Table II.
Polymorphism genotype or allele | Patients (n=100) | Controls (n=100) | OR | (95% CI) |
---|---|---|---|---|
Ser326Cys | ||||
CC | 22 | 29 | 1.00 | |
CG | 52 | 57 | 1.20 | (0.59–2.49) |
GG | 26 | 14 | 2.45 | (0.96–6.31) |
GG+CG | 78 | 71 | 1.45 | (0.73–2.90) |
C | 104 | 85 | 1.47 | (0.97–2.22) |
G | 96 | 115 | 1.00 | |
Arg156Arg | ||||
CC | 26 | 38 | 1.00 | |
AC | 53 | 49 | 1.58 | (0.80–3.13) |
AA | 21 | 13 | 2.36 | (0.93–6.08) |
AA+AC | 74 | 62 | 1.74 | (0.92–3.34) |
C | 95 | 75 | 1.51 | (0.99–2.29) |
A | 105 | 125 | 1.00 |
hOGG1, human homolog of the 8-oxoguanine DNA glycosylase 1; ERCC2/XPD, excision repair cross-complementing rodent repair deficiency complementation group 2/Xeroderma pigmentosum complementation group D; PCa, prostate cancer; OR, odds ratio; CI, confidence interval.