| Literature DB >> 28527630 |
Simone Lista1, Nicola Toschi2, Filippo Baldacci3, Henrik Zetterberg4, Kaj Blennow5, Ingo Kilimann6, Stefan J Teipel6, Enrica Cavedo7, Antonio Melo Dos Santos8, Stéphane Epelbaum8, Foudil Lamari9, Bruno Dubois8, Roberto Floris10, Francesco Garaci11, Harald Hampel12.
Abstract
We assessed the diagnostic accuracy of cerebrospinal fluid (CSF) neurofilament light chain (NFL) protein in the classification of patients with Alzheimer's disease (AD) and cognitively healthy control individuals (HCs) and patients with frontotemporal dementia (FTD) as comparisons. Particularly, we tested the performance of CSF NFL concentration in differentiating patient groups stratified by fluid biomarker profiles, independently of the severity of cognitive impairment (mild cognitive impairment (MCI) and AD dementia individuals), using a biomarker-guided descriptive classification system for AD. CSF NFL concentrations were examined in a multicenter cross-sectional study of 108 participants stratified in AD pathophysiology-negative (both CSF tau and the 42-amino acid-long amyloid-beta (Aβ) peptide (Aβ1-42)) (n = 15), tau pathology-positive only (n = 15), Aβ pathology-positive only (n = 13), AD pathophysiology-positive (n = 33), FTD (n = 9) patients, and HCs (n = 23), according to the biomarker-based classification system. The performance of CSF NFL in discriminating AD pathophysiology-positive patients from HCs is fair, whereas the ability in differentiating tau-positive patients from HCs is poor. The classificatory performance in distinguishing AD pathophysiology-positive patients from FTD is unsatisfactory.Entities:
Keywords: Alzheimer's disease pathophysiology; Biomarkers; Cerebrospinal fluid; Frontotemporal dementia; Mild cognitive impairment; Neurofilament light chain protein
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Year: 2017 PMID: 28527630 DOI: 10.1016/j.neuint.2017.05.010
Source DB: PubMed Journal: Neurochem Int ISSN: 0197-0186 Impact factor: 3.921