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Acid-suppressing therapies and subsite-specific risk of stomach cancer

BACKGROUND: Associations of stomach cancer risk with histamine type-2 receptor antagonists (H(2)RA) and proton-pump inhibitors (PPI) are controversial. We hypothesised that proximal extension of Helicobacter pylori infection from acid suppression would disproportionately increase cancers at proximal...

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Detalles Bibliográficos
Autores principales: Wennerström, E Christina M, Simonsen, Jacob, Camargo, M Constanza, Rabkin, Charles S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418456/
https://www.ncbi.nlm.nih.gov/pubmed/28350791
http://dx.doi.org/10.1038/bjc.2017.84
Descripción
Sumario:BACKGROUND: Associations of stomach cancer risk with histamine type-2 receptor antagonists (H(2)RA) and proton-pump inhibitors (PPI) are controversial. We hypothesised that proximal extension of Helicobacter pylori infection from acid suppression would disproportionately increase cancers at proximal subsites. METHODS: A total of 1 563 860 individuals in the Danish Prescription Drug Registry first prescribed acid-suppressive drugs 1995–2011 were matched to unexposed population-based controls. Hazard ratios (HR) were calculated by Cox proportional hazard regression for stomach cancers diagnosed more than one year after first prescription. RESULTS: There were 703 stomach cancers among H(2)RA-exposed individuals and 1347 among PPI-exposed. Restricted to individuals with five or more prescriptions, subsite-specific HRs for H(2)RA and PPI were 4.1 and 6.4 for proximal subsites vs 8.0 and 10.3 for distal subsites, respectively. CONCLUSIONS: Moderate exposures to acid-suppressive drugs did not favour proximal tumour localisation. Given confounding by indication, these findings do not resolve potential contribution to gastric carcinogenesis overall.