Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2006 Nov;55(11):1538-44.
doi: 10.1136/gut.2005.086579. Epub 2006 Jun 19.

Gastric acid suppression and risk of oesophageal and gastric adenocarcinoma: a nested case control study in the UK

Affiliations

Gastric acid suppression and risk of oesophageal and gastric adenocarcinoma: a nested case control study in the UK

L A García Rodríguez et al. Gut. 2006 Nov.

Abstract

Background: Gastric acid suppressing drugs (that is, histamine(2) receptor antagonists and proton pump inhibitors) could affect the risk of oesophageal or gastric adenocarcinoma but few studies are available.

Aims: To study the association between long term treatment with acid suppressing drugs and the risk of oesophageal or gastric adenocarcinoma.

Patients: Persons registered in the general practitioners research database in the UK and aged 40-84 years during the period 1994-2001.

Methods: Population based nested case control study. Multivariable unconditional logistic regression was used to calculate odds ratios (ORs) with 95% confidence intervals (CI).

Results: In 4 340 207 person years of follow up, 287 patients with oesophageal adenocarcinoma, 195 with gastric cardia adenocarcinoma, and 327 with gastric non-cardia adenocarcinoma were identified, and 10 000 control persons were randomly sampled. "Oesophageal" indication for long term acid suppression (that is, reflux symptoms, oesophagitis, Barrett's oesophagus, or hiatal hernia) rendered a fivefold increased risk of oesophageal adenocarcinoma (odds ratio (OR) 5.42 (95% confidence interval (CI) 3.13-9.39)) while no association was observed among users with a group of other indications, including peptic ulcer and "gastroduodenal symptoms" (that is, gastritis, dyspepsia, indigestion, and epigastric pain) (OR 1.74 (95% CI 0.90-3.34)). "Peptic ulcer" indication (that is, gastric ulcer, duodenal ulcer, or unspecified peptic ulcer) was associated with a greater than fourfold increased risk of gastric non-cardia adenocarcinoma among long term users (OR 4.66 (95% CI 2.42-8.97)) but no such association was found in those treated for a group of other indications (that is, "oesophageal" or "gastroduodenal symptoms") (OR 1.18 (95% CI 0.60-2.32)).

Conclusions: Long term pharmacological gastric acid suppression is a marker of increased risk of oesophageal and gastric adenocarcinoma. However, these associations are most likely explained by the underlying treatment indication being a risk factor for the cancer rather than an independent harmful effect of these agents per se.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest: None declared.

Comment in

References

    1. Devesa S S, Blot W J, Fraumeni J F., Jr Changing patterns in the incidence of esophageal and gastric carcinoma in the United States. Cancer 1998832049–2053. - PubMed
    1. Bollschweiler E, Wolfgarten E, Gutschow C.et al Demographic variations in the rising incidence of esophageal adenocarcinoma in white males. Cancer 200192549–555. - PubMed
    1. Hansson L E, Sparen P, Nyren O. Increasing incidence of both major histological types of esophageal carcinomas among men in Sweden. Int J Cancer 199354402–407. - PubMed
    1. Parkin D M. Global cancer statistics in the year 2000. Lancet Oncol 20012533–543. - PubMed
    1. Enzinger P C, Mayer R J. Esophageal cancer. N Engl J Med 20033492241–2252. - PubMed

Publication types

MeSH terms