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Search: WFRF:(Pettersson Jonas) > (2005-2009) > CARD15/NOD2 polymor...

  • Halfvarson, Jonas,1970-Division of Gastroenterology, Department of Internal Medicine, Orebro University Hospital, Orebro, Sweden (author)

CARD15/NOD2 polymorphisms do not explain concordance of Crohn´s disease in Swedish monozygotic twins

  • Article/chapterEnglish2005

Publisher, publication year, extent ...

  • Elsevier BV,2005
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:oru-27391
  • https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-27391URI
  • https://doi.org/10.1016/j.dld.2005.05.005DOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:1953034URI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-33366URI

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  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • BACKGROUND: CARD15/NOD2 polymorphisms are associated with Crohn's disease. There is a high concordance for disease and disease phenotype in monozygotic twin pairs with Crohn's disease.AIM: We studied CARD15/NOD2 polymorphisms in a Swedish, population-based cohort of monozygotic twins with Crohn's disease to assess whether these variants explain disease concordance.SUBJECTS AND METHODS: Twenty-nine monozygotic twin pairs (concordant n=9, discordant n=20) with Crohn's disease and 192 healthy controls were investigated for the CARD15/NOD2 variants Arg702Trp, Gly908Arg and Leu1007fsinsC.RESULTS: CARD15/NOD2 mutations were found in 5/38 (13%) twins with Crohn's disease, corresponding to a total allele frequency of 6.6%. Only 2/9 concordant twin pairs carried any of the variants and the remaining seven were wild type genotype. The total allele frequency was 4.4 times higher (95% confidence interval 1.0-21.5, p=0.06) in concordant twins than in discordant ones, 11.1% versus 2.5%. In healthy controls the total allele frequency was 2.6%.CONCLUSIONS: CARD15/NOD2 polymorphisms contribute but do not alone explain concordance of Crohn's disease in monozygotic twins and, at least in a Swedish population, other polymorphisms are required. The low occurrence of CARD15/NOD2 mutations in the study and other Northern European populations suggests that these variants are of less importance in Northern Europe.

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  • Bresso, FKarolinska Institutet,IRIS Center, Karolinska Institute-MTC, Stockholm, Sweden (author)
  • D ´Amato, MKarolinska Institutet,IRIS Center, Karolinska Institute-MTC, Stockholm, Sweden (author)
  • Järnerot, GDivision of Gastroenterology, Department of Internal Medicine, Örebro University Hospital, Örebro, Sweden (author)
  • Pettersson, SKarolinska Institutet,IRIS Center, Karolinska Institute-MTC, Stockholm, Sweden (author)
  • Tysk, CDivision of Gastroenterology, Department of Internal Medicine, Örebro University Hospital, Örebro, Sweden (author)
  • Karolinska InstitutetDivision of Gastroenterology, Department of Internal Medicine, Orebro University Hospital, Orebro, Sweden (creator_code:org_t)

Related titles

  • In:Digestive and Liver Disease: Elsevier BV37:10, s. 768-7621590-86581878-3562

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