Literature DB >> 29479565

Qidong hepatitis B virus infection cohort: a 25-year prospective study in high risk area of primary liver cancer.

Taoyang Chen1, Gengsun Qian2, Chunsun Fan1,2, Yan Sun1, Jinbing Wang1, Peixin Lu1, Xuefeng Xue1, Yan Wu1, Qinan Zhang1, Yan Jin2, Yiqian Wu2, Yu Gan2, Jianquan Lu1, Thomas W Kensler3, John D Groopman3, Hong Tu2.   

Abstract

Qidong hepatitis B virus (HBV) infection cohort (QBC) is a prospective community-based study designed to investigate causative factors of primary liver cancer (PLC) in Qidong, China, where both PLC and HBV infection are highly endemic. Residents aged 20-65 years, living in seven townships of Qidong, were surveyed using hepatitis B surface antigen (HBsAg) serum test and invited to participate in QBC from June 1991 to December 1991. A total of 852 and 786 participants were enrolled in HBsAg-positive and HBsAg-negative sub-cohorts in May 1992, respectively. All participants were actively followed up in person, received HBsAg, alanine aminotransferase (ALT), alpha-fetoprotein (AFP) tests and upper abdominal ultrasonic examination, and donated blood and urine samples once or twice a year. The total response rate was 99.6%, and the number of incident PLC was 201 till the end of February 2017. The ratio of incidence rates was 12.32 (95% confidence interval[CI]=7.16-21.21, P < 0.0001) in HBsAg-positive arm compared with HBsAg-negative arm. The relative risk of PLC was 13.25 (95% CI=6.67-26.33, P < 0.0001) and 28.05 (95% CI=13.87-56.73, P < 0.0001) in the HBsAg+/HBeAg- group and the HBsAg+/HBeAg+ group, respectively, as compared to the HBsAg-/HBeAg- group. A series of novel PLC-related mutations including A2159G, A2189C and G2203W at the C gene, A799G, A987G and T1055A at the P gene of HBV genome were identified by using samples from the cohort. The mutation in hepatitis B virus (HBV) basal core promoter region of HBV genome has an accumulative effect on the occurrence of PLC. In addition, the tripartite relationship of aflatoxin exposure, P53 mutation and PLC was also investigated. Dynamic prediction model for PLC risk by using its long-term follow-up information and serial blood samples for QBC was developed. This model is expected to improve the efficiency of PLC screening in HBV infection individuals.

Entities:  

Keywords:  Prospective cohort; hepatitis B virus; primary liver cancer

Year:  2018        PMID: 29479565      PMCID: PMC5824723          DOI: 10.20517/2394-5079.2017.50

Source DB:  PubMed          Journal:  Hepatoma Res        ISSN: 2394-5079


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Authors:  G S Qian; R K Ross; M C Yu; J M Yuan; Y T Gao; B E Henderson; G N Wogan; J D Groopman
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  1994 Jan-Feb       Impact factor: 4.254

9.  Novel approach to identifying the hepatitis B virus pre-S deletions associated with hepatocellular carcinoma.

Authors:  Zhi-Mei Zhao; Yan Jin; Yu Gan; Yu Zhu; Tao-Yang Chen; Jin-Bing Wang; Yan Sun; Zhi-Gang Cao; Geng-Sun Qian; Hong Tu
Journal:  World J Gastroenterol       Date:  2014-10-07       Impact factor: 5.742

10.  Novel natural mutations in the hepatitis B virus reverse transcriptase domain associated with hepatocellular carcinoma.

Authors:  Yan Wu; Yu Gan; Fumin Gao; Zhimei Zhao; Yan Jin; Yu Zhu; Zhihan Sun; Hao Wu; Taoyang Chen; Jinbing Wang; Yan Sun; Chunsun Fan; Yongbing Xiang; Gengsun Qian; John D Groopman; Jianren Gu; Hong Tu
Journal:  PLoS One       Date:  2014-05-01       Impact factor: 3.240

View more
  1 in total

Review 1.  Mechanisms underlying aflatoxin-associated mutagenesis - Implications in carcinogenesis.

Authors:  Amanda K McCullough; R Stephen Lloyd
Journal:  DNA Repair (Amst)       Date:  2019-03-07
  1 in total

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