Article
Vitamin D receptor gene polymorphism: association with Crohn's
disease susceptibility
J D Simmonsa, C Mullighanb, K I Welshb, D P Jewella
a Gastroenterology
Unit, University of Oxford, Radcliffe Infirmary, Woodstock Rd, Oxford,
OX2 6HE, UK, b Transplant Immunology, Transplant Centre,
Churchill Hospital, Oxford, UK
Correspondence to: J D Simmons, Gastroenterology Unit, John Radcliffe Hospital, Oxford, OX3 9DU, UK. Email: jonsimmons{at}doctors.org.uk
Accepted for publication 8 February 2000
BACKGROUND
The vitamin
D receptor (VDR) gene represents a strong positional candidate
susceptibility gene for inflammatory bowel disease (IBD). The VDR gene
maps to a region on chromosome 12 that has been shown to be linked to
IBD by genome screening techniques. It is the cellular receptor for
1,25(OH)2 vitamin D3 (calcitriol) which has a
wide range of different regulatory effects on the immune system. IBD is
characterised by activation of the mucosal immune system.
AIM
To determine if
polymorphisms in the VDR gene are associated with susceptibility to IBD
SUBJECTS
European
Caucasoids: 158 patients with ulcerative colitis, 245 with Crohn's
disease, and 164 cadaveric renal allograft donor controls.
METHOD
Single
nucleotide polymorphisms (TaqI,
ApaI, and FokI)
in VDR were typed in patients with Crohn's disease, ulcerative
colitis, and controls by polymerase chain reaction with sequence
specific primers.
RESULTS
There were
significantly more homozygotes for the TaqI
polymorphism at codon 352 of exon 8 (genotype
"tt") among patients with Crohn's
disease (frequency 0.22) than patients with ulcerative colitis (0.12)
or controls (0.12) (odds ratio 1.99; 95% confidence interval
1.14-3.47; p=0.017).
CONCLUSION
This study
provides preliminary evidence for a genetic association between
Crohn's disease susceptibility and a gene that lies within one of the
candidate regions determined by linkage analysis.
Keywords: inflammatory bowel disease; genetics; candidate genes; vitamin D
© 2000 by Gut
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