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GWAS Study

Association of genetic variants for plasma LRG1 with rapid decline in kidney function in patients with type 2 diabetes.

Gurung RL, Dorajoo R, M Y et al.

33889958 PubMed ID
GWAS Study Type
3694 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GR
Gurung RL
DR
Dorajoo R
MY
M Y
LJ
Liu JJ
PS
Pek SLT
WJ
Wang J
WL
Wang L
SX
Sim X
LS
Liu S
SY
Shao YM
AK
Ang K
ST
Subramaniam T
TW
Tang WE
SC
Sum CF
LJ
Liu JJ
LS
Lim SC
Chapter II

Abstract

Summary of the research findings

Context: Elevated levels of plasma leucine-rich α-2-glycoprotein 1 (LRG1), a component of transforming growth factor beta signaling, are associated with development and progression of chronic kidney disease in patients with type 2 diabetes (T2D). However, whether this relationship is causal is uncertain.

983 Chinese ancestry individuals, 420 Malay ancestry individuals, 478 Indian ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

3694
Total Participants
GWAS
Study Type
Yes
Replicated
1,813 Chinese ancestry individuals
Replication Participants
South Asian, East Asian, South East Asian
Ancestry
Singapore
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.