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Recruiting Observational

Tanycytes in Alzheimer's Disease and Frontotemporal Dementia

NCT05288842 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2022-09-06
Last updated
2026-05-18

Condition(s) studied

Alzheimer DiseaseFrontotemporal Dementia

Investigational drug(s) / intervention(s)

Lumbar puncture →blood sample →

Lumbar puncture: 5 mL of CSF

blood sample: 6x5 mL of blood sample collected :1 dry tube, 2 EDTA tubes, 1 fluoride tube, and 2 polypropylene tubes

Study summary

Metabolic and hormonal deregulations are both a risk factor and a hallmark of Alzheimer's disease (AD) and frontotemporal dementia (FTD), occurring early in the course of the disease. In FTD in particular, hyperorality and dietary changes are associated with metabolic and hormonal changes such as altered levels of the anorexigenic hormone leptin.

The hypothalamus is a brain region that controls metabolism and hormonal systems. Hypothalamic function depends on its ability to sense peripheral signals. The hypothalamus sits on a circumventricular organ called the median eminence (ME) that puts it in contact with systemic blood circulation. In the ME, fenestrated capillaries allow the diffusion of bloodborne factors. However, despite the lack of blood-brain barrier at brain microvessels, diffusion is controlled by specialized ependymoglial cells, the tanycytes, which exert a barrier function between the ME and the third ventricle and controls the access of blood-borne molecules into the hypothalamus. Previous work from our laboratory and the ERC consortium has highlighted the role of tanycytes not only in the regulation of the release of neurohormones from neuroendocrine nerve terminals into the pituitary portal blood circulation, but also in the transport of circulating leptin into the hypothalamus. Hence hypothalamic dysfunction in AD and FTD can result either from dysregulation of neuroendocrine secretions, direct neuronal loss or from defective transport (and hence resistance) to hormones like leptin.

This study is to demonstrate that leptin transport though tanycytes is early altered in FTD and AD and correlates

Eligibility

Sex
ALL
Min age
40 Years
Max age
85 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Subjects able to undergo a lumbar puncture * Subjects registered with the French Social Security, in agreement with the French law on biomedical experimentation To be assigned in the study subgroups, subjects will have to fulfill the specific following criteria: Group 1: Controls * absence of cognitive complaint (completion of the memory complaint questionnaire) * absence of significant cognitive impairment: normal MMSE according to age and education levels * Subjects capable of and willing to comply with the protocol and to give their written informed consents after having received and understood the subject information Group 2: Alzheimer's Disease * Diagnosis of probable Alzheimer's disease dementia according to the NIA 2011 criteria1 * MMSE ≥ 16 * Subjects who have a study partner. The study partner is required to complete several scales and to drive back the subject after the lumbar puncture for safety reasons. If the subjects or their study partners are not able to drive, their transport fees will be reimbursed by the promotor * Subjects and study partners capable of and willing to comply with the protocol and to give their written informed consents after having received and understood the subject information. According to the legal protection or the mental capacities of the subject, the subject will be accompanied by a legally acceptable representative during this procedure Group 3: Frontotemporal Dementia * Diagnosis of probable frontotemporal dementia according to the FTDC 2011 criteria2 * MMSE ≥ 16 * Subjects who have a study partner. The study partner is required to complete several scales and to drive back the subject after the lumbar puncture for safety reasons. If the subjects or their study partners are not able to drive, their transport fees will be reimbursed by the promotor * Subjects and study partners capable of and willing to comply with the protocol and to give their written informed consents after having received and understood the subject information. According to the legal protection or the mental capacities of the subject, the subject be accompanied by a legally acceptable representative during this procedure Exclusion Criteria: * General exclusion criteria: * Subjects with dementia caused by a non-neurodegenerative disease, including patients with severe cerebrovascular risk factor load * Subjects who have contraindications to perform a lumbar puncture * Subjects who have contraindications to perform a MRI scan * Weighted less than 45 kg Associated illnesses or conditions: * Subjects with other neurodegenerative disease such as Lewy body dementia and Parkinson's disease * Subjects with other serious neurological disorder such as brain tumor, stroke, epilepsy, hydrocephalus and any condition which contraindicates, in the investigator's judgment, entry to the study; * Subjects with severe metabolic or endocrine disorder (excluding hypothyroidism under stable hormone replacement therapy, controlled type 2 diabetes or common dyslipidaemia), previously known or identified at screening * Subjects under metformin treatment. Biological exclusion criteria: * Subjects with known active HCV, HBV or HIV * Subjects with clinical or significant laboratory abnormalities, previously known or identified at screening, in the judgment of the investigator Others: * Pregnancy or breastfeeding or Women of childbearing age without effective contraception (a pregnancy test will be done) * Subjects with excessive alcohol intake or drug abuse, in the judgment of the investigator * Subjects who, in the opinion of the investigator, have a risk of non-compliance to the study procedures or who are otherwise not appropriate to include in this clinical trial (for example, being impossible to contact in case of emergency)

Primary outcome measure(s)

  • Mean CSF-to-blood ratio (CBR) of leptin concentration. — At visit 2, occurring 1 to 90 days after visit 1(Baseline)
    Leptin concentration in blood and CSF (in the pg/mL range) will be measured by enzyme-linked immunosorbent assay (ELISA).

Trial sites (1)

FacilityCityRegionStatus
Memory Resources and Research Center Lille Lille France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05288842 on ClinicalTrials.gov ↗ ← All trials in France