Hepatitis B or C viral infection and risk of pancreatic cancer: A meta-analysis of observational studies

被引:55
|
作者
Xu, Jian-Hua [1 ,2 ,3 ,4 ]
Fu, Jin-Jian [1 ,5 ]
Wang, Xiao-Li [2 ]
Zhu, Jia-Yong [3 ]
Ye, Xiao-Hua [2 ]
Chen, Si-Dong [2 ]
机构
[1] Southern Med Univ, Sch Publ Hlth & Trop Med, Dept Pathogen Biol, Guangzhou 510515, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Sch Publ Hlth, Guangdong Key Lab Mol Epidemiol, Guangzhou 510006, Guangdong, Peoples R China
[3] Guangdong Pharmaceut Univ, Inst Pharmaceut Bioact Subst Res, Guangzhou 510006, Guangdong, Peoples R China
[4] Guangdong Prov Hosp Chinese Med, Dept Clin Lab, Guangzhou 510120, Guangdong, Peoples R China
[5] Liuzhou Municipal Matern & Child Healthcare Hosp, Liuzhou 545001, Guangxi Provinc, Peoples R China
关键词
Hepatitis B; Hepatitis C; Pancreatic cancer; Observational studies; Meta-analysis; VIRUS-INFECTION; EPIDEMIOLOGY; REPLICATION; ASSOCIATION; DNA;
D O I
10.3748/wjg.v19.i26.4234
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate if there is an association between hepatitis B virus (HBV) or hepatitis C virus (HCV) infection and the risk of pancreatic cancer. METHODS: All relevant studies published before 11 October, 2012 were identified by a systematic search of MEDLINE, EMBASE, BIOSIS Previews and the Cochrane Library databases and with cross-referencing. The observational studies that reported RR or OR estimates with 95% CIs for the association between HBV or HCV and pancreatic cancer were included. A random-effects model was used to summarize meta-analytic estimates. The Newcastle-Ottawa quality assessment scale was applied to assess the quality of the methodology in the included studies. RESULTS: A total of 8 eligible studies were selected for meta-analysis. Overall, chronic hepatitis B and inactive hepatitis B surface antigen (HBsAg) carrier state (HBsAg positive) had a significantly increased risk of pancreatic cancer with OR of 1.20 (95% CI: 1.01-1.39), especially in the Chinese population (OR = 1.30, 95% CI: 1.05-1.56). Past exposure to HBV (possible occult HBV infection) had an increased OR of pancreatic cancer risk (OR = 1.24, 95% CI: 1.05-1.42), especially among those patients without natural immunity [anti hepatitis B core (HBc) positive/hepatitis B surface antibody (anti HBs) negative], with OR of 1.67 (95% CI: 1.13-2.22). However, past exposure to HBV with natural immunity (anti-HBc positive/anti-HBs positive) had no association with pancreatic cancer development, with OR 0.98 (95% CI: 0.80-1.16), nor did the HBV active replication (hepatitis B e antigen positive status), with OR 0.98 (95% CI: 0.27-1.68). The risk of pancreatic cancer among anti-HBs positive patients was significantly lower than among anti-HBs negative patients (OR = 0.54, 95% CI: 0.46-0.62). Past exposure to HCV also resulted in an increased risk of pancreatic cancer (OR = 1.26, 95% CI: 1.03-1.50). Significant between-study heterogeneity was observed. Evidence of publication bias for HBV/HCV infection-pancreatic cancer association was not found. CONCLUSION: Chronic HBV and HCV infection increases pancreatic cancer risk. Our findings underscore the need for more studies to confirm this potential relationship. (C) 2013 Baishideng. All rights reserved.
引用
收藏
页码:4234 / 4241
页数:8
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