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Spondyloarthritis and inflammatory bowel diseases are common diseases, frequently met together in overlap syndromes. Their physiopathology remains puzzling. A strong role of gut microbiota has been recently put forward to explain the development of inflammatory bowel diseases, and is suspected to play an important role in rheumatoid diseases. Anti-Tumor Necrosis Factor (anti-TNF) alpha are effective and safe drugs in the treatment of both digestive and rheumatoid inflammatory diseases. The way they work is unclear, and the clinical response to this treatment is variable. A better understanding of the pathophysiology of inflammatory bowel diseases and of the action of anti-TNF alpha is essential to an optimized care.
Our hypothesis is that the efficacy of anti-TNF alpha in spondyloarthritis and in inflammatory bowel diseases is at least partly due to its restoring action of homeostasis at the interface between gastrointestinal mucosa and intestinal microbiota, either by primary action on the digestive epithelium, allowing it to regain its control and tolerance functions toward mucosal microbiota, either by direct action on the intestinal microbiota, via an inter-reigns regulation.
The main objective of our study is to assess quantitative and qualitative changes in fecal microbiota before (D0) and 3 months after initiation of anti-TNF alpha.
The investigators propose to conduct an exploratory study, on 10 spondyloarthritis and 20 inflammatory bowel diseases patients (10 Crohn's disease and 10 ulcerative colitis (UC), in which a first anti-TNF alpha treatment is indicated. At D0 and M3, intestinal microbiota will be studied by DNA16S sequencing and qPCR, via a stool sampling. Volatile Organic Compounds (VOCs) profile will be obtained by mass spectrometry. Blood lymphocytes profile will be obtained by flux cytometry. In addition, a colonoscopy will be performed at D0 for UC patients, with an endoscopic and histological assessment. A second short colonoscopy will be performed for UC patients at M3. At each time, clinical assessment will be performed.
A mirror group of 10 spondyloarthritis and 20 inflammatory bowel diseases patients (10 Crohn's disease and 10 ulcerative colitis), in which an "all but anti-TNF alpha or biotherapy" treatment is indicated will be included to distinguish the specific effects on microbiota of anti-TNF alpha.
12 patients by group will be included at M0 by anticipating that some patients will stop their treatment between M0 and M3, and consequently will be excluded from M3 sampling and from final analysis. Final analysis will be performed on 10 patients by group.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with anti-TNF alpha | Experimental | 12 spondyloarthritis and 24 inflammatory bowel diseases patients (12 Crohn's disease and 12 ulcerative colitis), in which a first anti-TNF alpha treatment is indicated. |
|
| mirror group | Active Comparator | A mirror group of 12 spondyloarthritis and 24 inflammatory bowel diseases patients (12 Crohn's disease and 12 ulcerative colitis), in which an "all but anti-TNF alpha or biotherapy" treatment is indicated will be included to distinguish the specific effects on microbiota of anti-TNF alpha. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| blood sample | Other | 14 ml whole blood for Peripheral blood mononuclear cell (PBMC) and monocytes isolation |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change from Baseline fecal microbiota profile by DNA 16S sequencing at 3 months | At 3 months from baseline |
| Measure | Description | Time Frame |
|---|---|---|
| Clinical response for Crohn Disease | Harvey-Bradshaw score | At baseline (day 0) and at 3 months from baseline |
| Clinical response for ulcerative colitis (UC) | Mayo score |
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Inclusion Criteria:
Patients aged over 18 years
Patients with the following conditions :
Patients naïve to anti-TNF alpha, justifying the initiation of an anti-TNF alpha treatment according to current guidelines (ECCO Inflammatory bowel disease (IBD) recommendations, the recommendations of the French Society of Rheumatology for SpA)
Patients agreeing to sign the informed consent
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Thomas BAZIN, MD | Assistance Publique - Hôpitaux de Paris | Study Director |
| Rodolphe THIEBAUT, Prof | University Hospital, Bordeaux | Study Chair |
| Pauline RIVIERE, MD | University Hospital, Bordeaux | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU de Bordeaux - service d'Hépato-gastroentérologie | Pessac | France |
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| stool samples | Other | Study of the fecal microbiota |
|
| food questionnaire | Other | food questionnaire on the seven days before the collection |
|
| colonoscopy | Other | Only for patients with ulcerative colitis (in routine care) |
|
| VOCs profile | Other | Volatile Organic Compounds (VOCs) profile obtained by mass spectrometry |
|
| At baseline (day 0) and at 3 months from baseline |
| Clinical response for spondyloarthritis (SpA) | BASDAI or Ankylosing Spondylarthritis Disease Activity Score (ASDAS) score | At baseline (day 0) and at 3 months from baseline |
| Ratio of circulating Th17 / Treg lymphocytes | At baseline (day 0) and at 3 months from baseline |
| Only for UC group : Analysis of endoscopic activity | Ulcerative Colitis Endoscopic Index of Severity (UCEIS) score | At baseline (day 0) and at 3 months from baseline |
| Only for UC group : Analysis of histological activity | Riley score | At baseline (day 0) and at 3 months from baseline |
| Change from Baseline Volatile Organic Compounds (VOCs) profile at 3 months | VOCs levels will be obtained from exhaled air samples analyzed by mass spectrometry | At baseline (day 0) and at 3 months from baseline |
| ID | Term |
|---|---|
| D025241 | Spondylarthritis |
| D003424 | Crohn Disease |
| D003093 | Colitis, Ulcerative |
| D015212 | Inflammatory Bowel Diseases |
| D007249 | Inflammation |
| ID | Term |
|---|---|
| D013166 | Spondylitis |
| D013122 | Spinal Diseases |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D005759 | Gastroenteritis |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
| D007410 | Intestinal Diseases |
| D003092 | Colitis |
| D003108 | Colonic Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D001800 | Blood Specimen Collection |
| D003113 | Colonoscopy |
| ID | Term |
|---|---|
| D013048 | Specimen Handling |
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
| D011677 | Punctures |
| D013514 | Surgical Procedures, Operative |
| D008919 | Investigative Techniques |
| D016099 | Endoscopy, Gastrointestinal |
| D016145 | Endoscopy, Digestive System |
| D003938 | Diagnostic Techniques, Digestive System |
| D004724 | Endoscopy |
| D003949 | Diagnostic Techniques, Surgical |
| D013505 | Digestive System Surgical Procedures |
| D019060 | Minimally Invasive Surgical Procedures |
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