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质子泵抑制剂和组胺 2 受体拮抗剂与胰腺癌风险:一项巢式病例对照研究。

Proton pump inhibitors and histamine-2-receptor antagonists and pancreatic cancer risk: a nested case-control study.

机构信息

Clinical and Practice Research Group, School of Pharmacy, Queen's University Belfast, 97 Lisburn Road, Belfast, Northern Ireland BT9 7BL, UK.

出版信息

Br J Cancer. 2012 Jan 3;106(1):233-9. doi: 10.1038/bjc.2011.511. Epub 2011 Nov 22.

Abstract

BACKGROUND

The relationship between use of proton pump inhibitors (PPIs) and histamine-2-receptor antagonists (H(2)RAs) and pancreatic cancer risk has yet to be examined. Data from a range of studies suggest biologically plausible mechanisms, whereby these drugs (or the conditions for which they are prescribed) may affect pancreatic cancer risk. The objective of this study was to investigate the relationship between use of PPIs/H(2)RAs and pancreatic cancer risk.

METHODS

A nested case-control study was conducted within the UK general practice research database (GPRD). Cases had a diagnosis of exocrine pancreatic cancer and controls were matched to cases on general practice site, sex and year of birth. Exposure to PPIs and to H(2)RAs since entry into GPRD until 2 years before the diagnosis date (corresponding date in controls) and in the 5 years before the diagnosis date were separately assessed. Conditional logistic regression analyses were used to generate odds ratios (ORs) and 95% confidence intervals (CIs) associated with PPI or H(2)RA use compared with nonuse.

RESULTS

Ever use of PPIs since entry into the GPRD (excluding the 2 years prior to diagnosis) was not associated with risk of pancreatic cancer; OR (95% CI) 1.02 (0.85-1.22). Neither the dose nor the duration of PPI or H(2)RA use was associated with pancreatic cancer risk. No consistent patterns of association were seen when cumulative exposure (dose and duration) to these drugs was examined separately or together.

CONCLUSION

PPI/H(2)RA use, in a UK population, was not associated with pancreatic cancer risk.

摘要

背景

质子泵抑制剂 (PPIs) 和组胺 2 受体拮抗剂 (H₂RAs) 的使用与胰腺癌风险之间的关系尚未得到检验。来自一系列研究的数据表明存在生物学上合理的机制,这些药物(或其规定的用途)可能会影响胰腺癌的风险。本研究的目的是调查 PPI/H₂RA 使用与胰腺癌风险之间的关系。

方法

在英国一般实践研究数据库 (GPRD) 中进行了嵌套病例对照研究。病例组有外分泌胰腺癌症的诊断,对照组与病例组在一般实践地点、性别和出生日期上相匹配。分别评估了进入 GPRD 后至诊断日期前 2 年(对照组相应日期)以及诊断日期前 5 年内使用 PPI 和 H₂RA 的情况。采用条件逻辑回归分析生成与 PPI 或 H₂RA 使用相关的比值比 (OR) 和 95%置信区间 (CI),与未使用相比。

结果

进入 GPRD 后(不包括诊断前 2 年),PPIs 的使用与胰腺癌风险无关;OR(95%CI)为 1.02(0.85-1.22)。PPI 或 H₂RA 的剂量或使用时间均与胰腺癌风险无关。当分别或一起检查这些药物的累积暴露(剂量和时间)时,没有观察到一致的关联模式。

结论

在英国人群中,PPI/H₂RA 的使用与胰腺癌风险无关。

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