Tamim Hani, Duranceau André, Chen Long-Qi, Lelorier Jacques
Pharmacoepidemiology and Pharmacoeconomics Unit, University of Montreal Hospital Center/Hôtel-Dieu Hospital, Montreal, Quebec, Canada.
Drug Saf. 2008;31(8):675-84. doi: 10.2165/00002018-200831080-00004.
The risk of gastric cancer could be influenced by acid-related diseases or by the use of acid-suppressive drugs, such as histamine H(2) receptor antagonists and proton pump inhibitors (PPIs).
To assess the association between exposure to acid-suppressive drugs and the risk of gastric cancer.
A nested case-control study was conducted among people registered in the Quebec health insurance plan (Canada). Cases represented a random sample of subjects diagnosed with gastric cancer between 1995 and 2003 who were matched on age and sex to at least four controls (using incidence density sampling). The index date was the date of cancer diagnosis for the cases, which was the index date for the matched controls. The exposure definition in the 5 years preceding the index date was based on the defined daily doses of acid-suppressive drugs and categorized into quartiles.
The study included 1598 gastric cancer cases and 12 991 controls. The adjusted odds ratios for the association between exposure to acid-suppressive drugs and risk of gastric cancer were 1.47 (95% CI 1.23, 1.76), 1.32 (95% CI 1.10, 1.58), 1.48 (95% CI 1.24, 1.77) and 1.18 (95% CI 0.97, 1.44) for the first, second, third and fourth exposure quartiles, respectively. Similar results were obtained when use of H(2) receptor antagonists and PPIs were assessed separately (odds ratios for the association between PPIs and the risk of gastric cancer were slightly higher compared with H(2) receptor antagonists and risk of gastric cancer).
A minor increase in the risk of gastric cancer was observed if exposure to either H(2) receptor antagonists or PPIs occurred within the past 5 years. However, this association is probably not causal since it is most likely due to confounding by indication.
胃癌风险可能受酸相关疾病或抑酸药物使用的影响,如组胺H2受体拮抗剂和质子泵抑制剂(PPIs)。
评估接触抑酸药物与胃癌风险之间的关联。
在加拿大魁北克医疗保险计划登记的人群中进行了一项巢式病例对照研究。病例为1995年至2003年间被诊断为胃癌的随机样本,按年龄和性别与至少四个对照匹配(采用发病密度抽样)。索引日期为病例的癌症诊断日期,也是匹配对照的索引日期。索引日期前5年的暴露定义基于抑酸药物的限定日剂量,并分为四分位数。
该研究纳入了1598例胃癌病例和12991例对照。接触抑酸药物与胃癌风险之间关联的校正比值比,第一、第二、第三和第四暴露四分位数分别为1.47(95%CI 1.23,1.76)、1.32(95%CI 1.10,1.58)、1.48(95%CI 1.24,1.77)和1.18(95%CI 0.97,1.44)。分别评估H2受体拮抗剂和PPIs的使用时,得到了类似结果(与H2受体拮抗剂和胃癌风险相比,PPIs与胃癌风险之间关联的比值比略高)。
如果在过去5年内接触过H2受体拮抗剂或PPIs,胃癌风险会有轻微增加。然而,这种关联可能不是因果关系,因为很可能是由指征混杂所致。