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Paraskevas. Neuroimmunol Neuroinflammation 2020;7:183-93           Neuroimmunology
               DOI: 10.20517/2347-8659.2019.008                             and Neuroinflammation




               Review                                                                        Open Access


               Cerebrospinal fluid biomarkers for cognitive
               disorders. An introductory overview


               George P. Paraskevas

               Division of Cognitive and Movement Disorders and Unit of Neurochemistry and Biological Markers, 1st Department of Neurology,
               National and Kapodistrian University of Athens, School of Medicine, Eginition Hospital, Athens 11528, Greece.
               Correspondence to: Dr. George P. Paraskevas, Division of Cognitive and Movement Disorders and Unit of Neurochemistry
               and Biological Markers, 1st Department of Neurology, National and Kapodistrian University of Athens, School of Medicine,
               Eginition Hospital, 72 Vas. Sophias Ave, Athens 11528, Greece. E-mail: geoprskvs44@gmail.com
               How to cite this article: Paraskevas GP. Cerebrospinal fluid biomarkers for cognitive disorders. An introductory overview.
               Neuroimmunol Neuroinflammation 2020;7:183-93. http://dx.doi.org/10.20517/2347-8659.2019.008
               Received: 13 Aug 2019    First Decision: 24 Dec 2019    Revised: 11 Mar 2020    Accepted: 18 Mar 2020    Available online: 24 Jun 2020

               Science Editor: George P. Paraskevas    Copy Editor: Jing-Wen Zhang    Production Editor: Tian Zhang

               Abstract
               The core (established) cerebrospinal fluid biomarkers of Alzheimer’s disease (AD), namely amyloid-beta
               peptide, total tau protein and phospho-tau protein, have become a part of the diagnostic workup of patients with
               cognitive disorders in many specialized centers, especially for ambiguous cases. Combined, these biomarkers can
               identify the presence or absence of an AD biochemical process with sensitivities and specificities approaching or
               exceeding 90% in both dementia and pre-dementia stages of AD. Thus, they have been incorporated in various
               sets of research or clinical diagnostic criteria and recommendations. Results that are atypical, incompatible with
               AD, or inconclusive may occur, necessitating the use of other cerebrospinal fluid or imaging biomarkers.

               Keywords: Cerebrospinal fluid, tau, phospho-tau, amyloid-beta, Alzheimer’s disease, alpha-synuclein, TDP-43,
               neurofilament light protein



               INTRODUCTION
               Almost 25 years after their first introduction, cerebrospinal fluid (CSF) biomarkers have become a part
               of the diagnostic workup of patients with cognitive disorders in many specialized centers. Furthermore,
               they provide neurochemical information about the disorder underlying each individual patient’s clinical
               presentation, which currently should be viewed as a biological process, sometimes starting many years
               prior to symptom onset and gradually evolving into a typical or atypical clinical phenotype. This paper
               provides an introductory, concise review, regarding the current status and future perspectives of CSF
               biomarker use.


                           © The Author(s) 2020. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
                sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long
                as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
                and indicate if changes were made.


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