The relation between NOD2/CARD15 mutations and the prevalence and phenotypic heterogeneity of Crohn's disease: Lessons from the Israeli Arab Crohn's disease cohort

Amir Karban*, Oren Atia, Eran Leitersdorf, Azmi Shahbari, Wisam Sbeit, Zvi Ackerman, Rawia Mualem, Arie Levine, Shula Nesher, Rifaat Safadi, Rami Eliakim

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

The prevalence of Crohn's disease depends on geographic location and racial background. Arg702Trp, Gly908Arg, and Leu1007fsinsC mutations in the NOD2/CARD15 gene are associated with Crohn's disease in Caucasians. The mutation rate among Israeli Jewish patients is 27%-41%. The prevalence of Crohn's disease is much lower in the Israeli Arab compared to the Israeli Jewish population. We studied the NOD2/CARD15 mutation rate and disease phenotype (according to the Vienna classification) among the Israeli Arabs and compared them with those in an Israeli Jewish cohort. We recruited 66 Israeli Arab patients and 122 ethnically matched controls. Five patients (8.2%) and three controls (2.3%) carried one NOD2/CARD15 mutation. The phenotypic characteristics of the Arab and Jewish patients were very similar. We conclude that NOD2/CARD15 mutations do not contribute to Crohn's susceptibility in the Israeli Arab population and suggest that NOD2/CARD15 mutations have an important effect on Crohn's prevalence within a specific population but not on the phenotype.

Original languageEnglish
Pages (from-to)1692-1697
Number of pages6
JournalDigestive Diseases and Sciences
Volume50
Issue number9
DOIs
StatePublished - Sep 2005
Externally publishedYes

Funding

Funders
American Society for Technion
British Friends of Rambam Medical Center
Technion Israel Institute of Technology

    Keywords

    • Arabs
    • Crohn's disease
    • Genetics
    • Israel
    • NOD2/CARD15

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