Menu
Currency
GWAS Study

Assessing the causal association of glycine with risk of cardio-metabolic diseases.

Wittemans LBL, Lotta LA, Oliver-Williams C et al.

30837465 PubMed ID
GWAS Study Type
80003 Participants
45 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WL
Wittemans LBL
LL
Lotta LA
OC
Oliver-Williams C
SI
Stewart ID
SP
Surendran P
KS
Karthikeyan S
DF
Day FR
KA
Koulman A
IF
Imamura F
ZL
Zeng L
EJ
Erdmann J
SH
Schunkert H
KK
Khaw KT
GJ
Griffin JL
FN
Forouhi NG
SR
Scott RA
WA
Wood AM
BS
Burgess S
HJ
Howson JMM
DJ
Danesh J
WN
Wareham NJ
BA
Butterworth AS
LC
Langenberg C
Chapter II

Abstract

Summary of the research findings

Circulating levels of glycine have previously been associated with lower incidence of coronary heart disease (CHD) and type 2 diabetes (T2D) but it remains uncertain if glycine plays an aetiological role. We present a meta-analysis of genome-wide association studies for glycine in 80,003 participants and investigate the causality and potential mechanisms of the association between glycine and cardio-metabolic diseases using genetic approaches. We identify 27 genetic loci, of which 22 have not previously been reported for glycine. We show that glycine is genetically associated with lower CHD risk and find that this may be partly driven by blood pressure. Evidence for a genetic association of glycine with T2D is weaker, but we find a strong inverse genetic effect of hyperinsulinaemia on glycine. Our findings strengthen evidence for a protective effect of glycine on CHD and show that the glycine-T2D association may be driven by a glycine-lowering effect of insulin resistance.

80,003 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

80003
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Finland, U.K.
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.