PURPOSE: To study the relationships between single nucleotide polymorphisms (SNPs) of extracellular matrix, matrix metalloproteases (MMPs), tissue inhibitors of MMPs, and other glaucoma-associated genes and acute primary angle closure glaucoma (PACG). METHODS: We extracted DNA samples from 78 adult patients with acute PACG and 86 control subjects to study the relationships between these specific genes and acute PACG. Genotyping was performed for 35 genes by the GenomeLab SNPstream genotyping system after PCR amplification of chromosomal DNA. The association between these genetic polymorphisms and risk of primary PACG was estimated by chi2 and logistic regression. RESULTS: The genotyping success rate was 99%. Genotyping for the MMP9 site (rs2664538) was significantly different between the two groups (p=0.000001) and the odds ratio was 2.586 (95% CI: 1.715-3.898, p<0.00001). However, there were no associations of SNPs to other genes in patients with acute PACG. CONCLUSIONS: Our results reveal that SNP rs2664538, which is located at the MMP9 gene, is likely to be associated with acute PACG.
PURPOSE: To study the relationships between single nucleotide polymorphisms (SNPs) of extracellular matrix, matrix metalloproteases (MMPs), tissue inhibitors of MMPs, and other glaucoma-associated genes and acute primary angle closure glaucoma (PACG). METHODS: We extracted DNA samples from 78 adult patients with acute PACG and 86 control subjects to study the relationships between these specific genes and acute PACG. Genotyping was performed for 35 genes by the GenomeLab SNPstream genotyping system after PCR amplification of chromosomal DNA. The association between these genetic polymorphisms and risk of primary PACG was estimated by chi2 and logistic regression. RESULTS: The genotyping success rate was 99%. Genotyping for the MMP9 site (rs2664538) was significantly different between the two groups (p=0.000001) and the odds ratio was 2.586 (95% CI: 1.715-3.898, p<0.00001). However, there were no associations of SNPs to other genes in patients with acute PACG. CONCLUSIONS: Our results reveal that SNP rs2664538, which is located at the MMP9 gene, is likely to be associated with acute PACG.
Authors: Ralph J Hazlewood; Benjamin R Roos; Frances Solivan-Timpe; Robert A Honkanen; Lee M Jampol; Stephen C Gieser; Kacie J Meyer; Robert F Mullins; Markus H Kuehn; Todd E Scheetz; Young H Kwon; Wallace L M Alward; Edwin M Stone; John H Fingert Journal: Hum Mutat Date: 2015-03 Impact factor: 4.878
Authors: Elizabeth M Perruccio; Laura Leigh S Rowlette; Nuria Comes; Silvia Locatelli-Hoops; Luigi Notari; S Patricia Becerra; Teresa Borrás Journal: Curr Eye Res Date: 2008-05 Impact factor: 2.424
Authors: Georg Mossböck; Martin Weger; Christoph Faschinger; Christine Zimmermann; Otto Schmut; Wilfried Renner; Yosuf El-Shabrawi Journal: Mol Vis Date: 2010-08-28 Impact factor: 2.367