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. Author manuscript; available in PMC: 2018 Jun 28.
Published in final edited form as: J Hepatol. 2010 Jun 20;53(4):671–676. doi: 10.1016/j.jhep.2010.04.032

Table 4.

HCC risks in relation to HBV mutations and AFB1 exposure in cases and controls.

BCP Mutations AFB1-lysine adduct Controls (%) Cases (%) OR (95% CI) Adjusted OR (95%CI)*
1762T/1764A double mutations or 1762T single mutations Concentration (pgrfmg alb.)
 No <6.46 22(18.3) 3 (5.0) 1.00 1.00
≥6.46 9 (7.5) 2 (3.3) 1.63 (0.23–11.45) 2.01 (0.24–14.49)
 Yes <6.46 66 (55.0) 36 (60.0)** 4.00(1.12–14.27) 4.26 (1.16–15.38)
≥6.46 23(19.2) 19(31.7)** 6.06(1.57–23.37) 6.94 (1.68–27.78)
1752V mutations Concentration (pg/mg alb.)
 No <6.46 65 (54.2) 21(35.0) 1.00 1.00
≥6.46 24 (20.0) 9 (15.0) 1.16(0.47–2.89) 1.20 (0.47–3.08)
 Yes <6.46 23(19.2) 18(30.0)** 2.42(1.10–5.33) 2.28(1.01–5.31)
≥6.46 8 (6.7) 12(20.0)** 4.65(1.67–12.89) 5.13 (1.79–14.71)
*

adjusted for age, gender, first-degree family history of cancer

**

p <0.05 from unconditional logistic regression in comparison with baseline group (no mutation and lower than average AFB1-lysin adduct)