White Matter Hyperintensities Are No Major Confounder for Alzheimer’s Disease Cerebrospinal Fluid Biomarkers

Linda Josephine Christine van Waalwijk van Doorn(Radboud University Nijmegen), Mohsen Ghafoorian(Radboud University Nijmegen), Esther M.C. van Leijsen(Radboud University Nijmegen), Jurgen A.H.R. Claassen(Radboud University Nijmegen), Andrea Arighi(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Marco Bozzali(Brighton and Sussex Medical School), Jorge Cannas(University of Lisbon), Enrica Cavedo(Sorbonne Université), Paolo Eusebi(University of Perugia), Lucia Farotti(University of Perugia), Chiara Fenoglio(University of Milan), Juan Fortea(Universitat Autònoma de Barcelona), Giovanni B. Frisoni(University of Geneva), Daniela Galimberti(University of Milan), Viviana Greco(Università Cattolica del Sacro Cuore), Sanna‐Kaisa Herukka(University of Eastern Finland), Yawu Liu(University of Eastern Finland), Alberto Lleó(Universitat Autònoma de Barcelona), Alexandre de Mendonça(University of Lisbon), Flavio Nobili(Ospedale Policlinico San Martino), Lucilla Parnetti(University of Perugia), Agnese Picco(University of Genoa), Maria Pikkarainen(University of Eastern Finland), Nicola Salvadori(University of Perugia), Elio Scarpini(University of Milan), Hilkka Soininen(University of Eastern Finland), R. Tarducci(University of Perugia), Andrea Urbani(Università Cattolica del Sacro Cuore), Eduard Vilaplana(Universitat Autònoma de Barcelona), Olga Meulenbroek(Radboud University Nijmegen), Bram Platel(Radboud University Nijmegen), Marcel M. Verbeek(Radboud University Nijmegen), H. Bea Kuiperij(Radboud University Nijmegen)
Journal of Alzheimer s Disease
November 24, 2020
Cited by 9Open Access
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Abstract

BACKGROUND: The cerebrospinal fluid (CSF) biomarkers amyloid-β 1-42 (Aβ42), total and phosphorylated tau (t-tau, p-tau) are increasingly used to assist in the clinical diagnosis of Alzheimer's disease (AD). However, CSF biomarker levels can be affected by confounding factors. OBJECTIVE: To investigate the association of white matter hyperintensities (WMHs) present in the brain with AD CSF biomarker levels. METHODS: We included CSF biomarker and magnetic resonance imaging (MRI) data of 172 subjects (52 controls, 72 mild cognitive impairment (MCI), and 48 AD patients) from 9 European Memory Clinics. A computer aided detection system for standardized automated segmentation of WMHs was used on MRI scans to determine WMH volumes. Association of WMH volume with AD CSF biomarkers was determined using linear regression analysis. RESULTS: A small, negative association of CSF Aβ42, but not p-tau and t-tau, levels with WMH volume was observed in the AD (r2 = 0.084, p = 0.046), but not the MCI and control groups, which was slightly increased when including the distance of WMHs to the ventricles in the analysis (r2 = 0.105, p = 0.025). Three global patterns of WMH distribution, either with 1) a low, 2) a peak close to the ventricles, or 3) a high, broadly-distributed WMH volume could be observed in brains of subjects in each diagnostic group. CONCLUSION: Despite an association of WMH volume with CSF Aβ42 levels in AD patients, the occurrence of WMHs is not accompanied by excess release of cellular proteins in the CSF, suggesting that WMHs are no major confounder for AD CSF biomarker assessment.


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