Vitamin D receptor gene variants and esophageal adenocarcinoma risk: A population-based case-control study

C.K. Chang, P.D. Thompson, H.G. Mulholland, M.M. Cantwell, L.A. Anderson, A.J. McKnight, L.J. Murray, B.T. Johnston, R.G.P. Watson, Helen Coleman

Research output: Contribution to journalArticlepeer-review

21 Citations (Scopus)


Purpose: Polymorphisms in the vitamin D receptor (VDR) gene may be of etiological importance in determining cancer risk. The aim of this study was to assess the association between common VDR gene polymorphisms and esophageal adenocarcinoma (EAC) risk in an all-Ireland population-based case-control study. Methods: EAC cases and frequency-matched controls by age and gender recruited between March 2002 and December 2004 throughout Ireland were included. Participants were interviewed, and a blood sample collected for DNA extraction. Twenty-seven single nucleotide polymorphisms in the VDR gene were genotyped using Sequenom or TaqMan assays while the poly(A) microsatellite was genotyped by fluorescent fragment analysis. Unconditional logistic regression was applied to assess the association between VDR polymorphisms and EAC risk. Results: A total of 224 cases of EAC and 256 controls were involved in analyses. After adjustment for potential confounders, TT homozygotes at rs2238139 and rs2107301 had significantly reduced risks of EAC compared with CC homozygotes. In contrast, SS alleles of the poly(A) microsatellite had significantly elevated risks of EAC compared with SL/LL alleles. However, following permutation analyses to adjust for multiple comparisons, no significant associations were observed between any VDR gene polymorphism and EAC risk. Conclusions: VDR gene polymorphisms were not significantly associated with EAC development in this Irish population. Confirmation is required from larger studies.
Original languageEnglish
Pages (from-to)512-517
Number of pages6
JournalJournal of gastrointestinal cancer
Issue number3
Publication statusPublished - 01 Sept 2012


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