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Inflammatory bowel diseases (IBD) and Parkinson disease (PD) are complex and multifactorial pathologies. Gut microbiota seems to play an active role. Indeed the digestive microbiota of patients with IBD or PD exhibits different compositions compared with asymptomatic subjects.
Bacterial translocation from gut to blood has been reported.
The investigators designed a case-control study to investigate the digestive microbiota and bacterial translocation during IBD and PD. The investigators want to evaluate gut microbiota bacteria involved in dysbiosis and bacterial translocation during IBD and PD. The investigators want to identify bacterial populations that can serve as biomarkers for clinical practice.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| IBD or PD patients | Experimental | 20 patients suffering from IBD 10 patients suffering from PD |
|
| Asymptomatic subjects | Active Comparator | 30 asymptomatic subjects matched to patients on age, sexe and BMI |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| stool and blood analysis | Other | High throughput sequencing and quantitative PCR |
|
| Measure | Description | Time Frame |
|---|---|---|
| 16S RNA sequencing in stool sample | 16S RNA sequencing to identify species constituting the microbiota in the stool | 2 years |
| 16S RNA sequencing in blood sample | 16S RNA sequencing to identify species constituting the microbiota in the blood | 2 years |
| Stool quantification of key bacteria associated with intestinal barrier permeability. | To determine stool rates of Faecalibacterium prausnitzii, Akkermansia muciniphila, Bacteroides fragilis, Clostridium difficile, Mycobacterium avium paratuberculosis and Escherischia coli by qPCR | 2 years |
| Blood quantification of key bacteria associated with intestinal barrier permeability. | To determine blood rates of Faecalibacterium prausnitzii, Akkermansia muciniphila, Bacteroides fragilis, Clostridium difficile, Mycobacterium avium paratuberculosis and Escherischia coli by qPCR | 2 years |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Philippe HALFON, MD, PhD | Hôpital Européen Marseille | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| European Hospital | Marseille | Bouches-du Rhone | 13003 | France |
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| ID | Term |
|---|---|
| D015212 | Inflammatory Bowel Diseases |
| D010300 | Parkinson Disease |
| ID | Term |
|---|---|
| D005759 | Gastroenteritis |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
| D007410 | Intestinal Diseases |
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| ID | Term |
|---|---|
| D003672 | Defecation |
| D006403 | Hematologic Tests |
| ID | Term |
|---|---|
| D004068 | Digestive System Physiological Phenomena |
| D055688 | Digestive System and Oral Physiological Phenomena |
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
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| D020734 | Parkinsonian Disorders |
| D001480 | Basal Ganglia Diseases |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D009069 | Movement Disorders |
| D000080874 | Synucleinopathies |
| D019636 | Neurodegenerative Diseases |
| D003933 | Diagnosis |
| D008919 | Investigative Techniques |