Table 1.
Gene SNP |
Model | Genotype | Genotype Frequencies, n (%) a | Unadjusted | Adjusted b | Adjusted c | ||||
---|---|---|---|---|---|---|---|---|---|---|
Controls | Cases | OR (95% CI) | p | OR (95% CI) | p | OR (95% CI) | p | |||
TLR4 | Codominant | AA | 128 (98.5) | 56 (80.0) | 1.00 | <0.0001 | 1.00 | 0.0005 | 1.00 | 0.0085 |
rs4986790 | AG | 2 (1.5) | 13 (18.6) | 14.86 (3.24–68.03) | 14.40 (2.99–69.41) | 8.83 (1.54–50.53) | ||||
GG | 0 (0) | 1 (1.4) | NA (0.00–NA) | 11.77 (0.00–NA) | NA (0.00–NA) | |||||
Dominant | AA | 128 (98.5) | 56 (80) | 1.00 | <0.0001 | 1.00 | 0.0001 | 1.00 | 0.003 | |
AG-GG | 2 (1.5) | 14 (20) | 16.00 (3.52–72.76) | 14.40 (2.99–69.41) | 11.03 (2.04–59.72) | |||||
Recessive | AA-AG | 130 (100) | 69 (98.6) | 1.00 | 0.15 | 1.00 | 1 | 1.00 | 0.075 | |
GG | 0 (0) | 1 (1.4) | NA (0.00–NA) | 11.30 (0.00–NA) | NA (0.00–NA) | |||||
Overdominant | AA-GG | 128 (98.5) | 57 (81.4) | 1.00 | <0.0001 | 1.00 | 0.0001 | 1.00 | 0.013 | |
AG | 2 (1.5) | 13 (18.6) | 14.60 (3.19–66.81) | 14.40 (2.99–69.41) | 8.53 (1.49–48.78) | |||||
TLR4 | Codominant | CC | 119 (91.54) | 63 (90.0) | 1.00 | 0.35 | 1.00 | 0.87 | 1.00 | 1 |
rs4986791 | CT | 11 (8.5) | 6 (8.6) | 1.03 (0.36–2.92) | 0.71 (0.19–2.64) | 1.05 (0.28–3.98) | ||||
TT | 0 (0) | 1 (1.4) | NA (0.00–NA) | 0.00 (0.00–NA) | 0.00 (0.00–NA) | |||||
Dominant | CC | 119 (91.5) | 63 (90.0) | 1.00 | 0.72 | 1.00 | 0.59 | 1.00 | 0.95 | |
CT-TT | 11 (8.5) | 7 (10.0) | 1. 20 (0.44–3.25) | 0.71 (0.19–2.64) | 1.05 (0.28–3.98) | |||||
Recessive | CC-CT | 130 (100) | 69 (98.6) | 1.00 | 0.15 | 1.00 | 1 | 1.00 | 1 | |
TT | 0 (0) | 1 (1.4) | NA (0.00–NA) | 0.00 (0.00–NA) | 0.00 (0.00–NA) | |||||
Overdominant | CC-TT | 119 (91.5) | 64 (91.4) | 1.00 | 0.98 | 1.00 | 0.59 | 1.00 | 0.95 | |
CT | 11 (8.5) | 6 (8.6) | 1.01 (0.36–2.87) | 0.71 (0.19–2.64) | 1.05 (0.28–3.98) | |||||
TLR9 | Codominant | TT | 35 (28.2) | 15 (22.4) | 1.00 | 0.091 | 1.00 | 0.14 | 1.00 | 0.85 |
rs187084 | TC | 81 (65.3) | 41 (61.2) | 1.18 (0.58–2.41) | 0.90 (0.41–1.94) | 0.96 (0.40–2.32) | ||||
CC | 8 (6.5) | 11 (16.4) | 3.21 (1.08–9.57) | 2.69 (0.84–8.66) | 1.46 (0.32–6.64) | |||||
Dominant | TT | 35 (28.2) | 15 (22.4) | 1.00 | 0.38 | 1.00 | 0.88 | 1.00 | 0.99 | |
TC-CC | 89 (71.8) | 52 (77.6) | 1.36 (0.68–2.73) | 1.06 (0.50–2.23) | 1.00 (0.42–2.38) | |||||
Recessive | TT-TC | 116 (93.5) | 56 (83.6) | 1.00 | 0.032 | 1.00 | 0.049 | 1.00 | 0.58 | |
CC | 8 (6.5) | 11 (16.4) | 2.85 (1.09–7.48) | 2.90 (1.02–8.24) | 1.50 (0.37–6.01) | |||||
Overdominant | TT-CC | 43 (34.7) | 26 (38.8) | 1.00 | 0.57 | 1.00 | 0.27 | 1.00 | 0.77 | |
TC | 81 (65.3) | 41 (61.2) | 0.84 (0.45–1.55) | 0.68 (0.35–1.35) | 0.88 (0.40–1.98) |
a Values are the number of examined healthy women (controls) and those with OC (cases). (%); b Adjusted analysis was carried out for HPV16 DNA copy number in whole-blood samples; c Adjusted analysis was carried out for HPV18 DNA copy number in whole-blood samples; OR: odds ratio; 95% CI: 95% confidence interval; p, logistic regression model; NA: not available; PB, The significance level after Bonferroni’s correction for multiple testing was 0.017 (raw p-value/3).