study Type
Yes
Replicated
6,644 African American individuals
Replication Participants
African unspecified, African American or Afro-Caribbean, European
Ancestry
U.S., Netherlands
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.