Crohn Disease
Conditions
Brief summary
This research study will evaluate if specific blood, stool and MRI tests can tell the difference between bowel wall inflammation without scarring and bowel wall inflammation with scarring that can cause bowel blockages requiring surgery.
Detailed description
This multi-center study will test the accuracy of individual and combined MRI and blood-based diagnostic tools in both children and adults with small bowel CD. We will determine the accuracy of a composite tool (including its multiple individual biomarkers) for defining the relative amounts of intestinal inflammation versus scarring in patients at the time of surgery (B2 disease) and in patients at an early stage of disease prior to complications (B1 disease).
Interventions
biomarkers to distinguish fibrotic vs non-fibrotic CD lesions
fecal biomarkers of inflammation, mucosal inflammation
MRI imaging to detect bowel wall fibrosis and to detect inflamed, non-fibrotic from inflamed, fibrotic bowel
Sponsors
Study design
Eligibility
Inclusion criteria
* Aim 1 (CD participants) 1. Aged 8-70 years 2. Undergoing first surgical distal (ileal) small bowel resection for structuring (B2 phenotype) Crohn's disease as determined by CTE or MRE or ileocolonoscopy 3. English speaking * Aim 2 (CD participants) 1. Age 8 to 70 years 2. Uncomplicated inflammatory small bowel CD based on clinical CTE or MRE or ileocolonoscopy performed within 6 months prior to enrollment (CD participants only) 3. English speaking * Aim 2 (Control participants) 1. Age 8 to 70 years 2. English speaking
Exclusion criteria
* Aim1 (CD participants) 1. B1 or B3 (i.e., fistula, abscess, phlegmon/inflammatory mass) CD phenotype 2. Prior small bowel surgery, including but not limited to surgical resection, stricturoplasty, or endoscopic treatment of a small bowel stricture 3. Anything to eat or drink within 4 hours of study visit (participants may take their required medications with a little water) 4. Known pregnancy (Note: Institutional policies/procedures will be followed for pregnancy screening) 5. Contraindication for MRI (e.g., surgical implant, claustrophobia). Note: To be determined based on local procedures. * Aim 2 (CD participants) 1. Stenotic ileocecal valve at colonoscopy 2. Prior small bowel surgery, including but not limited to surgical resection, stricturoplasty, or endoscopic treatment of a small bowel stricture 3. Anything to eat or drink within 4 hours of study visit (participants may take their required medications with a little water) 4. Known pregnancy (Note: Institutional policies/procedures will be followed for pregnancy screening) 5. Contraindication for MRI (e.g., surgical implant, claustrophobia). Note: To be determined based on local procedures. * Aim 2 (Control participants) 1. Any known gastrointestinal tract disease 2. Any known inflammatory/autoimmune disease involving another organ system (e.g., rheumatoid arthritis, scleroderma, multiple sclerosis). 3. Fecal calprotectin level of ˃100 mcg.gm will be excluded from further analysis and replaced.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Magnetization transfer ratio (MTR) | Day 1 | compare MTR values between Aim 1 and Aim 2 cohorts |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Correlation between MTR values and bowel wall collagen measurements | Day 1 | combine all subjects from Aim 1 and Aim 2 that undergo MRI |
Countries
United States