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Longitudinal cerebrospinal fluid biomarker trajectories along the Alzheimer's disease continuum in the BIOMARKAPD study

  • Alberto Lleó
  • , Daniel Alcolea
  • , Pablo Martínez-Lage
  • , Philip Scheltens
  • , Lucilla Parnetti
  • , Judes Poirier
  • , Anja H Simonsen
  • , Marcel M Verbeek
  • , Pedro Rosa-Neto
  • , Rosalinde E R Slot
  • , Mikel Tainta
  • , Andrea Izaguirre
  • , Babette L R Reijs
  • , Lucia Farotti
  • , Magda Tsolaki
  • , Rik Vandenbergue
  • , Yvonne Freund-Levi
  • , Frans R J Verhey
  • , Jordi Clarimón
  • , Juan Fortea
  • Lutz Frolich, Isabel Santana, José Luis Molinuevo, Sylvain Lehmann, Pieter J Visser, Charlotte E Teunissen, Henrik Zetterberg, Kaj Blennow
109 Citationer (Scopus)

Abstract

Introduction: Within-person trajectories of cerebrospinal fluid (CSF) biomarkers in Alzheimer's disease (AD) are not well defined. Methods: We included 467 subjects from the BIOMARKAPD study with at least two serial CSF samples. Diagnoses were subjective cognitive decline (n = 75), mild cognitive impairment (n = 128), and AD dementia (n = 110), and a group of cognitively unimpaired subjects (n = 154) were also included. We measured baseline and follow-up CSF levels of total tau (t-tau), phosphorylated tau (p-tau), YKL-40, and neurofilament light (NfL). Median CSF sampling interval was 2.1 years. Results: CSF levels of t-tau, p-tau, NfL, and YKL-40 were 2% higher per each year of baseline age in controls (P <.001). In AD, t-tau levels were 1% lower (P <.001) and p-tau levels did not change per each year of baseline age. Longitudinally, only NfL (P <.001) and YKL-40 (P <.02) increased during the study period. Discussion: All four CSF biomarkers increase with age, but this effect deviates in AD for t-tau and p-tau.

OriginalsprogEngelsk
TidsskriftAlzheimer's & dementia : the journal of the Alzheimer's Association
Vol/bind15
Udgave nummer6
Sider (fra-til)742-753
Antal sider12
ISSN1552-5260
DOI
StatusUdgivet - jun. 2019

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