Interaction of benzo[a]pyrene with other risk factors in hepatocellular carcinoma: a case-control study in Xiamen, China

被引:28
作者
Su, Yanhua [1 ]
Zhao, Benhua [1 ]
Guo, Fei [1 ]
Bin, Zhao [2 ]
Yang, Yue [1 ]
Liu, Sheng [1 ]
Han, Yaofeng [1 ]
Niu, Jianjun [3 ]
Ke, Xiayi [4 ]
Wang, Ning [5 ]
Geng, Xuesi [6 ]
Jin, Changnan [6 ]
Dai, Yichen [7 ]
Lin, Yuanyuan [7 ]
机构
[1] Xiamen Univ, Sch Publ Hlth, State Key Lab Mol Vaccinol & Mol Diagnost, Xiamen 361005, Fujian, Peoples R China
[2] Xiamen Univ, Organ Transplantat Inst, Xiamen 361005, Fujian, Peoples R China
[3] Xiamen Ctr Dis Control & Prevent, Xiamen, Fujian, Peoples R China
[4] UCL, Inst Child Hlth, London, England
[5] Xiamen Univ, Affiliated Hosp 1, Dept Hematol, Xiamen 361005, Fujian, Peoples R China
[6] Xiamen Hosp Tradit Chinese Med, Xiamen, Fujian, Peoples R China
[7] 174th Hosp Peoples Liberat Army, Digest Syst Dept, Xiamen, Fujian, Peoples R China
关键词
Hepatocellular carcinoma; Benzo[a]pyrene; DNA adduct; Case-control study; Risk factor; HEPATITIS-B-VIRUS; HYDROCARBON-DNA ADDUCTS; WHITE BLOOD-CELLS; AFLATOXIN EXPOSURE; LIVER-CANCER; BIOMARKERS; ALCOHOL; MARKERS; MUTATIONS; INFECTION;
D O I
10.1016/j.annepidem.2013.10.019
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose: Large epidemiologic studies about the relationship between benzo[a]pyrene (B[a]P) and hepatocellular carcinoma (HCC) have been limited. B[a]P diol epoxide (BPDE) is a highly reactive metabolite of B[a]P that binds covalently to form DNA adducts. We evaluated the interaction between B[a]P exposure with other risk factors in HCC, in a case-control study of 345 HCC and 961 healthy controls. Methods: Concentration of BPDE-DNA adducts in blood was determined by enzyme-linked immunosorbent assay. The interaction between BPDE-DNA adducts and other risk factors on HCC were evaluated by multivariate logistic regression analysis. Results: Mean concentration of BPDE-DNA adducts in blood of cases was significantly higher than that of the controls. The risk of HCC increased with elevated concentration of BPDE-DNA adducts (x(2) = 203.57, P-trend < .001) and the odds ratio was 7.44 (95% confidence interval, 5.29-10.45) for the first versus fourth quartile of adduct levels. The relative excess risk due to interaction between BPDE-DNA adducts and hepatitis B virus surface antigen and drinking was 34.71 and 54.92, and the attributable proportion due to interaction was 41.53% and 75.59%, respectively. Conclusions: The high level of BPDE-DNA adducts in blood is associated with HCC and that environmental exposure to B[a]P may increase the risk of HCC, especially among drinkers and populations with hepatitis B virus infection. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:98 / 103
页数:6
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