[Association between LOXL1 gene polymorphisms and primary open angle glaucoma in Sichuan population]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):89-93. doi: 10.3760/cma.j.issn.1003-9406.2015.01.020.
[Article in Chinese]

Abstract

Objective: To investigate association between the lysyl oxidase-like 1 (LOXL1) gene single nucleotide polymorphism (SNP) and primary open-angle glaucoma (POAG) in Sichuan population.

Methods: In this study,416 subjects with primary open-angle glaucoma and 997 normal controls were recruited.Three reported LOXL1 tag SNPs (rs1048661,rs3825942 and rs2165241) were genotyped by SNaPshot method.

Results: The study showed that the genotypes of LOXL1 rs1048661,rs3825942 and rs2165241 between POAG and control groups were not statistically significant (OR=1.085, 95%CI 0.92-1.28, P=0.578 for rs1048661; OR=1.059, 95%CI 0.82-1.37, P=0.846 for rs3825942; OR=1.006, 95%CI 0.77-1.32, P=0.966 for rs2165241, respectively). There were no significant difference in allele frequency distribution of LOXL1 rs1048661、rs3825942 and rs2165241 between POAG and normal controls (P=0.322, P=0.660, P=0.965).

Conclusion: The results from the present study do not indicate the association of LOXL1 SNPs (rs1048661, rs3825942 and rs2165241) with POAG in Sichuan population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Amino Acid Oxidoreductases / genetics*
  • Asian People / genetics*
  • Glaucoma, Open-Angle / genetics*
  • Humans
  • Middle Aged
  • Polymorphism, Single Nucleotide*

Substances

  • Amino Acid Oxidoreductases
  • LOXL1 protein, human