Table 1. Visual acuity change from baseline at one year among genotype groups of VEGFR2 SNPs rs4576072 and rs6828477 in CATT and IVAN.
Ranibizumab and Bevacizumab Combined | Ranibizumab only | |||||
---|---|---|---|---|---|---|
SNP Genotype | n (%) | Change in visual acuity (letters) Mean (SD) | P for comparison with TT§ | n (%) | Change in visual acuity (letters) Mean (SD) | P for comparison with TT§ |
CATT (N=835) | CATT (N=432) | |||||
rs4576072 | Linear Trend P=0.77 | Linear trend P=0.66 | ||||
TT | 595 (71) | 8.2 (14.5) | 312 (72) | 8.7 (12.8) | ||
CT | 219 (26) | 8.3 (13.6) | 0.90 | 111 (26) | 9.9 (12.5) | 0.41 |
CC | 21 (3) | 5.9 (11.3) | 0.46 | 9 (2) | 6.7 (13.0) | 0.63 |
CT or CC | 240 (29) | 8.1 (13.4) | 0.94 | 120 (28) | 9.6 (12.6) | 0.50 |
rs6828477 | Linear Trend P=0.20 | Linear trend P=0.01 | ||||
TT | 250 (30) | 9.2 (13.7) | 132 (31) | 10.6 (11.2) | ||
CT | 454 (54) | 7.8 (14.2) | 0.20 | 230 (53) | 9.1 (12.6) | 0.29 |
CC | 131 (16) | 7.5 (14.8) | 0.26 | 70 (16) | 5.5 (15.0) | 0.007 |
CT or CC | 585 (70) | 7.7 (14.4) | 0.16 | 300 (69) | 8.3 (13.3) | 0.09 |
IVAN (N=512)* | IVAN (N=271) | |||||
rs4576072 | Linear trend P=0.53 | Linear trend P= 0.56 | ||||
TT | 364 (71) | 6.0 (11.9) | 196 (72) | 6.4 (11.9) | ||
CT | 124 (24) | 4.2 (11.4) | 0.19 | 60 (22) | 5.6 (12.3) | 0.67 |
CC | 20 (4) | 7.4 (18.8) | 0.62 | 12 (4) | 11.5 (17.4) | 0.19 |
CT or CC | 144 (28) | 4.7 (12.5) | 0.30 | 72 (27) | 6.5 (13.0) | 0.93 |
rs6828477 | Linear trend P=0.97 | Linear trend P= 0.13 | ||||
TT | 185 (36) | 5.0 (12.0) | 95 (35) | 5.1 (12.8) | ||
CT | 221 (43) | 6.6 (11.8) | 0.22 | 121 (45) | 6.6 (11.2) | 0.39 |
CC | 105 (21) | 4.7 (12.8) | 0.81 | 55 (20) | 8.3 (13.2) | 0.14 |
CT or CC | 326 (64) | 5.9 (12.1) | 0.43 | 176 (65) | 7.2 (11.8) | 0.21 |
SD = standard deviation, SNP=single nucleotide polymorphism, VA=visual acuity.
CATT = Comparison of AMD Treatments Trials.
IVAN = Alternative Treatments to Inhibit VEGF in Patients with Age-Related Choroidal Neovascularization.
P values were calculated using analysis of variance.
Invalid genotype data occurred in 4 patients for rs4576072 and 1 patient for rs6828477 and were excluded from the statistical analysis.