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Amyloid Beta-peptide 1-40 and Alzheimer's Disease

Not Applicable
Completed
Conditions
Alzheimer Disease
Interventions
Biological: spinal fluid collection
Registration Number
NCT02770482
Lead Sponsor
CHU de Reims
Brief Summary

The combined measurement of Ab42 and tau protein (total and phosphorylated) in the spinal fluid has been shown to be promising in the diagnosis of Alzheimer's disease (AD), and has justified its inclusion new diagnostic criteria. However, it can sometimes yield discordant results that are not discriminant (isolated variation in Ab42 or P-181 Tau). To answer this challenge, a new marker has been developed in recent years, namely amyloid beta-peptide 1-40 (Aβ40). This marker reflects the patient's total amyloid deposits and is used to calculate the Aβ42/Aβ40 ratio. This ratio measures the relative variation of Aβ42 as compared to the total amyloid burden. Literature data on this topic are sparse and to date, no report has been published evaluating the utility of this marker in the diagnostic strategy for AD.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
204
Inclusion Criteria
  • Patients attending the Memory Clinic of Champagne-Ardennes for memory disorders, and
  • Whose diagnostic work-up requires assessment of biomarkers present in the cerebrospinal fluid are considered eligible for inclusion in this study.
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Exclusion Criteria
  • Patients who do not have any social security coverage will not be included.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
AD Patientsspinal fluid collection-
Primary Outcome Measures
NameTimeMethod
Percentage of diagnostic certitude for AD (diagnosed cases)six months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Chu de Reims

🇫🇷

Reims, France

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