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The goal of this longitudinal study is to (1) explore the association between the gut microbiota and inflammatory disease activity in early onset multiple sclerosis, (2) investigate whether/how gut microbial composition vary when patients experience a relapse, and (3) to assess whether the gut microbiota shows increased similarities between affected pairs of first-degree relatives within the same family when compared with discordant pairs of first-degree relatives.
Using metagenomics, as well as clinical, immunological, and radiological observations, the investigators will investigate if active relapsing-remitting multiple sclerosis patients have a more pro-inflammatory gut microbiota signature than multiple sclerosis patients with less active disease and matched healthy controls.
More specifically, the investigators will investigate whether temporal variability of the gut microbiota is related to inflammatory disease activity in multiple sclerosis, whether changes in the gut microbiota are predictive of future inflammatory disease activity in multiple sclerosis, and whether gut microbiota characteristics are predictive of the disease course after 2 years.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Multiple sclerosis (MS) patients | Experimental | Patients will undergo magnetic resonance imaging (MRI). Stool and blood samples will be collected. |
|
| Healthy controls | No Intervention | Healthy controls will not undergo magnetic resonance imaging (MRI). Stool and blood samples will be collected. | |
| Multiple sclerosis (MS) patients undergoing a relapse | No Intervention | Multiple sclerosis (MS) patients undergoing a relapse will not undergo magnetic resonance imaging (MRI). Stool and blood samples will be collected. | |
| Multiple sclerosis (MS) patients from multiplex MS families | No Intervention | Multiple sclerosis (MS) patients from multiplex MS families will not undergo magnetic resonance imaging (MRI). Stool and blood samples will be collected. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Magnetic resonance imaging (MRI) | Other | MRI scanner |
|
| Measure | Description | Time Frame |
|---|---|---|
| Clinical evidence for active disease | Time to first relapse (after baseline) will be reported for all patients. | 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| Radiological evidence for active disease | Occurrence of new contrast-enhancing T1 hyper intense lesions, or changes in white matter lesion volume (i.e. new or enlarging T2 hyper intense lesions) | 3 years |
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Inclusion Criteria patients:
Exclusion Criteria patients:
Additional inclusion criteria for MS patients undergoing a relapse:
• Ability to provide a faecal sample within 4 weeks from onset of the first symptoms suggestive of a relapse, before cortisone treatment. A relapse is defined by a new clinical sign or clinical worsening of a previous sign/symptom persisting for >=24 hours in the absence of fever.
Additional exclusion criteria for MS patients undergoing a relapse:
Inclusion criteria healthy controls:
Exclusion criteria healthy controls:
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| Name | Affiliation | Role |
|---|---|---|
| Marie D'hooghe, M.D. | National MS Center Melsbroek | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Universitair Ziekenhuis Brussel | Jette | Brussels Capital | 1090 | Belgium | ||
| Nationaal Multiple Sclerose Centrum Melsbroek |
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| ID | Term |
|---|---|
| D009103 | Multiple Sclerosis |
| ID | Term |
|---|---|
| D020278 | Demyelinating Autoimmune Diseases, CNS |
| D020274 | Autoimmune Diseases of the Nervous System |
| D009422 | Nervous System Diseases |
| D003711 | Demyelinating Diseases |
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| ID | Term |
|---|---|
| D009682 | Magnetic Resonance Spectroscopy |
| ID | Term |
|---|---|
| D013057 | Spectrum Analysis |
| D002623 | Chemistry Techniques, Analytical |
| D008919 | Investigative Techniques |
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| Melsbroek |
| Vlaams-Brabant |
| 1820 |
| Belgium |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |