NOD2/CARD15 gene polymorphisms are not associated with collagenous colitis.

Abstract:

BACKGROUND:Collagenous colitis is a chronic inflammatory bowel disease of unknown origin. In some cases of collagenous colitis, histomorphological features are comparable to other inflammatory bowel diseases. AIM:To assess functional NOD2/CARD15 polymorphisms for the susceptibility to collagenous colitis in a case-control study. MATERIALS AND METHODS:Seventy-five patients with symptomatic collagenous colitis and 534 healthy blood donors were genotyped for SNP 8, 12, and 13 of the NOD2/CARD15 gene using TaqMan technology. Susceptibility to collagenous colitis was tested using Chi(2)-test comparing the carrier status of the rare allele. RESULTS:The carrier frequency of the rare allele in SNP 8, 12, and 13 was 9.5, 1.3, and 8.1% in patients with collagenous colitis and 8.9, 1.1, and 8.4% in healthy blood donors, respectively. There were no significant differences in allele-, genotype, and carrier frequency (p>0.05). CONCLUSION:Our data suggest that functional polymorphisms in the NOD2/CARD15 gene might not be involved in the susceptibility to collagenous colitis.

journal_name

Int J Colorectal Dis

authors

Madisch A,Hellmig S,Schreiber S,Bethke B,Stolte M,Miehlke S

doi

10.1007/s00384-006-0158-x

subject

Has Abstract

pub_date

2007-04-01 00:00:00

pages

425-8

issue

4

eissn

0179-1958

issn

1432-1262

journal_volume

22

pub_type

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