Toll-like Receptor Polymorphisms and Age-Related Macular Degeneration: Replication in Three Case-Control Samples

被引:48
作者
Cho, Youngeun [1 ]
Wang, Jie Jin [3 ,4 ]
Chew, Emily Y. [2 ]
Ferris, Frederick L., III [2 ]
Mitchell, Paul [3 ,4 ]
Chan, Chi-Chao [1 ]
Tuo, Jingsheng [1 ]
机构
[1] NEI, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] NEI, Div Epidemiol & Clin Applicat, NIH, Bethesda, MD 20892 USA
[3] Univ Sydney, Ctr Vis Res, Dept Ophthalmol, Westmead, NSW 2145, Australia
[4] Univ Sydney, Westmead Millennium Inst, Westmead, NSW 2145, Australia
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
GEOGRAPHIC ATROPHY; VISUAL-LOSS; FACTOR-H; PREVALENCE; AUSTRALIA; VARIANT; TLR4;
D O I
10.1167/iovs.09-3688
中图分类号
R77 [眼科学];
学科分类号
100212 [眼科学];
摘要
PURPOSE. Innate immunity appears to play a key role in age-related macular degeneration (AMD). Although two previous studies reported that gene variations in Toll-like receptor (TLR)-3 and -4 are associated with AMD, other studies have not confirmed these associations. In this study, three independent samples (two U. S. clinic-based case-control study samples and one Australian population-based study sample) were used to further assess the association of the polymorphisms rs3775291 in TLR3 and rs4986790 in TLR4 with AMD. METHODS. AMD cases and unrelated controls were collected from the National Eye Institute Clinical Center (NEI, n = 320), the Age-Related Eye Disease Study (AREDS, n = 483), and the Blue Mountains Eye Study (BMES, n = 852). DNA extracted from subjects was genotyped for rs3775291 and rs4986790, and the associations with AMD were investigated. RESULTS. Neither of the two polymorphisms rs3775291 and rs4986790 had a statistically significant association with AMD in any of the three sample sets or in combinations of the sets. Analysis of the combined geographic atrophy or neovascular AMD cases in the NEI, AREDS, and BMES sample sets also failed to demonstrate statistically significant associations of those two single nucleotide polymorphisms with advanced AMD. CONCLUSIONS. Even with previously verified samples sets and adequate study powers, the results did not confirm the reported associations of TLR3 rs3775291 and TLR4 rs4986790 with AMD in the three independent samples, individually or combined. (Invest Ophthalmol Vis Sci. 2009; 50: 5614-5618) DOI: 10.1167/iovs.09-3688
引用
收藏
页码:5614 / 5618
页数:5
相关论文
共 28 条
[1]
Allikmets R, 2009, NEW ENGL J MED, V360, P2252
[2]
Anand R, 2000, OPHTHALMOLOGY, V107, P2224
[3]
Arancibia SA, 2007, BIOL RES, V40, P97, DOI 10.4067/S0716-97602007000200001
[4]
Attebo K, 1996, OPHTHALMOLOGY, V103, P357
[5]
Meta-analysis of the association of the HTRA1 polymorphisms with the risk of age-related macular degeneration [J].
Chen, Wen ;
Xu, Wei ;
Tao, Qiushan ;
Liu, Juan ;
Li, Xiaojing ;
Gan, Xiumin ;
Hu, Honglin ;
Lu, Yunxia .
EXPERIMENTAL EYE RESEARCH, 2009, 89 (03) :292-300
[6]
Davis MD, 2005, ARCH OPHTHALMOL-CHIC, V123, P1484
[7]
Comprehensive analysis of the candidate genes CCL2, CCR2, and TLR4 in age-related macular degeneration [J].
Despriet, Dominiek D. G. ;
Bergen, Arthur A. B. ;
Merriam, Joanna E. ;
Zernant, Jana ;
Barile, Gaetano R. ;
Smith, Theodore ;
Barbazetto, Irene A. ;
van Soest, Simone ;
Bakker, Arne ;
de Jong, Paulus T. V. M. ;
Allikmets, Rando ;
Klaver, Caroline C. W. .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2008, 49 (01) :364-371
[8]
Molecular pathology of age-related macular degeneration [J].
Ding, Xiaoyan ;
Patel, Mrinali ;
Chan, Chi-Chao .
PROGRESS IN RETINAL AND EYE RESEARCH, 2009, 28 (01) :1-18
[9]
Toll-like receptor polymorphisms and age-related macular degeneration [J].
Edwards, Albert O. ;
Chen, Dequan ;
Fridley, Brooke L. ;
James, Katherine M. ;
Wu, Yanhong ;
Abecasis, Goncalo ;
Swaroop, Anand ;
Othman, Mohammad ;
Branham, Kari ;
Iyengar, Sudha K. ;
Sivakumaran, Theru A. ;
Klein, Ronald ;
Klein, Barbara E. K. ;
Tosakulwong, Nirubol .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2008, 49 (04) :1652-1659
[10]
Edwards AO, 2009, NEW ENGL J MED, V360, P2254