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GWAS Study

Common variation in GPC5 is associated with acquired nephrotic syndrome.

Okamoto K, Tokunaga K, Doi K et al.

21441931 PubMed ID
GWAS Study Type
7322 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

OK
Okamoto K
TK
Tokunaga K
DK
Doi K
FT
Fujita T
SH
Suzuki H
KT
Katoh T
WT
Watanabe T
NN
Nishida N
MA
Mabuchi A
TA
Takahashi A
KM
Kubo M
MS
Maeda S
NY
Nakamura Y
NE
Noiri E
Chapter II

Abstract

Summary of the research findings

Severe proteinuria is a defining factor of nephrotic syndrome irrespective of the etiology. Investigation of congenital nephrotic syndrome has shown that dysfunction of glomerular epithelial cells (podocytes) plays a crucial role in this disease. Acquired nephrotic syndrome is also assumed to be associated with podocyte injury. Here we identify an association between variants in GPC5, encoding glypican-5, and acquired nephrotic syndrome through a genome-wide association study and replication analysis (P value under a recessive model (P(rec)) = 6.0 × 10(-11), odds ratio = 2.54). We show that GPC5 is expressed in podocytes and that the risk genotype is associated with higher expression. We further show that podocyte-specific knockdown and systemic short interfering RNA injection confers resistance to podocyte injury in mouse models of nephrosis. This study identifies GPC5 as a new susceptibility gene for nephrotic syndrome and implicates GPC5 as a promising therapeutic target for reducing podocyte vulnerability in glomerular disease.

195 Japanese ancestry cases, 1,546 Japanese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

7322
Total Participants
GWAS
Study Type
Yes
Replicated
662 Japanese ancestry cases, 4,919 Japanese ancestry controls
Replication Participants
East Asian
Ancestry
Japan
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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