Crohn Disease
Conditions
Keywords
genetic
Brief summary
This study highlight genetics mutations with major effect in Crohn's Disease (CD) by WES in individuals affected and healthy individuals from EPIMAD Inserm InVS registry families.
Detailed description
The EPIMAD Registry covers a large area of Northern France (9 millions inhabitants) and collects all incident CD cases and data from CD multiplex families (families with 3 or more CD affected patients) in the Nord the Pas de Calais the Somme and the Seine Maritime. If the investigators could demonstrate that most CD cases from multiplex families were related to high frequency of NOD2 gene mutations, the investigators found some CD multiplex families without any NOD2 gene involvement. Thus in these families high prevalence of CD cases may rely on other major genetic susceptibility variant(s) that remain to be determined. this clinical research Whole Exome Sequencing protocol, aiming to highlight genetics mutations with major effect in CD has been initiated. This study is a familial genetic study with intra-familial controls. The genetics analyses are: * Ascertain of no significant NOD2 mutation in the family members by Sanger DNA sequencing * WES (CD patients and family controls unaffected subjects) * Genotyping of all mutations found, case control and segregation analyses to validate their implication in CD.
Interventions
GENETICgenetic analysis
genetic (Whole Exome Sequencing )
BIOLOGICALblood and stools samples
biological collection
Sponsors
University Hospital, Lille
Study design
Observational model
FAMILY_BASED
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
5 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Crohn disease subject * EPIMAD family with, at least, 3 Crohn disease subjects
Exclusion criteria
* Pregnant or lactating women
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| NOD2 gene status | 8 months after recruiting | One of the main inclusion criteria is the absence in the family (and thus in the proband) of any NOD2 mutation that could be related with the high occurrence of Crohn's Disease in the family. So verification of the lack of CD related NOD2 gene mutation is a prerequisite to the inclusion of the family in the protocol. This is achieved by Sanger sequencing of all exons, exon-intron junctions and search for already described intronic mutations in the family proband. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Whole Exome Sequencing | 10 months after recruiting | Whole Exome Sequencing will be performed in every subject from all families. All genetic variants will be filtered with bioinformatic tools. Genetic variants with putative biological effect, presents in affected CD patients and absents in their unaffected relatives will be further investigated (i.e. cosegregation with the disease, involvement in a given pathway....). This study remains a pilot study to identify genetic variants that may be involved in Crohn's Disease. |
Countries
France
Outcome results
None listed