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General inclusion criteria:
- age ≥ 18 years-old
- national health insurance cover
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Patients inclusion criteria:
- genetically confirmed Huntington’s disease diagnosis (≥ 35 CAG repeat in HTT gene exon 1)
- written informed consent
- only for patients “with lumbar puncture (LP)”: patient agreement for LP
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Control inclusion criteria:
- anterior LP for medical reason with consent for biobank “Neuro” with following samples present in this biobank : 2 mL blood + 0.5 mL plasma + 0.5 mL cerebrospinal fluid
- information and non-opposition for the finality of this biobank
- paired by age with a patient (+/- 5 years difference)
About
The main purpose of this study is to be able to confirm whether a protein called BDNF is a biomarker for the expression of HD in humans. The study will recruit 135 participants who will be followed for a period of 2 years. Their levels of BDNF will be measured in samples taken both from the cerebrospinal fluid (CNF) and blood. The symptom development in the 2 year trial period, will also be monitored with brain imaging and by testing cognitive functions. The study will investigate how the levels of BDNF in the blood and the CSF differ or correspond. The study will also try to identify the connection between BDNF levels and symptom development. Why is this study important? We have good reasons to believe that BDNF has an active role in protecting damaged brain cells as well as enhancing growth of new ones. The study will provide us with more solid information about the connection between BDNF and symptom development in humans with HD. If proven to be relevant, BDNF levels will probably be a target for treatment in the future. In this study the BDNF levels in CSF and blood will hopefully be identified as a biomarker for HD. We need biomarkers to measure if a treatment has positive effect or not.
Sponsored by
University Hospital, Montpellier
Countries
France
Number of participants
20 participants
Recruitment status
Not yet Recruiting
Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
Sexes Eligible for Study: All
Accepts Healthy Volunteers: Yes
Inclusion Criteria
Exclusion Criteria
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General exclusion criteria:
- protected by law
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Patients exclusion criteria:
- Huntington’s disease stage too Evolved that may interfere with cognitive evaluations or MRI
- contraindications to brain MRI
- only for patients “with LP”: contraindications to LP
- incapacity to give informed consent
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Control exclusion criteria:
- neurodegenerative of inflammatory central nervous system pathology
FRANCE
Trial site: University Hospital of Montpellier |
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Status: [maxbutton id=”2″ ] |
Address: Montpellier, France |
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Contact: Cecilia Marelli Contact: Diana Ban
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Telephone: Not available at the moment Telephone: Not available at the moment
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Email: c-marelli@chu-montpellier.fr Email: d-ban@chu-montpellier.fr
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