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  • Author: Andersen, Vibeke

    Viborg Regional Hospital

  • Author: Ernst, Anja

    Aalborg University Hospital

  • Author: Sventoraityte, Jurgita

    Lithuanian University of Health Sciences

  • Author: Kupcinskas, Limas

    Lithuanian University of Health Sciences

  • Author: Jacobsen, Bent A.

    Aalborg University Hospital

  • Author: Krarup, Henrik B.

    Aalborg University Hospital

  • Author: Vogel, Ulla Birgitte

    Department of Micro- and Nanotechnology, Technical University of Denmark

  • Author: Jonaitis, Laimas

    Lithuanian University of Health Sciences

  • Author: Denapiene, Goda

    Vilnius University

  • Author: Kiudelis, Gediminas

    Lithuanian University of Health Sciences

  • Author: Balschun, Tobias

    Christian-Albrechts University, Germany

  • Author: Franke, Andre

    Christian-Albrechts University, Germany

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Background: Differences in the genetic architecture of inflammatory bowel disease between different European countries and ethnicities have previously been reported. In the present study, we wanted to assess the role of 11 newly identified UC risk variants, derived from a recent European UC genome wide association study (GWAS) (Franke et al., 2010), for 1) association with UC in the Nordic countries, 2) for population heterogeneity between the Nordic countries and the rest of Europe, and, 3) eventually, to drive some of the previous findings towards overall genome-wide significance. Methods: Eleven SNPs were replicated in a Danish sample consisting of 560 UC patients and 796 controls and nine missing SNPs of the German GWAS study were successfully genotyped in the Baltic sample comprising 441 UC cases and 1156 controls. The independent replication data was then jointly analysed with the original data and systematic comparisons of the findings between ethnicities were made. Pearson's chi(2), Breslow-Day (BD) and Cochran-Mantel-Haenszel (CMH) tests were used for association analyses and heterogeneity testing. Results: The rs5771069 (IL17REL) SNP was not associated with UC in the Danish panel. The rs5771069 (IL17REL) SNP was significantly associated with UC in the combined Baltic, Danish and Norwegian UC study sample driven by the Norwegian panel (OR = 0.89, 95% CI: 0.79-0.98, P = 0.02). No association was found between rs7809799 (SMURF1/KPNA7) and UC (OR = 1.20, 95% CI: 0.95-1.52, P = 0.10) or between UC and all other remaining SNPs. We had 94% chance of detecting an association for rs7809799 (SMURF1/KPNA7) in the combined replication sample, whereas the power were 55% or lower for the remaining SNPs. Statistically significant PBD was found for OR heterogeneity between the combined Baltic, Danish, and Norwegian panel versus the combined German, British, Belgian, and Greek panel (rs7520292 (P = 0.001), rs12518307 (P = 0.007), and rs2395609 (TCP11) (P = 0.01), respectively). No SNP reached genome-wide significance in the combined analyses of all the panels. Conclusions: This replication study supports an important role for the studied rs5771069 (IL17REL) SNP, but not for rs7809799 (SMURF1/KPNA7), in UC etiology in the Danish, Baltic, and Norwegian populations. Significant genetic heterogeneity was suggested for rs7520292, rs12518307, and rs2395609 (TCP11) in UC etiology between the Nordic and the other European populations.
Original languageEnglish
JournalB M C Medical Genetics
Publication date2011
Volume12
Issue139
ISSN1471-2350
DOIs
StatePublished
CitationsWeb of Science® Times Cited: 3
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