Table 2 The distribution of NOS3, EDN1 and EDNRA genotypes according to the presence and severity of retinopathy of prematurity (ROP).
Genotype | Incidence and outcome of ROP | Statistical Analysis I + II vs. III OR (95%CI); P | ||
---|---|---|---|---|
I No ROP N = 105 | II ROP not requiring treatment; N = 90 | III ROP requiring treatment; N = 90 | ||
NOS3 rs2070744 T > C | ||||
TT | 43 (41.0) | 31 (34.4) | 41 (45.6) | Studied effect: Dom. 0.73 (0.44–1.2), 0.224 Rec. 0.34 (0.15 − 0.79), 0.009a Allele freq. 0.65 (0.45–0.95), 0.023 |
TC | 43 (41.0) | 39 (43.3) | 42 (46.7) | |
CC | 19 (18.0) | 20 (22.3) | 7 (7.7) | |
MAF; PHWE | 0.386; 0.614 | 0.439; 0.561 | 0.311; 0.689 | |
NOS3 rs1799983 G > T (Glu298Asp) | ||||
GG | 54 (52.0) | 51 (56.7) | 48 (53.3) | Studied effect: Dom. 1.0 (0.63–1.7), 0.901 Rec. 1.4 (0.59–3.4), 0.424 Allele freq. 1.1 (0.77–1.6), 0.656 |
GT | 42 (40.4) | 33 (36.7) | 33 (36.7) | |
TT | 8 (7.6) | 6 (6.6) | 9 (10.0) | |
MAF; PHWE | 0.279; 0.721 | 0.250; 0.750 | 0.283; 0.717 | |
NOS3 rs2070744/rs1799983 | ||||
TT + TC/GG + GT | 83 (79.8) | 67 (74.4) | 77 (85.6) | 1.0 (Reference) 0.26 (0.09–0.76), 0.009b 1.95 (0.61–6.2), 0.254 0.73 (0.19–2.8), 0.649 |
CC/GG + GT | 13 (12.5) | 17 (18.9) | 4 (4.4) | |
TT + TC/TT | 3 (2.9) | 3 (3.3) | 6 (6.7) | |
CC/TT | 5 (4.8) | 3 (3.3) | 3 (3.3) | |
EDN1 rs5370 G > T | ||||
GG | 70 (66.7) | 59 (65.6) | 55 (62.5) | Studied effect: Dom. 1.2 (0.70–2.0). 0.551 Rec. 1.1 (0.33–3.8). 0.864 Allele 1.1 (0.73–1.8). 0.570 |
GT | 29 (27.6) | 29 (32.2) | 29 (33.0) | |
TT | 6 (6.6) | 2 (2.2) | 4 (4.5) | |
MAF; PHWE | 0.195; 0.805 | 0.183; 0.817 | 0.210; 0.790 | |
EDNRA rs5335 G > C | ||||
GG | 30 (28.8) | 23 (26.1) | 25 (28.1) | Studied effect: Dom. 0.96 (0.55–1.7). 0.893 Rec. 1.1 (0.58–2.0). 0.810 Allele 1.0 (0.71–1.4). 0.958 |
CG | 54 (52.0) | 46 (52.3) | 45 (50.6) | |
CC | 20 (19.2) | 19 (21.6) | 19 (21.3) | |
MAF; PHWE | 0.452; 0.452 | 0.477; 0.477 | 0.466; 0.466 |