A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1

PLoS Genet. 2009 Sep;5(9):e1000660. doi: 10.1371/journal.pgen.1000660. Epub 2009 Sep 25.

Abstract

Myopia is one of the most common ocular disorders worldwide. Pathological myopia, also called high myopia, comprises 1% to 5% of the general population and is one of the leading causes of legal blindness in developed countries. To identify genetic determinants associated with pathological myopia in Japanese, we conducted a genome-wide association study, analyzing 411,777 SNPs with 830 cases and 1,911 general population controls in a two-stage design (297 cases and 934 controls in the first stage and 533 cases and 977 controls in the second stage). We selected 22 SNPs that showed P-values smaller than 10(-4) in the first stage and tested them for association in the second stage. The meta-analysis combining the first and second stages identified an SNP, rs577948, at chromosome 11q24.1, which was associated with the disease (P = 2.22x10(-7) and OR of 1.37 with 95% confidence interval: 1.21-1.54). Two genes, BLID and LOC399959, were identified within a 200-kb DNA encompassing rs577948. RT-PCR analysis demonstrated that both genes were expressed in human retinal tissue. Our results strongly suggest that the region at 11q24.1 is a novel susceptibility locus for pathological myopia in Japanese.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People / genetics
  • Chromosomes, Human, Pair 11 / genetics*
  • Female
  • Gene Expression Regulation
  • Genetic Markers
  • Genetic Predisposition to Disease*
  • Genome, Human / genetics
  • Genome-Wide Association Study*
  • HeLa Cells
  • Humans
  • Japan
  • Linkage Disequilibrium / genetics
  • Male
  • Middle Aged
  • Myopia, Degenerative / genetics*
  • Polymorphism, Single Nucleotide / genetics
  • Retina / metabolism
  • Retina / pathology

Substances

  • Genetic Markers