The Cerebrospinal Fluid Aβ1–42/Aβ1–40 Ratio Improves Concordance with Amyloid-PET for Diagnosing Alzheimer’s Disease in a Clinical Setting

نویسندگان

  • Ellis Niemantsverdriet
  • Julie Ottoy
  • Charisse Somers
  • Ellen De Roeck
  • Hanne Struyfs
  • Femke Soetewey
  • Jeroen Verhaeghe
  • Tobi Van den Bossche
  • Sara Van Mossevelde
  • Johan Goeman
  • Peter Paul De Deyn
  • Peter Mariën
  • Jan Versijpt
  • Kristel Sleegers
  • Christine Van Broeckhoven
  • Leonie Wyffels
  • Adrien Albert
  • Sarah Ceyssens
  • Sigrid Stroobants
  • Steven Staelens
  • Maria Bjerke
  • Sebastiaan Engelborghs
چکیده

BACKGROUND Evidence suggests that the concordance between amyloid-PET and cerebrospinal fluid (CSF) amyloid-β (Aβ) increases when the CSF Aβ1-42/Aβ1-40 ratio is used as compared to CSF Aβ1-42 levels alone. OBJECTIVE In order to test this hypothesis, we set up a prospective longitudinal study comparing the concordance between different amyloid biomarkers for Alzheimer's disease (AD) in a clinical setting. METHODS Seventy-eight subjects (AD dementia (n = 17), mild cognitive impairment (MCI, n = 48), and cognitively healthy controls (n = 13)) underwent a [18F]Florbetapir ([18F]AV45) PET scan, [18F]FDG PET scan, MRI scan, and an extensive neuropsychological examination. In a large subset (n = 67), a lumbar puncture was performed and AD biomarkers were analyzed (Aβ1-42, Aβ1-40, T-tau, P-tau181). RESULTS We detected an increased concordance in the visual and quantitative (standardized uptake value ratio (SUVR) and total volume of distribution (VT)) [18F]AV45 PET measures when the CSF Aβ1-42/Aβ1-40 was applied compared to Aβ1-42 alone. CSF biomarkers were stronger associated to [18F]AV45 PET for SUVR values when considering the total brain white matter as reference region instead of cerebellar grey matterConclusions:The concordance between CSF Aβ and [18F]AV45 PET increases when the CSF Aβ1-42/Aβ1-40 ratio is applied. This finding is of most importance for the biomarker-based diagnosis of AD as well as for selection of subjects for clinical trials with potential disease-modifying therapies for AD.

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عنوان ژورنال:

دوره 60  شماره 

صفحات  -

تاریخ انتشار 2017