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Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.

Publication ,  Journal Article
Li, Y-J; Goh, L; Khor, C-C; Fan, Q; Yu, M; Han, S; Sim, X; Ong, RT-H; Wong, T-Y; Vithana, EN; Yap, E; Nakanishi, H; Matsuda, F; Yoshimura, N ...
Published in: Ophthalmology
February 2011

OBJECTIVE: To determine susceptibility genes for high myopia in Singaporean Chinese. DESIGN: A meta-analysis of 2 genome-wide association (GWA) datasets in Chinese and a follow-up replication cohort in Japanese. PARTICIPANTS AND CONTROLS: Two independent datasets of Singaporean Chinese individuals aged 10 to 12 years (Singapore Cohort Study of the Risk factors for Myopia [SCORM]: cases = 65, controls = 238) and more than 21 years (Singapore Prospective Study Program [SP2]: cases = 222, controls = 435) for GWA studies, and a Japanese dataset aged more than 20 years (cases = 959, controls = 2128) for replication. METHODS: Genomic DNA samples from SCORM and SP2 were genotyped using various Illumina Beadarray platforms (>HumanHap 500). Single-locus association tests were conducted for each dataset with meta-analysis using pooled z-scores. The top-ranked genetic markers were examined for replication in the Japanese dataset. Fisher P was calculated for the combined analysis of all 3 cohorts. MAIN OUTCOME MEASURES: High myopia, defined by spherical equivalent (SE) ≤ -6.00 diopters (D); controls defined by SE between -0.50 and +1.00 D. RESULTS: Two SNPs (rs12716080 and rs6885224) in the gene CTNND2 on chromosome 5p15 ranked top in the meta-analysis of our Chinese datasets (meta P = 1.14 × 10(-5) and meta P = 1.51 × 10(-5), respectively) with strong supporting evidence in each individual dataset analysis (max P = 1.85 × 10(-4) in SCORM: max P = 8.8 × 10(-3) in SP2). Evidence of replication was observed in the Japanese dataset for rs6885224 (P = 0.035, meta P of 3 datasets: 7.84 × 10(-6)). CONCLUSIONS: This study identified a strong association of CTNND2 for high myopia in Asian datasets. The CTNND2 gene maps to a known high myopia linkage region on chromosome 5p15.

Duke Scholars

Published In

Ophthalmology

DOI

EISSN

1549-4713

Publication Date

February 2011

Volume

118

Issue

2

Start / End Page

368 / 375

Location

United States

Related Subject Headings

  • Singapore
  • Risk Factors
  • Prospective Studies
  • Polymorphism, Single Nucleotide
  • Phenotype
  • Ophthalmology & Optometry
  • Myopia, Degenerative
  • Middle Aged
  • Meta-Analysis as Topic
  • Male
 

Citation

APA
Chicago
ICMJE
MLA
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Li, Y.-J., Goh, L., Khor, C.-C., Fan, Q., Yu, M., Han, S., … Saw, S.-M. (2011). Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese. Ophthalmology, 118(2), 368–375. https://doi.org/10.1016/j.ophtha.2010.06.016
Li, Yi-Ju, Liang Goh, Chiea-Chuen Khor, Qiao Fan, Miao Yu, Siyu Han, Xueling Sim, et al. “Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.Ophthalmology 118, no. 2 (February 2011): 368–75. https://doi.org/10.1016/j.ophtha.2010.06.016.
Li Y-J, Goh L, Khor C-C, Fan Q, Yu M, Han S, et al. Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese. Ophthalmology. 2011 Feb;118(2):368–75.
Li, Yi-Ju, et al. “Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.Ophthalmology, vol. 118, no. 2, Feb. 2011, pp. 368–75. Pubmed, doi:10.1016/j.ophtha.2010.06.016.
Li Y-J, Goh L, Khor C-C, Fan Q, Yu M, Han S, Sim X, Ong RT-H, Wong T-Y, Vithana EN, Yap E, Nakanishi H, Matsuda F, Ohno-Matsui K, Yoshimura N, Seielstad M, Tai E-S, Young TL, Saw S-M. Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese. Ophthalmology. 2011 Feb;118(2):368–375.
Journal cover image

Published In

Ophthalmology

DOI

EISSN

1549-4713

Publication Date

February 2011

Volume

118

Issue

2

Start / End Page

368 / 375

Location

United States

Related Subject Headings

  • Singapore
  • Risk Factors
  • Prospective Studies
  • Polymorphism, Single Nucleotide
  • Phenotype
  • Ophthalmology & Optometry
  • Myopia, Degenerative
  • Middle Aged
  • Meta-Analysis as Topic
  • Male