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. 2016 Oct 12;22:3658–3665. doi: 10.12659/MSM.896710

Table 3.

VEGF genotype and allele frequency in patients with cSCC (n=100) and control (n=124).

Groups Controls (n=124) Patients (n=100) P-value* OR (95% CI) P-value#
-1154460 C>T
 CC 51 (41.13%) 65 (65.00%) 1.00 (reference)
 CT 63 (50.81%) 31 (31.00%) 0.001 0.39 (0.22–0.68) 0.043
 TT 10 (8.06%) 4 (4.00%) 0.052 0.31 (0.09–1.06) 0.715
 TT+CT 73 (58.87%) 35 (35.00%) <0.001 0.36 (0.21–0.63) <0.001
Allele frequency
 C 165 (66.53%) 161 (80.50%) 1.00 (reference)
 T 83 (33.47%) 39 (19.50%) 0.001 0.48 (0.31–0.75)
-11541154 G>A
 GG 54 (43.55%) 51 (51.00%) 1.00 (reference)
 GA 58 (46.77%) 41 (41.00%) 0.305 0.75 (0.43–1.30) 0.247
 AA 12 (9.68%) 8 (8.00%) 0.482 0.71 (0.27–1.87) 0.654
 GA+AA 70 (56.45%) 49 (49.00%) 0.267 0.74 (0.44–1.26) 0.155
Allele frequency
 G 166 (66.94%) 143 (71.50%) 1.00 (reference)
 A 82 (33.06%) 57 (28.50%) 0.299 0.81 (0.54–1.21)

VEGF – vascular endothelial growth factor; OR – odds ratio; CI – confidence interval.

*

Two-sided χ2 test for distribution of genotypic and allelic frequencies.

#

Compared by binary logistic multivariate regression model with adjustment of sex and age for cases and controls.