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GWAS Study

Genome-wide association study identified novel loci and gene-environment interaction for refractive error in children.

Wang Y, Zhang Y, Chen H et al.

40410244 PubMed ID
GWAS Study Type
5330 Participants
92 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WY
Wang Y
ZY
Zhang Y
CH
Chen H
ZX
Zhang XJ
ZR
Zhang R
NT
Ng TK
TJ
Tham JA
KK
Kam KW
TP
Tam POS
YA
Young AL
WY
Wei Y
ZM
Zhang M
PC
Pang CP
TC
Tham CC
YJ
Yam JC
CL
Chen LJ
Chapter II

Abstract

Summary of the research findings

To identify novel genetic loci for children refractive error, we performed a meta-analysis of two genome-wide association studies (GWASs) of spherical equivalent (SE) in 1,237 children from the population-based Hong Kong Children Eye Study (HKCES) and the Low Concentration Atropine for Myopia Progression (LAMP) study. Replication was conducted in 4,093 Chinese children and 1,814 Chinese adults. Four lead-SNPs (MIR4275 rs292034, TENM3 rs17074027, LOC101928911 rs6925312 and FAM135B rs4609227) showed genome-wide significant association (P ≤ 5.0 × 10-8) with SE. TENM3 had been associated with myopia in adults before, whilst the other three loci, MIR4275, LOC101928911 and FAM135B, were novel. Significant interaction between genetic risk scores (GRS) and near work on SE was also detected (βinteraction = 0.14, Pinteraction = 0.0003). This study identified novel genetic loci for children refractive error and suggested myopia intervention can be individualized based on the genetic risk of children.

1,237 Southern Han Chinese ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

5330
Total Participants
GWAS
Study Type
Yes
Replicated
4,093 East Asian ancestry individuals
Replication Participants
East Asian
Ancestry
China, Hong Kong SAR
Recruitment Country
Chapter IV

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