Association between variants A69S in ARMS2 gene and response to treatment of exudative AMD: a meta-analysis

被引:22
作者
Hu, Zizhong [1 ]
Xie, Ping [1 ]
Ding, Yuzhi [1 ]
Yuan, Dongqing [1 ]
Liu, Qinghuai [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Ophthalmol, Nanjing 210029, Jiangsu, Peoples R China
关键词
AGE-RELATED MACULOPATHY; COMPLEMENT FACTOR-H; POLYPOIDAL CHOROIDAL VASCULOPATHY; GROWTH-FACTOR TREATMENT; MACULAR DEGENERATION; INTRAVITREAL RANIBIZUMAB; LOC387715/HTRA1; VARIANTS; PHOTODYNAMIC THERAPY; SUSCEPTIBILITY; BEVACIZUMAB;
D O I
10.1136/bjophthalmol-2014-305488
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
A study was undertaken to investigate the association between A69S in age-related maculopathy susceptibility 2 (ARMS2) and the response to anti-angiogenesis treatment in exudative age-related macular degeneration (AMD). A literature-based meta-analysis was performed of studies relevant to A69S and the response to anti-angiogenesis treatment. PubMed, Web of Science, China National Knowledge Infrastructure (CNKI) and Sinomed databases were used to retrieve articles up to July 2014. Pooled ORs and 95% CIs were estimated using fixed and random effects models in Stata V.9.0. Q-statistic testing was used to assess heterogeneity. Twelve articles comprising 2389 cases were included in the final meta-analysis. The analysis of the overall population indicated a statistically significant association between A69S and the response to anti-angiogenesis treatment in exudative AMD (GG vs TT: OR 1.34 (95% CI 1.01 to 1.77), p=0.039; GT vs TT: OR 1.58 (95% CI 1.08 to 2.31), p=0.018; GG+GT vs TT: OR 1.74 (95% CI 1.19 to 2.52), p=0.004). In subgroup analysis, A69S appeared more likely to be a predictor for anti-angiogenic response in the East Asian population (GG vs TT: OR 1.65 (95% CI 1.02 to 2.68), p=0.042; GT vs TT: OR 1.66 (95% CI 1.17 to 2.37), p=0.005; GG+GT vs TT: OR 1.82 (95% CI 1.07 to 3.10), p=0.027; G vs T: OR 1.56 (95% CI 1.01 to 2.41)). However, no statistical significance was found in the Caucasian subgroup analysis. This study shows an association between A69S polymorphism in the ARMS2 gene and the anti-angiogenesis treatment response. A69S could be considered predictive of the anti-angiogenic effects, especially in Asian populations.
引用
收藏
页码:593 / 598
页数:6
相关论文
共 46 条
[1]   Genetic Influences on the Outcome of Anti-Vascular Endothelial Growth Factor Treatment in Neovascular Age-related Macular Degeneration [J].
Abedi, Farshad ;
Wickremasinghe, Sanjeewa ;
Richardson, Andrea J. ;
Islam, Amirul F. M. ;
Guymer, Robyn H. ;
Baird, Paul N. .
OPHTHALMOLOGY, 2013, 120 (08) :1641-1648
[2]  
Anand R, 2000, OPHTHALMOLOGY, V107, P2224
[3]  
[Anonymous], 2012, INVESTIG OPHTHALMOL
[4]   Intravitreal bevacizumab (Avastin) for neovascular age-related macular degeneration [J].
Avery, RL ;
Pieramici, DJ ;
Rabena, MD ;
Castellarin, AA ;
Nasir, MA ;
Giust, MJ .
OPHTHALMOLOGY, 2006, 113 (03) :363-372
[5]  
Bessho H, 2011, MOL VIS, V17, P977
[6]   Association of complement factor H and LOC387715 genotypes with response of exudative age-related macular degeneration to intravitreal bevacizumab [J].
Brantley, Milam A., Jr. ;
Fang, Amy M. ;
King, Jennifer M. ;
Tewari, Asheesh ;
Kymes, Steven M. ;
Shiels, Alan .
OPHTHALMOLOGY, 2007, 114 (12) :2168-2173
[7]   Ranibizumab versus verteporfin for neovascular age-related macular degeneration [J].
Brown, David M. ;
Kaiser, Peter K. ;
Michels, Mark ;
Soubrane, Gisele ;
Heier, Jeffrey S. ;
Kim, Robert Y. ;
Sy, Judy P. ;
Schneider, Susan .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (14) :1432-1444
[8]   Association between Variant Y402H in Age-Related Macular Degeneration (AMD) Susceptibility Gene CFH and Treatment Response of AMD: A Meta-Analysis [J].
Chen, Han ;
Yu, Ke-Da ;
Xu, Ge-Zhi .
PLOS ONE, 2012, 7 (08)
[9]   Genetic and Functional Dissection of ARMS2 in Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy [J].
Cheng, Yong ;
Huang, LvZhen ;
Li, Xiaoxin ;
Zhou, Peng ;
Zeng, Wotan ;
Zhang, ChunFang .
PLOS ONE, 2013, 8 (01)
[10]   Mechanisms of disease: Age-related macular degeneration [J].
de Jong, Paulus T. V. M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (14) :1474-1485