Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Hepatology. 2019 Mar;69(3):1151-1164. doi: 10.1002/hep.30247. Epub 2019 Feb 7.
Researchers have hypothesized that the long-term use of proton pump inhibitors (PPIs) can increase the risk of developing cancer. However, the association between PPI use and hepatocellular carcinoma (HCC) risk is unclear. Using data from the Taiwan National Health Insurance Research Database for the period between 2003 and 2013, we identified 35,356 patients with chronic hepatitis B virus (HBV) or hepatitis C virus (HCV) infections. One-to-one propensity score matching by gender, age, cohort entry year, comorbidity, and medication resulted in the inclusion of 7,492 pairs of patients (PPI users and non-PPI users) for analyses. We performed multivariate and stratified analysis using the Kaplan-Meier method and Cox proportional hazards models in order to estimate the association between PPI use and the risk of developing HCC. In the HBV cohort, 237 patients developed HCC during a median follow-up of 53 months. However, PPI use was not associated with an increased risk of developing HCC (adjusted hazard ratio [aHR], 1.25; 95% confidence interval [CI], 0.90-1.73; P = 0.18). In the HCV cohort, 211 patients developed HCC; but again, PPI use was not associated with an increase in the risk of developing HCC (aHR, 1.19; 95% CI, 0.88-1.61; P = 0.25). We observed no relationship between a dose-dependent effect of PPI use and HCC risk. Subgroup analysis also confirmed that PPI use was not correlated to an increased HCC risk. Conclusion: Based on a retrospective population-based cohort study throughout Taiwan, where the prescription of PPI is tightly regulated, PPI use is not associated with the risk of developing HCC among patients with chronic HBV or HCV infections.
研究人员假设质子泵抑制剂 (PPI) 的长期使用会增加患癌症的风险。然而,PPI 使用与肝细胞癌 (HCC) 风险之间的关联尚不清楚。我们使用 2003 年至 2013 年期间台湾全民健康保险研究数据库的数据,确定了 35356 例慢性乙型肝炎病毒 (HBV) 或丙型肝炎病毒 (HCV) 感染患者。通过性别、年龄、队列进入年份、合并症和药物进行 1:1 倾向评分匹配,共纳入 7492 对患者(PPI 使用者和非 PPI 使用者)进行分析。我们使用 Kaplan-Meier 方法和 Cox 比例风险模型进行多变量和分层分析,以估计 PPI 使用与 HCC 发展风险之间的关联。在 HBV 队列中,237 例患者在中位随访 53 个月期间发生 HCC。然而,PPI 使用与 HCC 发展风险增加无关(调整后的危险比 [aHR],1.25;95%置信区间 [CI],0.90-1.73;P = 0.18)。在 HCV 队列中,211 例患者发生 HCC;但是,PPI 使用与 HCC 发展风险增加无关(aHR,1.19;95%CI,0.88-1.61;P = 0.25)。我们没有观察到 PPI 使用剂量依赖性与 HCC 风险之间的关系。亚组分析也证实 PPI 使用与 HCC 风险增加无关。结论:基于台湾一项回顾性基于人群的队列研究,在台湾,PPI 的处方受到严格监管,PPI 使用与慢性 HBV 或 HCV 感染患者 HCC 风险增加无关。