Menu
GWAS Study

Defining the genetic control of human blood plasma N-glycome using genome-wide association study.

Sharapov SZ, Tsepilov YA, Klaric L et al.

31163085 PubMed ID
GWAS Study Type
3975 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SS
Sharapov SZ
TY
Tsepilov YA
KL
Klaric L
MM
Mangino M
TG
Thareja G
SA
Shadrina AS
SM
Simurina M
DC
Dagostino C
DJ
Dmitrieva J
VM
Vilaj M
VF
Vuckovic F
PT
Pavic T
SJ
Stambuk J
TI
Trbojevic-Akmacic I
KJ
Kristic J
SJ
Simunovic J
MA
Momcilovic A
CH
Campbell H
DM
Doherty M
DM
Dunlop MG
FS
Farrington SM
PM
Pucic-Bakovic M
GC
Gieger C
AM
Allegri M
LE
Louis E
GM
Georges M
SK
Suhre K
ST
Spector T
WF
Williams FMK
LG
Lauc G
AY
Aulchenko YS
Chapter II

Abstract

Summary of the research findings

Glycosylation is a common post-translational modification of proteins. Glycosylation is associated with a number of human diseases. Defining genetic factors altering glycosylation may provide a basis for novel approaches to diagnostic and pharmaceutical applications. Here we report a genome-wide association study of the human blood plasma N-glycome composition in up to 3811 people measured by Ultra Performance Liquid Chromatography (UPLC) technology. Starting with the 36 original traits measured by UPLC, we computed an additional 77 derived traits leading to a total of 113 glycan traits. We studied associations between these traits and genetic polymorphisms located on human autosomes. We discovered and replicated 12 loci. This allowed us to demonstrate an overlap in genetic control between total plasma protein and IgG glycosylation. The majority of revealed loci contained genes that encode enzymes directly involved in glycosylation (FUT3/FUT6, FUT8, B3GAT1, ST6GAL1, B4GALT1, ST3GAL4, MGAT3 and MGAT5) and a known regulator of plasma protein fucosylation (HNF1A). However, we also found loci that could possibly reflect other more complex aspects of glycosylation process. Functional genomic annotation suggested the role of several genes including DERL3, CHCHD10, TMEM121, IGH and IKZF1. The hypotheses we generated may serve as a starting point for further functional studies in this research area.

2,763 individuals

Chapter III

Study Statistics

Key metrics and study information

3975
Total Participants
GWAS
Study Type
Yes
Replicated
327 Arab, South Asian and Filipino ancestry individuals, 294 European ancestry individuals, 591 individuals.
Replication Participants
South Asian, Greater Middle Eastern (Middle Eastern, North African or Persian), NR, European
Ancestry
U.K., Qatar, Italy
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.