Neuroinflammation in Amyotrophic Lateral Sclerosis - Mechanisms and Therapeutic Perspectives: a Translational Pilot Study Among ALS Patients
- Conditions
- Amyotrophic Lateral Sclerosis (ALS)
- Interventions
- Other: Blood sampleOther: ALS Functional rating Scale-revised (ALS FRS-R)Other: slow vital capacityOther: Cerebrospinal Fluid (CSF) sample
- Registration Number
- NCT02424669
- Lead Sponsor
- Assistance Publique Hopitaux De Marseille
- Brief Summary
Amyotrophic Lateral Sclerosis (ALS) is the most common motor neuron diseases. It is considered as a rare disease with a prevalence of about 8 per 100,000 persons. Initiating in mid-life by progressive paralysis, it evolves rapidly into a generalized muscle wasting that leads irrevocably to death within 2 or 5 years of clinical onset.
Since there is no cure for ALS, the management of the disease is supportive and palliative. Riluzole is the only drug that has been shown to extend survival by about three months. The identification of biomarkers sensitive to the progression of the disease might enhance the diagnostic and provide new drug targets.
Dysfunction of the immune system is a pathological hallmark of ALS. Increased levels of interferon gamma (IFNgamma) were found in the serum and cerebrospinal fluid (CSF) of ALS patients. However, the cell origin as well as the pathogenic influence of this peripheral source of IFNg is unknown. Thus, IFNgamma might have a role in the pathogenic process of ALS and might be a potential biomarker of the disease.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 100
Group 1 and Group 2:
- with sporadic ALS (without family history), recently diagnosed (onset of first symptoms < 24 months) group 1, not recently diagnosed (onset of first symptoms > 24 months) group 2
- Who meet the laboratory-supported probable, probable or definite form of ALS according to the El Escorial criteria
- Suffering from the spinal form of ALS
Group 3:
- with an inflammatory peripheral neuropathy, or a non inflammatory peripheral neuropathy, recently diagnosed
- Familial form of ALS
- Bulbar form and respiratory onset form of ALS
- Subjects with a clinically significant history of unstable or severe cardiac, oncologic, hepatic or renal disease, or other medically significant illness.
- Subjects with significant cognitive impairment, clinical dementia, or psychiatric illness.
- Female of childbearing potential (apart of patient using adequate contraceptive measures), pregnant or breast feeding
- Suspected inability to complete the study follow-up (foreign workers, transient visitors, tourists or any others for whom follow-up evaluation is not assured)
- Participation in any other clinical study within 30 days prior to the Screening Visit
- Persons deprived of freedom by judicial or administrative decision, hospitalized without their consent or for other reasons than the research, under legal protection or unable to express their consent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description not recently diagnosed ALS patients slow vital capacity - not recently diagnosed ALS patients Cerebrospinal Fluid (CSF) sample - patients with peripheral neuropathy, recently diagnosed Blood sample - not recently diagnosed ALS patients Blood sample - recently diagnosed ALS patients ALS Functional rating Scale-revised (ALS FRS-R) - recently diagnosed ALS patients slow vital capacity - not recently diagnosed ALS patients ALS Functional rating Scale-revised (ALS FRS-R) - recently diagnosed ALS patients Blood sample - recently diagnosed ALS patients Cerebrospinal Fluid (CSF) sample -
- Primary Outcome Measures
Name Time Method ALS Functional rating Scale-revised (ALS FRS-R) score 12 months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Assistance Publique Hôpitaux de Marseille
🇫🇷Marseille, France