Helicobacter pylori infection, atrophic gastritis, and pancreatic cancer risk A meta-analysis of prospective epidemiologic studies

被引:21
作者
Liu, Hong [1 ]
Chen, Yue-Tong [2 ]
Wang, Rui [3 ]
Chen, Xin-Zu [4 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Integrated Tradit Chinese & Western Med, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Gastroenterol, Intens Care Unit, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Gastroenterol, Nursing Sect, Chengdu, Sichuan, Peoples R China
[4] Sichuan Univ, West China Hosp, Dept Gastrointestinal Surg, Guo Xue Xiang 37, Chengdu 610041, Sichuan, Peoples R China
基金
中央高校基本科研业务费专项资金资助; 中国国家自然科学基金;
关键词
atrophic gastritis; cytotoxin-associated gene A; epidemiology; Helicobacter pylori; pancreatic cancer; ASSOCIATION; POPULATION; CHINA; SEROPOSITIVITY; ANTIBODIES;
D O I
10.1097/MD.0000000000007811
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: To investigate the associations of Helicobacter pylori (Hp) infection and atrophic gastritis (AG) with pancreatic cancer risk. Methods: A literature search in PubMed was performed up to July 2017. Only prospective cohort and nested case-control studies enrolling cancer-free participants were eligible. Incident pancreatic cancer cases were ascertained during the follow-up. The risks of pancreatic cancer were compared between persons infected and noninfected with Hp, or between those with and without AG status at baseline. Odds ratios (ORs) or hazard ratios were combined. Subgroup and sensitivity analyses were performed, and publication bias was estimated. Results: Three cohort studies and 6 nested case-control studies, including 65,155 observations, were analyzed. The meta-analyses did not confirm the association between pancreatic cancer risk and Hp infection (OR=1.09, 95% confidence interval [CI]= 0.81-1.47) or AG status (OR=1.18, 95% CI=0.80-1.72). However, particular subpopulations potentially had increased risks of pancreatic cancer. Cytotoxin-associated gene A (CagA)-negative strains of Hp might be a causative factor of pancreatic cancer (OR=1.30, 95% CI=1.05-1.62), but a sensitivity analysis by leave-one-out method did not fully warrant it (OR=1.20, 95% CI= 0.93-1.56). In 1 nested case-control study, AG at stomach corpus in Hp-negative subpopulation might have increased risk of pancreatic cancer, but with a poor test power=0.56. Publication biases were nonsignificant in the present meta-analysis. Conclusion: Based on current prospective epidemiologic studies, the linkage of pancreatic cancer to Hp infection or AG status was not warranted on the whole. Nevertheless, prospective studies only focusing on those specific subpopulations are further required to obtain better power.
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页数:8
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