The Skin as a Window to the Central Nervous System in Frontotempolar Lombar Degeneration

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Frontotemporal lobar degeneration (FTLD) is a clinically heterogeneous syndrome, characterized by progressive decline in behaviour and/or language. From a pathological standpoint, like the great majority of neurodegenerative disorders, FTLD are proteinopathies, which are characterized by the presence of specific protein deposits in the Central Nervous System (CNS). Accordingly, the two main deposits observed in FTLD are either made of Tau or transactive response DNA binding protein 43 (TDP-43). In pathological conditions such as FTLD, both proteins are aggregated and hyperphosphorylated. It is now well established that the pathological process in some proteinopathies such as synucleinopathies (of which Parkinson's disease is the main representative) is not limited to the brain but also widespread throughout the peripheral autonomic networks, including the autonomic innervation of the skin. In this context, many independent studies have shown that the pathological process in PD could be detected using routine punch skin biopsies opening the way for the development of original histopathological markers of the disease. Our hypothesis is that such a scenario could also occur in FTLDs and that the detection of the pathological tau or TDP-43 protein in the skin could help in diagnosing FTLD. This is especially relevant as, despite the recent progress in genetics, neurobiology and neuroimaging, there are no available biomarkers for FTLD.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 75
Healthy Volunteers: t
View:

• Adressed or followed at memory clinic or ALS expert center at Nantes university hospital.

• Aged 50-75 years

• Fulfilling current diagnosis criteria for one of the disorder: vcfFTD, non-Alzheimer PPA (semantic or non fluent), DCB or PSP,ALS

• MMSE ≥ 18

• Membership of social security scheme

• No history of neurological disease, diabetes, or alteration/damage of peripheral nervous system

• Aged 50-75 years Paired to at least one patient on age (less or more 5 years)

• MOCA ≥ 26

• Membership of social security scheme

⁃ Non inclusion Criteria (Patients and healthy volunteers):

• Concomitting conditions affecting the peripheral nervous system such as but not limited to diabetes, renal failure, thyroid disorder, vitamin B12 deficiency, acute and chronic inflammatory diseases HIV, syphilis

• Know allergy to local anesthetic

• Known coagulopathy

• Pregnant women or breastfeeding women

• Person under court protection sous sauvegarde de justice

• Person under guardianship

• Inability to sign an informed consent

⁃ Non inclusion criteria (Patients) • Patient with neurological disease other than FTLD

⁃ Non inclusion criteria (Healthy volunteers) :

⁃ • Evidence of neurological disorder at the inclusion including but not limted to FTLD, Parkinson disease, Alzheimer disease, lewy body dementia, Huntington disease, systemic lupus erythematosus multiple sclerosis; learning disabilities, mental retardation, severe hypoxic brain injuries, brain trauma with permanent cognitive impairments.

Locations
Other Locations
France
Nantes University Hospital
RECRUITING
Nantes
Contact Information
Primary
Claire BOUTOLEAU-BRETONNIERE, MD
claire.boutoleaubretonnière@chu-nantes.fr
02 40 16 54 22
Backup
pascal DERKINDEREN, Pr
derkinderenp@yahoo.fr
02 40 16 54 22
Time Frame
Start Date: 2024-12-17
Estimated Completion Date: 2027-07
Participants
Target number of participants: 80
Treatments
Other: Single arm study
A single 3 mm-diameter punch skin biopsy will be obtained from FTLD patients and healthy volunteers at the C8 paravertebral under local anesthesia to analyze cutaneous innervation
Sponsors
Leads: Nantes University Hospital

This content was sourced from clinicaltrials.gov