CSF and plasma biomarkers in cerebral amyloid angiopathy: A single-center study and a systematic review/meta-analysis

Author:

Theodorou Aikaterini1,Tsantzali Ioanna1,Stefanou Maria-Ioanna1,Sacco Simona2ORCID,Katsanos Aristeidis H3ORCID,Shoamanesh Ashkan3ORCID,Karapanayiotides Theodoros4,Koutroulou Ioanna4,Stamati Polyxeni5,Werring David J6,Cordonnier Charlotte7,Palaiodimou Lina1ORCID,Zompola Christina1,Boviatsis Efstathios8,Stavrinou Lampis8,Frantzeskaki Frantzeska9,Steiner Thorsten10,Alexandrov Andrei V11,Paraskevas Georgios P1,Tsivgoulis Georgios112ORCID

Affiliation:

1. Second Department of Neurology, “Attikon” University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

2. Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, Via Vetoio, Italy

3. Division of Neurology, McMaster University/Population Health Research Institute, Hamilton, Canada

4. Second Department of Neurology, Aristotle University of Thessaloniki, School of Medicine, AHEPA University Hospital, Thessaloniki, Greece

5. Department of Neurology, Laboratory of Neurogenetics, University of Thessaly, University Hospital of Larissa, Biopolis, Mezourlo Hill, Larissa, Greece

6. Stroke Research Centre, UCL Queen Square Institute of Neurology, London, UK

7. University Lille, Inserm, CHU Lille, U1172, LilNCog, Lille Neuroscience and Cognition, France

8. Second Department of Neurosurgery, “Attikon” University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

9. Second Critical Care Department, “Attikon” University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

10. Departments of Neurology, Klinikum Frankfurt Höchst, Frankfurt and Heidelberg University Hospital, Heidelberg, Germany

11. Department of Neurology, University of Arizona, Banner University Medical Center, Phoenix

12. Department of Neurology, University of Tennessee Health Science Center, Memphis

Abstract

Introduction: There are limited data regarding cerebrospinal fluid (CSF) and plasma biomarkers among patients with Cerebral Amyloid Angiopathy (CAA). We sought to investigate the levels of four biomarkers [β-amyloids (Aβ42 and Aβ40), total tau (tau) and phosphorylated tau (p-tau)] in CAA patients compared to healthy controls (HC) and patients with Alzheimer Disease (AD). Patients and methods: A systematic review and meta-analysis of published studies, including also a 5 year single-center cohort study, with available data on CSF and plasma biomarkers in symptomatic sporadic CAA versus HC and AD was conducted. Biomarkers’ comparisons were investigated using random-effects models based on the ratio of mean (RoM) biomarker concentrations. RoM < 1 and RoM > 1 indicate lower and higher biomarker concentration in CAA compared to another population, respectively. Results: We identified nine cohorts, comprising 327 CAA patients (mean age: 71 ± 5 years; women: 45%) versus 336 HC (mean age: 65 ± 5 years; women: 45%) and 384 AD patients (mean age: 68 ± 3 years; women: 53%) with available data on CSF biomarkers. CSF Aβ42 levels [RoM: 0.47; 95% CI: 0.36–0.62; p < 0.0001], Aβ40 levels [RoM: 0.70; 95% CI: 0.63–0.79; p < 0.0001] and the ratio Aβ42/Aβ40 [RoM: 0.62; 95% CI: 0.39–0.98; p = 0.0438] differentiated CAA from HC. CSF Aβ40 levels [RoM: 0.73; 95% CI: 0.64–0.83; p = 0.0003] differentiated CAA from AD. CSF tau and p-tau levels differentiated CAA from HC [RoM: 1.71; 95% CI: 1.41–2.09; p = 0.0002 and RoM: 1.44; 95% CI: 1.20–1.73; p = 0.0014, respectively] and from AD [RoM: 0.65; 95% CI: 0.58–0.72; p < 0.0001 and RoM: 0.64; 95% CI: 0.57–0.71; p < 0.0001, respectively]. Plasma Aβ42 [RoM: 1.14; 95% CI: 0.89–1.45; p = 0.2079] and Aβ40 [RoM: 1.07; 95% CI: 0.91–1.25; p = 0.3306] levels were comparable between CAA and HC. Conclusions: CAA is characterized by a distinct CSF biomarker pattern compared to HC and AD. CSF Aβ40 levels are lower in CAA compared to HC and AD, while tau and p-tau levels are higher in CAA compared to HC, but lower in comparison to AD patients.

Publisher

SAGE Publications

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