Medical College of Wisconsin
CTSIResearch InformaticsREDCap

Molecular stratification of Crohn's disease by chemokine receptors: fractalkine receptor polymorphisms define a fibrostenosing ileal subgroup. Am J Gastroenterol 2006 Jan;101(1):107-9

Date

01/13/2006

Pubmed ID

16405541

DOI

10.1111/j.1572-0241.2006.00357.x

Scopus ID

2-s2.0-33644850652 (requires institutional sign-in at Scopus site)   2 Citations

Abstract

The association of NOD2/CARD15 gene mutations with Crohn's disease (CD) has also provided proof of principle that anatomic location (ileal disease) and stricturing behavior is associated with specific genetic variants. However, the majority of CD patients of Caucasian descent, and essentially all minority CD patients do not possess NOD2/CARD15 mutations. Although these early lessons from NOD2/CARD15 genotype/phenotype correlations are encouraging, much more needs to be done to adequately understand the CD spectrum of subgroups. The study by Brand et al. demonstrates that a chemokine receptor polymorphism (CX3CR1 T280) can also influence disease location and behavior, suggesting yet another genetic variant that can help to subgroup CD patients. Findings similar to the study by Brand and colleagues in this issue of American Journal of Gastroenterology suggest that panels of susceptibility alleles and polymorphisms will ultimately allow an early genetic determination that will correspond with unique clinical patterns of CD: increased expression of the chemokine fractalkine in Crohn's disease and association of the factalkine receptor T280M polymorphism with a fibrostenosing disease phenotype.

Author List

Binion DG, Kugathasan S, Dwinell MB

Author

Michael B. Dwinell PhD Center Director, Professor in the Microbiology and Immunology department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

CX3C Chemokine Receptor 1
Crohn Disease
Female
Genetic Markers
Genetic Predisposition to Disease
Humans
Ileal Diseases
Intestinal Mucosa
Intestinal Obstruction
Male
Phenotype
Polymorphism, Genetic
Prognosis
Receptors, Chemokine
Receptors, Cytokine
Receptors, HIV
Risk Assessment
Severity of Illness Index