Association of Base Excision Repair Gene Polymorphisms with ESRD Risk in a Chinese Population
Table 3
Combined analysis of genetic polymorphisms in OGG1 and MUTYH with HD risk.
Genotypes
Patients ()
Controls ()
P valuec
OR (95% CI)
MUTYH c.972GGa
OGG1
c.977CC
23 (6.8%)
27 (6.7%)
0.939
1.02 (0.58–1.82)
c.977CG
67 (19.9%)
75 (18.6%)
0.650
1.09 (0.75–1.57)
c.977GG
48 (14.2%)
28 (6.9%)
0.001
2.23 (1.37–3.64)
AluYb8MUTYH
A/A
18 (5.3%)
19 (4.7%)
0.691
1.14 (0.59–2.22)
A/P
58 (17.2%)
54 (13.4%)
0.146
1.35 (0.90–2.02)
P/P
62 (18.4%)
57 (14.1%)
0.113
1.37 (0.93–2.03)
AluYb8MUTYHA/P or P/P
b
OGG1
c.977CC
38 (11.3%)
42 (10.4%)
0.701
1.10 (0.69–1.74)
c.977CG
120 (35.6%)
136 (33.7%)
0.579
1.09 (0.80–1.48)
c.977GG
78 (23.1%)
75 (18.6%)
0.125
1.32 (0.93–1.89)
MUTYH
c.972CC
11 (3.3%)
12 (3.0%)
0.818
1.10 (0.48–2.53)
c.972CG
105 (31.2%)
130 (32.2%)
0.766
0.95 (0.70–1.30)
c.972GG
120 (35.6%)
111 (27.5%)
0.017
1.46 (1.07–1.99)
Note: CI: confidence interval; OR: odds ratio. Trend test assessing correlation between HD risk and predicted high-risk OGG1 and MUTYH genotypes combined with the MUTYH c.972GG genotype. Trend test assessing correlation between HD risk and predicted high-risk OGG1 and MUTYH genotypes combined with the AluYb8MUTYH A/P or P/P genotype. c: value for comparison using χ 2-test between patients and controls.