RECRUITINGOBSERVATIONAL
Alteration of Symbiosis Intestinal Microbiota on Patients With Anorexia Nervosa
Study of Translational Process of Relationship Between Intestinal Microbiota of Dysbiosis and the Psychic Symptoms of Anorexia Nervosa (Eating Disorders and Anxio-depression Disorders)
About This Trial
The purpose of this study will be to study the association between the level of psychic symptomatic of anorexia nervosa (AN) (intensity of food restriction, symptoms of anxiety and depression) and alteration of host environment symbiosis and the mechanism (dysbiosis of intestinal microbiota, increase of intestinal permeability, immunity alteration and low-grade inflammation).
Who May Be Eligible (Plain English)
Who May Qualify:
For patients:
- Patients aged ≥18 years;
- Anorexia according to DSM-5 and CIDI (Composite International Diagnostic Interview);
- Body mass index (BMI) (P/T2) \< 15;
- Hospitalization for nutrition rehabilitation;
- Covered by a health insurance;
- willing to sign a consent form form signed.
For Healthy Volunteers:
- Aged ≥18 years;
- 18.5 \< BMI (P/T2) \< 25;
- Covered by a health insurance;
- willing to sign a consent form form signed.
Who Should NOT Join This Trial:
For patients:
- Patients no-responding all criteria of DSM-5 or CIDI scores;
- Taken of antibiotic treatment 2 months / or laxativ 3 weeks before hospitalization;
- Somatic comorbidity should perturb intestinal microbiota (Crohn's disease, diabetes and all other chronic inflammatory diseases);
- Patients under guardianship;
- Patients covered by french AME scheme.
For Healthy Volunteers:
- Any disease should perturb intestinal microbiota;
- Recent ponderal variation;
- Taken of antibiotic treatment 2 months or laxativ 3 weeks before hospitalization;
- Under guardianship;
- Covered by french AME scheme.
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
For patients:
* Patients aged ≥18 years;
* Anorexia according to DSM-5 and CIDI (Composite International Diagnostic Interview);
* Body mass index (BMI) (P/T2) \< 15;
* Hospitalization for nutrition rehabilitation;
* Covered by a health insurance;
* Informed consent form signed.
For Healthy Volunteers:
* Aged ≥18 years;
* 18.5 \< BMI (P/T2) \< 25;
* Covered by a health insurance;
* Informed consent form signed.
Exclusion Criteria:
For patients:
* Patients no-responding all criteria of DSM-5 or CIDI scores;
* Taken of antibiotic treatment 2 months / or laxativ 3 weeks before hospitalization;
* Somatic comorbidity should perturb intestinal microbiota (Crohn's disease, diabetes and all other chronic inflammatory diseases);
* Patients under guardianship;
* Patients covered by french AME scheme.
For Healthy Volunteers:
* Any disease should perturb intestinal microbiota;
* Recent ponderal variation;
* Taken of antibiotic treatment 2 months or laxativ 3 weeks before hospitalization;
* Under guardianship;
* Covered by french AME scheme.
Treatments Being Tested
BIOLOGICAL
Stool and blood samples
Stool and blood samples
Locations (1)
Service de Nutrition Clinique, Hôpital Paul Brousse (APHP)
Villejuif, France