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Original Article

Evaluation of Genetic Polymorphisms in Clusterin and Tumor Necrosis Factor-Alpha Genes in South Indian Individuals with Pseudoexfoliation Syndrome

, , , , &
Pages 1218-1224 | Received 07 Jul 2014, Accepted 08 Dec 2014, Published online: 07 Apr 2015
 

Abstract

Purpose: The aim of this study was to explore the potential association of genetic variants across clusterin (CLU) and tumor necrosis factor-alpha (TNF-α) genes in South Indian individuals with pseudoexfoliation syndrome (PEXS) and pseudoexfoliation glaucoma (PEXG).

Materials and Methods: A total of 523 individuals including 299 unrelated cases (150 PEXS and 149 PEXG) and 224 age- and ethnically-matched healthy controls were recruited for genetic analysis. Six single-nucleotide polymorphisms (SNPs) including, five CLU SNPs (rs11136000, rs2279590, rs9331888, rs9331931, rs3087554) and one promoter SNP (rs1800629) of TNF-α were genotyped in all study subjects. Genotyping of CLU SNPs were performed using the TaqMan allelic discrimination assay while TNF-α SNP was genotyped using polymerase chain reaction (PCR)-based restriction fragment length polymorphism (RFLP) analysis. Association analysis was performed by determining the distributions of genotype and allele frequencies, Hardy–Weinberg equilibrium, and chi-square p values and odds ratios as implemented in the Golden Helix SNP & Variation Suite (SVS).

Results: Five CLU SNPs did not show any significant differences in allele frequencies between patients and control subjects (rs3087554, p = 0.919, OR = 1.01, 95% CI: 0.77–1.33; rs2279590, p = 0.432, OR = 1.12, 95% CI: 0.84–1.51; rs9331931, p = 0.310, OR = 1.24, 95% CI: 0.81–1.89; rs11136000, p = 0.072, OR = 1.31, 95% CI: 0.97–1.76; rs9331888, p = 0.911, OR = 1.01, 95% CI: 0.78–1.31). The investigation of TNF-α SNP established a significant association with PEXS and PEXG (p = 0.042, OR = 0.61, 95% CI: 0.38–0.99). However, this association did not remain significant after Bonferroni correction.

Conclusions: Our data suggest that genetic variants in CLU and TNF-α genes do not play a major role in the development of PEXS and PEXG in the South Indian population.

Acknowledgments

The authors thank all the patients and healthy subjects for participating in this study.

Declaration of interest

This study was supported by research grant from ALCON – Aravind Eye Care System, India. The authors have no competing interests to declare.

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