Identification of Retinal Perivascular Inflammation in Patients With Multiple Sclerosis Using Adaptive Optics (RETIMUS)
Study Details
Study Description
Brief Summary
Using a technique called adaptive optics imaging applied on retina, investigators aim to gain access to vascular changes that could occur early in the course of Multiple Sclerosis (MS) and which could reflect vascular changes occurring along the optic nerve of the brain parenchyma. Indeed, our team has been able to develop a quantitative method to measure the perivascular infiltrate in the retina of patients with various inflammatory retinal disease. It has been observed in MS patients that this perivascular infiltrate can also be detected in the retina. However, its distribution across MS phenotypes (relapsing or progressive MS, with and without optic neuritis) is still unknown.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
This is a monocentric pathophysiological, interventional, prospective, open label, non-randomized pilot study which aims to identify in patients with MS at different stages if the presence of retinal perivascular inflammation can be detected and quantified using adaptive optics, which is a non-invasive examination.
Investigators will recruit MS patients in 3 subgroups, depending on their phenotype (Relapsing Remitting Multiple Sclerosis (RRMS) without optic neuritis, RRMS with optic neuritis, progressive MS), with 15 patients in each group.
15 healthy volunteers (HV) will also be enrolled.
The comparison of these groups is necessary to determine if there are significant differences, allowing us to highlight biomarkers in MS patients in order to enable highly efficient and robust trials designs in the future.
To test the hypothesis, the study has 3 visits over 6 months (M0, M3 and M6). Neurological evaluation, blood sample, imaging, ophthalmologic evaluation and Adaptive optics ophthalmoscopy assessments will be performed.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: MS patients RRMS Patients with optic neuritis, RRMS patients without optic neuritis or Progressive MS patients |
Other: Adaptive Optics Ophthalmoscopy (AOO)
AOO will permit to detect and quantify retinal perivascular inflammation in patients with MS in comparison to Healthy volunteers (control group)
|
| Other: Control group Healthy volunteers |
Other: Adaptive Optics Ophthalmoscopy (AOO)
AOO will permit to detect and quantify retinal perivascular inflammation in patients with MS in comparison to Healthy volunteers (control group)
|
Outcome Measures
Primary Outcome Measures
- Quantification of retinal perivascular cuff width across MS phenotypes [Baseline]
The primary endpoint is to quantify retinal perivascular cuff width across MS phenotypes, compared among a group of control at baseline.
Secondary Outcome Measures
- Variation of size of perivascular sheathing [month 3 and month 6]
Variation of size of perivascular sheathing along retinal vessels in the posterior pole during follow up (at month 3 and month 6) in patients with MS and a group of control
- Clinical disability measure with EDSS [month 3 and month 6]
Evolution of Clinical disability: Expanded Disability Status Scale (EDSS: 0: normal neurological exam; 10 : death of the patient) at month 3 for MS patients with optic neuritis and at month 6 for all MS patients
- Clinical disability measured with MSFC [month 3 and month 6]
Evolution of Clinical disability: Multiple Sclerosis Functional Composite (MSFC) at month 3 for MS patients with optic neuritis and at month 6 for all MS patients
- Number of relapses [month 3 and month 6]
Evolution of Clinical disability: number of relapses at month 3 for MS patients with optic neuritis and at month 6 for all MS patients
- Presence of disc oedema measured at Optical Coherence Tomography (OCT) measurements [month 3 and month 6]
Evolution of OCT measurements (presence of disc oedema) at month 3 for MS patients with optic neuritis and at month 6 for all MS patients
- RNLF thickness measured at Optical Coherence Tomography (OCT) measurements [month 3 and month 6]
Evolution of OCT measurements : retinal nerve fiber layer thickness (RNFL, µm) at month 3 for MS patients with optic neuritis and at month 6 for all MS patients
- parenchymal T2 lesion volume at MRI [Baseline]
Evolution of MRI metrics: parenchymal T2 lesion volume
- gadolinium enhanced T1 lesion at MRI [Baseline]
Evolution of MRI metrics: gadolinium enhanced T1 lesion
- optic nerve cross-sectional area at MRI [Baseline]
Evolution of MRI metrics: optic nerve cross-sectional area
- Hyperintensity on the optic nerve at MRI [Baseline]
Evolution of MRI metrics: Hyperintensity on the optic nerve
Eligibility Criteria
Criteria
Inclusion Criteria:
Group 1:
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Age between 18 and 60 years old.
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Relapsing remitting MS (criteria of McDonald 2017)
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Less than 10 years of disease duration
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Subject who has never presented a clinical episode of optic neuritis
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Affiliation to a social security scheme or beneficiary of such a scheme
Group 2:
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Age between 18 and 60 years old
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Relapsing remitting MS (criteria of McDonald 2017)
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Less than 10 years of disease duration
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Subject presenting an acute episode of retrobulbar optic neuritis within 3 months from onset
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After optimal treatment for the retrobulbar optic neuritis
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Affiliation to a social security scheme or beneficiary of such a scheme
Group 3:
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Age between 18 and 60 years old
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Primary or Secondary progressive multiple sclerosis within 10 years of progressive phase;
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Affiliation to a social security scheme or beneficiary of such a scheme
Group 4 (Healthy Subjects):
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Age between 18 and 60 years old
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Affiliation to a social security scheme or beneficiary of such a scheme
Exclusion Criteria:
For all patients (Group 1; 2; 3):
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Corticosteroid treatment within one month from inclusion
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Other neurological, ophthalmologic or systemic disease;
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Severe symptoms of uncontrolled chronic disease (renal, hepatic, hematologic, gastro-intestinal, pulmonary or cardiac or any intercurrent uncontrolled disease at inclusion)
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Severe renal dysfunction (glomerular filtration rate < 30mL/min). This non-inclusion criteria will be verified by serum creatinine test within six months from inclusion;
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Contraindication for MRI;
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Pregnancy or breast-feeding;
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Unwillingness to be informed in case of abnormal MRI (with a significant medical anomaly)
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Incapacity to understand or sign the consent form;
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Adults legally protected (under judicial protection, guardianship, or supervision), persons deprived of their liberty.
For healthy subjects (Group 4):
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Neurological, ophthalmologic or systemic disease;
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Severe symptoms of uncontrolled chronic disease (renal, hepatic, hematologic, gastro-intestinal, pulmonary or cardiac or any intercurrent uncontrolled disease at inclusion);
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Contraindication for MRI;
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Pregnancy or breast-feeding;
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Unwillingness to be informed in case of abnormal MRI (with a significant medical anomaly)
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Incapacity to understand or sign the consent form;
-
Adults legally protected (under judicial protection, guardianship, or supervision), persons deprived of their liberty.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Institut du Cerveau et de la Moelle epiniere - Hopital Pitie Salpetriere | Paris | France |
Sponsors and Collaborators
- Institut National de la Santé Et de la Recherche Médicale, France
- Biogen
Investigators
- Principal Investigator: Celine Louapre, MD, PHD, Institut du Cerveau et de la Moelle Epinière
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 19-25