Crohn's disease is a disease of complex etiology, multifactorial and still poorly understood. This disease, due to its morbidity and mortality, poses a significant public health problem in France. Apart from the involvement of bacterial factors and those involving the permeability of the epithelial barrier, it is now well recognized that several factors are associated with genetic predisposition in some of these patients. Among these factors, the Nod2 mutations were first identified. Studies concerning the presence of these mutations and the severity of disease results were sometimes conflicting. Very recently, new interesting mutations in genes involved in autophagy were found with greater frequency in patients with Crohn's disease. These mutations observed in Atg16 and IRGM genes. It has been particularly shown on large patient cohorts,the IRGM polymorphism was associated with a progressive disease, with histological severity scores. One of the severity criteria of Crohn's disease is the early recurrence observed in some patients after surgical resection of the injured segment. Predictive factors for such recurrence after surgery are not known or not.
Study Type
OBSERVATIONAL
Enrollment
230
CHU de Grenoble
Grenoble, France
AP-HM
Marseille, France
CHU de Montpellier
Montpellier, France
CHU de Nice
Nice, France
Search for IRGM mutations and compare the frequency of these mutations.
Patients who receive surgical resection for intestinal MC have, within six months after surgery gastrointestinal endoscopy for judging the endoscopic recurrence and modify treatment if necessary. This quantifies the endoscopic recurrence of i0 to i4 classified according to the Rutgeerts score (45). Patients who have a score ≥ i2 have a severe endoscopic recurrence. We will compare the prevalence of sick with a score ≥ i2 in patient groups with or without mutation in the gene IRGM. The investigators will look for the existence of a mutation in the gene IRGM, Atg16 and IL23R. The mutation in the gene IRGM being the main prognostic factor, mutations in the genes IL23R Atg16 and prognostic factors constituting secondary.
Time frame: 6 months post surgery
To assess the prevalence of mutations IGRM in a prospective series of 200 patients operated
The prevalence of mutations IGRM, Atg16 and IL23 will be determined
Time frame: 6 months post surgery
Determine whether there are phenotypic characteristics of the disease associated with mutations of IGRM
The investigators will compare the frequency of postoperative recurrence in patients who have a mutation in the genes IL23 and Atg16
Time frame: 6 months post surgery
Determine whether there are pathological features associated with mutations of IGRM.
The investigators will determine if the main phenotypic characteristics of CD (age of onset, time between diagnosis and surgery, use of immunosuppressive and biologic therapies, smoking localization of the disease, etc..) Are associated with increased prevalence of mutations of IGRM, Atg16 and IL23R.
Time frame: 6 months post surgery
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