Association of the M55L and Q192R paraoxonase gene polymorphisms with age-related macular degeneration

被引:26
作者
Baird, PN
Chu, D
Guida, E
Vu, HTV
Guymer, R
机构
[1] Univ Melbourne, Ctr Eye Res Australia, Melbourne, Vic 3002, Australia
[2] Walter & Eliza Hall Inst Med Res, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Pharmacol, Mol Pharmacol Lab, Parkville, Vic 3052, Australia
关键词
D O I
10.1016/j.ajo.2004.04.053
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: To investigate the reported association of the two single,nucleotide polymorphisms (SNPs) of the paraoxonase gene (PON1), Met-Leu 55 (M55L) and Gln-Arg 192 (Q192R), in individuals of Anglo-Celtic descent who have age-related macular degeneration (AMD). DESIGN: Case-control association study. METHODS: Sixty-two individuals with late (end-stage) AMD and 115 control subjects (without AMD) were included in this study. The M55L and Q192R SNPs were amplified by polymerase chain reaction and genotyped, and statistical analysis was undertaken. RESULTS: No association of either SNP was detected in persons of Anglo-Celtic descent who had AMD, although there was a significant difference in SNP allele frequency between Anglo-Celtic and Japanese individuals. CONCLUSION: The M55L and Q192R SNPs of the PON1 gene do not appear to be associated with late AMD in individuals of Anglo-Celtic descent. (C) 2004 by Elsevier Inc. All rights reserved.
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收藏
页码:665 / 666
页数:2
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