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

Author:

van Waalwijk van Doorn Linda J.C.12,Ghafoorian Mohsen3,van Leijsen Esther M.C.1,Claassen Jurgen A.H.R.4,Arighi Andrea5,Bozzali Marco67,Cannas Jorge8,Cavedo Enrica910,Eusebi Paolo11,Farotti Lucia11,Fenoglio Chiara12,Fortea Juan1314,Frisoni Giovanni B.915,Galimberti Daniela512,Greco Viviana1617,Herukka Sanna-Kaisa18,Liu Yawu18,Lleó Alberto1314,de Mendonça Alexandre8,Nobili Flavio M.1920,Parnetti Lucilla11,Picco Agnese19,Pikkarainen Maria18,Salvadori Nicola11,Scarpini Elio512,Soininen Hilkka18,Tarducci Roberto11,Urbani Andrea1617,Vilaplana Eduard1314,Meulenbroek Olga4,Platel Bram3,Verbeek Marcel M.12,Kuiperij H. Bea12

Affiliation:

1. Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud Alzheimer Centre, Radboud University Medical Center, Nijmegen, the Netherlands

2. Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, the Netherlands

3. Department of Radiology and Nuclear Medicine, Radboud University Medical Center, Nijmegen, the Netherlands

4. Department of Geriatrics, Donders Institute for Brain, Cognition and Behaviour, Radboud Alzheimer Centre, Radboud University Medical Center, Nijmegen, the Netherlands

5. Fondazione IRCCS Ca’ Granda, Ospedale Policlinico, Milan, Italy

6. IRCCS Fondazione Santa Lucia, Rome, Italy

7. Department of Neuroscience, Brighton and Sussex Medical School, University of Sussex, Brighton, United Kingdom

8. Faculty of Medicine, University of Lisbon, Lisbon, Portugal

9. Laboratory of Epidemiology, Neuroimaging and Telemedicine, IRCCS San Giovanni di Dio Fatebenefratelli, Brescia, Italy

10. Sorbonne University, GRC n° 21, Alzheimer Precision Medicine (APM), AP-HP, Pitié-Salpêtrière Hospital, Boulevard de l’hôpital, Paris, France; Qynapse, Paris, France

11. Section of Neurology, Center for Memory Disturbances, University of Perugia, Perugia, Italy

12. University of Milan, Dino Ferrari Center, Milan, Italy

13. Sant Pau Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain

14. Center of Biomedical Investigation Network for Neurodegenerative Diseases (CIBERNED), Madrid, Spain

15. University Hospitals and University of Geneva, Geneva, Switzerland

16. Fondazione Policlinica Universitario “A. Gemelli” –IRCCS, Rome, Italy

17. Department of Basic Biotechnological Sciences, Intensivological and Perioperative Clinics, Università Cattolica, Rome, Italy

18. Department of Neurology, University of Eastern Finland and Kuopio University Hospital, Kuopio, Finland

19. Department of Neuroscience (DINOGMI), University of Genoa, Genoa, Italy

20. IRCCS Ospedale Policlinico San Martino, Genoa, Italy

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.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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