Colorectal Cancer
Copyright ©2005 Baishideng Publishing Group Inc.
World J Gastroenterol. Jun 7, 2005; 11(21): 3250-3254
Published online Jun 7, 2005. doi: 10.3748/wjg.v11.i21.3250
Table 1 OR and 95%CI for CRC with UGT1A7 genotypes and alleles.
UGT1A7 genotype or alleleNumber (%)
OR (95%CI)P
Cases (n = 268)Controls (n = 441)
UGT1A7*1/*176 (28.4)184 (41.7)0.55 (0.40-0.77)<0.001
UGT1A7*1/*273 (27.2)117 (26.5)1.04 (0.74-1.46)0.84
UGT1A7*1/*377 (28.7)75 (17.0)1.97 (1.37-2.83)<0.001
UGT1A7*2/*29 (3.4)22 (5.0)0.66 (0.30-1.46)0.31
UGT1A7*2/*323 (8.6)32 (7.3)1.20 (0.69-2.10)0.52
UGT1A7*3/*310 (3.7)11 (2.5)1.52 (0.64-3.62)0.35
UGT1A7*1226 (84.3)376 (85.3)1.08 (0.71-1.64)0.74
UGT1A7*2105 (39.2)171 (38.8)1.02 (0.75-1.39)0.92
UGT1A7*3110 (41.0)118 (26.8)1.91 (1.38-2.63)<0.001
Table 2 The comparisons between the observed percentage with the expected percentage of control subjects carrying UGT1A7*1/*2, UGT1A7*1/*3, and UGT1A7*2/*3 genotypes.
Control subjects (n = 441)
χ2P
Observed percentage (%)Expected percentage (%)1
UGT1A7*1/*226.528.90.0810.960
UGT1A7*1/*317.020.4
UGT1A7*2/*37.37.1
Table 3 The comparison of UGT1A1 genotypes between case and control groups.
UGT1A1 genotypeCase group (n = 268)
Control group (n = 441)
P2 test)
Number%Number%
Wild type12145.221849.40.78
Heterozygous variation11844.018642.23
6/713796
211 G to A/normal7679
1091 C to T/normal511
Compound heterozygous variation238.6347.7
6/7, 211 G to A/normal136
6/7, 686 C to A/normal820
6/7, 1091 C to T/normal02
6/7, 211 G to A/normal,12
686 C to A/normal 6/7,
686 C to A/normal,10
1091 C to T/normal
211 G to A/normal,04
1091 C to T/normal
Homozygous variation62.230.7
7/7210
211 G to A/211 G to A43
7/7, 211 G to A/normal10
Table 4 OR and 95%CI for CRC with UGT1A1 alleles.
UGT1A1 alleleNumber (%)
OR (95%CI)P
Cases (n = 268)Controls (n = 441)
A(TA)7TAA62 (23.1)126 (28.6)0.75 (0.52-1.05)0.09
Variant-21195 (35.4)94 (21.3)2.03 (1.45-2.84)<0.001
Variant 68610 (3.7)22 (5.0)0.74 (0.34-1.58)0.44
Variant 10916 (2.2)17 (3.8)0.57 (0.22-1.47)0.25
Table 5 The interaction effect of the UGT1A7*3 allele and variant-211 UGT1A1 allele upon the development of CRC.
UGT1A7*3/ variant-211UGT1A1Number (%)
OR (95%CI)P
Cases (n = 268)Controls (n = 441)
Absent/absent145 (54.1)302 (68.5)1.00
Present/absent28 (10.4)45 (10.2)1.30 (0.78-2.16)0.39
Absent/present13 (4.8)21 (4.8)1.29 (0.63-2.65)0.33
Present/present82 (30.6)73 (16.5)2.34 (1.61-3.40)<0.001
Expected by additive11.59
Table 6 OR and 95%CI of stages-C and -D CRCs with CRC-related UGT1A alleles.
CRC-related alleleStage of CRC
OR (95%CI)P
C and D (n = 93)A and B(n = 175)
UGT1A7*3611 (65.6%)49 (28.0%)4.90 (2.86-8.41)<0.001
Variant-211 UGT1A1551 (59.1%)40 (22.9%)4.89 (2.84-8.41)<0.001
Table 7 Adjusted odds ratios (AOR) and 95%CI for the different stages of CRC with age, gender, and CRC-related UGT1A alleles.
FactorCRC stage
OR (95%CI)P
C and D (n = 93)A and B (n = 175)
Age >51/ ≤50 yr79/14155/200.68 (0.31-1.53)0.35
Gender male/female55/3885/901.44 (0.82-2.51)0.20
UGT1A7*361 (65.6%)49 (28.0%)2.51 (1.23-5.13)0.01
Variant-211 UGT1A155 (59.1%)40 (22.9%)2.71 (1.31-5.58)0.01
Table 8 The interaction effect of the UGT1A7*3 allele and variant-211 UGT1A1 allele upon the stage of CRC.
UGT1A7*3/variant-211UGT1A1CRC stage
OR (95%CI)P
C and D (n = 93)A and B (n = 175)
Absent/absent27 (29.0%)118 (67.4%)1.00
Present/absent11 (11.8%)17 (9.7%)2.83 (1.19-6.72)0.02
Absent/present5 (5.4%)8 (4.6%)2.73 (0.83-9.01)0.10
Present/present50 (53.8%)32 (18.3%)6.83 (3.71-12.56)<0.001
Expected by additive14.56