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Improved Cerebrospinal Fluid-Based Discrimination between Alzheimer's Disease Patients and Controls after Correction for Ventricular Volumes

  • Linda J.C. Van Waalwijk Van Doorn
  • , Juan D. Gispert
  • , H. Bea Kuiperij
  • , Jurgen A.H.R. Claassen
  • , Andrea Arighi
  • , Inês Baldeiras
  • , Kaj Blennow
  • , Marco Bozzali
  • , Miguel Castelo-Branco
  • , Enrica Cavedo
  • , Derya D. Emek-Savaş
  • , Erden Eren
  • , Paolo Eusebi
  • , Lucia Farotti
  • , Chiara Fenoglio
  • , Juan Fortea Ormaechea
  • , Yvonne Freund-Levi
  • , Giovanni B. Frisoni
  • , Daniela Galimberti
  • , Sermin Genc
  • Viviana Greco, Harald Hampel, Sanna Kaisa Herukka, Yawu Liu, Albert Lladó, Alberto Lleó, Flavio M. Nobili, Kader K. Oguz, Lucilla Parnetti, João Pereira, Agnese Picco, Maria Pikkarainen, Catarina Resende De Oliveira, Esen Saka, Nicola Salvadori, Raquel Sanchez-Valle, Isabel Santana, Elio Scarpini, Philip Scheltens, Hilkka Soininen, Roberto Tarducci, Charlotte Teunissen, Magda Tsolaki, Andrea Urbani, Eduard Vilaplana, Pieter Jelle Visser, Asa K. Wallin, Görsev Yener, José L. Molinuevo, Olga Meulenbroek, Marcel M. Verbeek*
*Corresponding author for this work
  • Radboud University Medical Center
  • Pasqual Maragall Foundation
  • CIBER - Center for Biomedical Research Network
  • Pompeu Fabra University
  • University of Milan
  • Centro Hospitalar e Universitário de Coimbra
  • University of Gothenburg
  • Sahlgrenska University Hospital
  • IRCCS Fondazione Santa Lucia - Roma
  • University of Coimbra
  • Universite Paris Sorbonne - Paris IV
  • Dokuz Eylul University
  • University of Perugia
  • Institut de Recerca de LHospital de la Santa Creu i Sant Pau
  • Karolinska Institutet
  • Karolinska University Hospital
  • IRCCS Centro San Giovanni di Dio Fatebenefratelli - Brescia
  • University of Geneva
  • University of Eastern Finland
  • University of Barcelona
  • IRCSS San Martino University Hospital and IST
  • Hacettepe University
  • Aristotle University of Thessaloniki
  • Catholic University of the Sacred Heart
  • Lund University

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Cerebrospinal fluid (CSF) biomarkers may support the diagnosis of Alzheimer's disease (AD). We studied if the diagnostic power of AD CSF biomarker concentrations, i.e., Aβ42, total tau (t-tau), and phosphorylated tau (p-tau), is affected by differences in lateral ventricular volume (VV), using CSF biomarker data and magnetic resonance imaging (MRI) scans of 730 subjects, from 13 European Memory Clinics. We developed a Matlab-algorithm for standardized automated segmentation analysis of T1 weighted MRI scans in SPM8 for determining VV, and computed its ratio with total intracranial volume (TIV) as proxy for total CSF volume. The diagnostic power of CSF biomarkers (and their combination), either corrected for VV/TIV ratio or not, was determined by ROC analysis. CSF Aβ42 levels inversely correlated to VV/TIV in the whole study population (Aβ42: r=-0.28; p<0.0001). For CSF t-tau and p-tau, this association only reached statistical significance in the combined MCI and AD group (t-tau: r=-0.15; p-tau: r=-0.13; both p<0.01). Correction for differences in VV/TIV improved the differentiation of AD versus controls based on CSF Aβ42 alone (AUC: 0.75 versus 0.81) or in combination with t-tau (AUC: 0.81 versus 0.91). In conclusion, differences in VV may be an important confounder in interpreting CSF Aβ42 levels.

Original languageEnglish
Pages (from-to)543-555
Number of pages13
JournalJournal of Alzheimer's Disease
Volume56
Issue number2
DOIs
Publication statusPublished - 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Alzheimer's disease
  • amyloid biomarkers
  • cerebrospinal fluid
  • lateral ventricles
  • tau protein

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