Annals of Oncology Advance Access published online on March 27, 2008
Annals of Oncology, doi:10.1093/annonc/mdn055
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Analysis of Pro12Ala PPAR gamma polymorphism and Helicobacter pylori infection in gastric adenocarcinoma and peptic ulcer disease
1 Department of Microbiology
2 Department of Gastroenterology
3 Department of Pathology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow
4 Department of Gastroenterology, Central Command Hospital, Lucknow, India
* Correspondence to: Dr K. N. Prasad, Department of Microbiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow 226 014, India. Tel: +91-522-2668631; Fax: +91-522-2668017; E-mail: knprasad{at}sgpgi.ac.in
Background: Peroxisome proliferator-activated receptor gamma (PPAR
) is a ligand-dependent transcription factor involved in various disease processes including inflammation and carcinogenesis. We investigated the association of Pro12Ala PPAR
polymorphism and Helicobacter pylori infection with gastric cancer and peptic ulcer disease (PUD).
Patients and methods: In total, 348 adult patients [62 gastric adenocarcinoma, 45 PUD and 241 nonulcer dyspepsia (NUD)] who underwent an upper gastrointestinal endoscopy were enrolled. PPAR
polymorphism was analyzed by PCR-based restriction fragment length polymorphism. H. pylori infection was diagnosed by rapid urease test, culture, histopathology and PCR.
Results: PPAR
G carrier had significant association with gastric adenocarcinoma [P = 0.023, odds ratio (OR) = 2.136, 95% CI = 1.112–4.104] and PUD (P = 0.028, OR = 2.165, 95% CI = 1.008–4.306) when compared with NUD. Combination of G carrier and H. pylori infection further increased the risk of gastric adenocarcinoma (OR = 3.054, 95% CI = 1.195–7.807) and PUD (OR = 11.161, 95% CI = 3.495–35.644). PPAR
polymorphism did not increase the risk of gastric adenocarcinoma and PUD in H. pylori-negative subjects.
Conclusions: The study suggests that Pro12Ala PPAR
polymorphism is associated with gastric adenocarcinoma and PUD, and is a potential marker for genetic susceptibility to these two diseases in the presence of H. pylori infection.
gastric adenocarcinoma, Helicobacter pylori infection, peptic ulcer disease, PPAR
polymorphism
Received for publication January 4, 2008. Revision received February 3, 2008. Accepted for publication February 4, 2008.