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CompletedNCT02946710P75NTR-MNDUpdated Apr 3, 2018

P75NTR, Diagnostic Biomarker for Alzheimer's Disease: Quantification Study in Cerebrospinal Fluid

An observational study in Alzheimer Disease, sponsored by University Hospital, Toulouse. Completed at 1 site in France. Open to participants aged 40 Years and older. Per ClinicalTrials.gov, last updated 2018-04-03.

Sponsored by University Hospital, Toulouse · Observational

Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
120
Ages
40 Years and older
Sex
All
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Study summary

This research will be achieved by the assessment of p75NTR-ECD expression (total and linked to different species of Aβ (Aβ1-40 and Aβ-1-42)) within the cerebrospinal fluid (CSF) of patients with AD dementia, mild cognitive impairment (MCI) due to AD, frontotemporal dementia and non-neurodegenerative dementia.

Read the detailed description

Alzheimer's disease (AD) is a dementia which is clinically characterized by cognitive impairments with early memory loss and neuropathologically by two main lesions, amyloid deposits and tau protein accumulation. Presently, early diagnosis of AD relies on clinical symptoms, imaging techniques with recently introduced radio-tracers and analysis of cerebrospinal fluid biomarkers. All these tools are efficient when patients are already symptomatic and it is presently known that the lesions that might be reversible appear early in the time life of patients, several decades before the onset of clinical signs. To find a biomarker which would be detected early and tested in peripheral fluids is our challenge. According to updated physiopathology of the disease and referring to previous work on sphingolipid pathway in AD, precedent study focused attention on an original protein, p75NTR and particularly its extracellular domain (ECD). This protein is involved in the physiopathology of AD in several ways (apoptosis, survival). P75NTR-ECD interacts with Aβ, increases its solubility and accelerates its clearance.

The hypothesis of the present study is that p75NTR-ECD could be expressed differentially according to the category and stage of dementia. More precisely, this new biomarker could help for the diagnosis of AD and could also be used as an early marker of AD when tested in peripheral fluid.

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Conditions studied

  • Alzheimer Disease

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Keywords

  • Alzheimer disease
  • Alzheimer's disease, biomarkers
  • p75NTR-ECD
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In context

Alzheimer Disease

3,678 studies on the registry are indexed under Alzheimer Disease; 872 are open to participants now.

This study's enrollment of 120 is below the median of 200 across 751 observational studies indexed under Alzheimer Disease.

Browse Alzheimer Disease studies →

Lead sponsor

University Hospital, Toulouse is the lead sponsor of 794 studies on the registry; 214 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

CSF from patients with AD, patients with MCI due to AD, patients with frontotemporal dementia and patients with non-neurodegenerative dementia. Inclusion criteria according to Diagnostic and Statistical Manual-V (DSM-V) and updated NIA recommendations.

Inclusion criteria

  • patients with AD
  • patients with MCI due to AD,
  • patients with frontotemporal dementia
  • patients with non-neurodegenerative dementia, according to DSM-V and updated National Institute on Aging (NIA) recommendations

Exclusion criteria

Exclusion Criteria:

  • patients with Parkinson disease or Lewy body dementia
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Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
120 participants (actual)
Patient registry
No

Interventions

  • Biologicalcerebrospinal fluid

    Biological analysis on cerebrospinal fluid

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What researchers measure

Primary outcomes

  1. Concentration of p75NTR-ECD total

    Concentration of p75NTR-ECD total in CSF patients

    Time frame: Inclusion in the present study

Secondary outcomes

  1. Concentration of p75NTR-ECD bound to Aβ1-40 and Aβ1-42

    detection in CSF from patients

    Time frame: Inclusion in the present study

  2. expression of p75NTR-ECD between patient groups

    Differential expression of p75NTR-ECD between patient groups. Diagnostic and prognostic potential of p75NTR-ECD quantification.

    Time frame: inclusion in the present study

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Study locations

1 site
  • University Hospital of Toulouse
    Toulouse, France
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 3, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02946710
Lead sponsor
University Hospital, Toulouse
Responsible party
Sponsor
First posted
Oct 27, 2016
Start date
Dec 2014
Primary completion
Jun 2017
Completion
Dec 2017
Last update
Apr 3, 2018

Study contacts

Delisle Marie-Bernadette, MD
principal investigator · University Hospital, Toulouse

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.

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