| Literature DB >> 28059783 |
Linda J C van Waalwijk van Doorn1,2, Juan D Gispert3,4,5, H Bea Kuiperij1,2, Jurgen A H R Claassen6, Andrea Arighi7, Inês Baldeiras8, Kaj Blennow9,10, Marco Bozzali11, Miguel Castelo-Branco12, Enrica Cavedo13, Derya D Emek-Savaş14, Erden Eren15, Paolo Eusebi16, Lucia Farotti16, Chiara Fenoglio7, Juan Fortea Ormaechea17, Yvonne Freund-Levi18,19, Giovanni B Frisoni20,21, Daniela Galimberti7, Sermin Genc15, Viviana Greco22, Harald Hampel13, Sanna-Kaisa Herukka23, Yawu Liu23, Albert Lladó24, Alberto Lleó17, Flavio M Nobili25, Kader K Oguz26, Lucilla Parnetti16, João Pereira11, Agnese Picco25, Maria Pikkarainen23, Catarina Resende de Oliveira8, Esen Saka26, Nicola Salvadori16, Raquel Sanchez-Valle24, Isabel Santana8, Elio Scarpini7, Philip Scheltens27,28, Hilkka Soininen23, Roberto Tarducci16, Charlotte Teunissen29, Magda Tsolaki30, Andrea Urbani22,31, Eduard Vilaplana17, Pieter Jelle Visser27,28,32, Asa K Wallin33, Görsev Yener34, José L Molinuevo3,24, Olga Meulenbroek6, Marcel M Verbeek1,2.
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.Entities:
Keywords: Alzheimer’s disease; amyloid biomarkers; cerebrospinal fluid; lateral ventricles; tau protein
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Year: 2017 PMID: 28059783 DOI: 10.3233/JAD-160668
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472