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. 2014 Jun 2;7(4):503–507. doi: 10.1016/j.tranon.2014.05.001

Table 2.

The Distribution of Frequencies of VDR Genotype and Haplotype Among Controls and Different Clinical Stages of Chronic HCV Infection

Con (n = 100) CH (n = 201) LC (n = 47) HCC (n = 92)
BsmI (rs1544410)
 TT 0 (0%) 0 (0%) 0 (0%) 0 (%)
 TC 11 (11%) 13 (6%) 6 (13%) 7 (8%)
 CC 89 (89%) 188 (94%) 41 (87%) 85 (92%)
 T vs. C allele 11:189 13:389 6:88 7:177
ApaI (rs7975232)
 CC 55 (55%)a 102 (51%)b 24 (51%)c 65 (71%)abc
 CA 40 (40%)d 82 (41%)e 19 (40%) 24 (26%)de
 AA 5 (5%) 17 (8%) 4 (9%) 3 (3%)
 C vs. A allele 150:50f 286:116g 67:27h 154:30fgh
TaqI (rs731236)
 GG 0 (0%) 0 (0%) 0 (0%) 0 (0%)
 AG 14 (14%) 15 (7%) 7 (15%) 6 (7%)
 AA 86 (86%) 186 (93%) 40 (85%) 86 (93%)
 G vs. A allele 14:186 15:387 7:87 6:178
BsmI–ApaI–TaqI
 TAG (BaT) 10 (10%) 12 (6%) 5 (11%) 5 (5%)
 CCA (bAt) 54 (54%)i 102 (51%)j 24 (51%)k 64 (70%)ijk
 CAA (bat) 31 (31%) 83 (41%)l 15 (32%) 21 (23%)l
 CAG (baT) 4 (4%) 3 (1%) 2 (4%) 0 (0%)
 TAA (Bat) 0 (0%) 1 (1%) 1 (2%) 1 (1%)
 TCG (BAT) 0 (0%) 0 (0%) 0 (0%) 1 (1%)
 TCA (BAt) 1 (1%) 0 (0%) 0 (0%) 0 (0%)
 CCA vs. TAG & CAA 54:41m 102:95n 24:20 64:26mn

Data are expressed as number (percentage). P-value by x2 test or Fisher’s exact test;

Abbreviation: VDR, vitamin D receptor; Con: healthy control; CH: chronic hepatitis; LC: liver cirrhosis; HCC: hepatocellular carcinoma.

a

P = 0.027; bP = 0.001; cP = 0.026; dP = 0.047; eP = 0.018; fP = 0.044; gP = 0.001; hP = 0.019; iP = 0.037; jP = 0.003; kP = 0.041; lP = 0.002; mP = 0.048; nP = 0.002