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Published in: Journal of Neurology 12/2015

01-12-2015 | Original Communication

Dissecting IWG-2 typical and atypical Alzheimer’s disease: insights from cerebrospinal fluid analysis

Authors: Ross W. Paterson, Jamie Toombs, Catherine F. Slattery, Jennifer M. Nicholas, Ulf Andreasson, Nadia K. Magdalinou, Kaj Blennow, Jason D. Warren, Cath J. Mummery, Martin N. Rossor, Michael P. Lunn, Sebastian J. Crutch, Nick C. Fox, Henrik Zetterberg, Jonathan M. Schott

Published in: Journal of Neurology | Issue 12/2015

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Abstract

Pathobiological factors underlying phenotypic diversity in Alzheimer’s disease (AD) are incompletely understood. We used an extended cerebrospinal fluid (CSF) panel to explore differences between “typical” with “atypical” AD and between amnestic, posterior cortical atrophy, logopenic aphasia and frontal variants. We included 97 subjects fulfilling International Working Group-2 research criteria for AD of whom 61 had “typical” AD and 36 “atypical” syndromes, and 30 controls. CSF biomarkers included total tau (T-tau), phosphorylated tau (P-tau), amyloid β1-42, amyloid βX-38/40/42, YKL-40, neurofilament light (NFL), and amyloid precursor proteins α and β. The typical and atypical groups were matched for age, sex, severity and rate of cognitive decline and had similar biomarker profiles, with the exception of NFL which was higher in the atypical group (p = 0.03). Sub-classifying the atypical group into its constituent clinical syndromes, posterior cortical atrophy was associated with the lowest T-tau [604.4 (436.8–675.8) pg/mL], P-tau (79.8 ± 21.8 pg/L), T-tau/Aβ1-42 ratio [2.3 (1.4–2.6)], AβX-40/X-42 ratio (22.1 ± 5.8) and rate of cognitive decline [1.9 (0.75–4.25) MMSE points/year]. Conversely, the frontal variant group had the highest levels of T-tau [1185.4 (591.7–1329.3) pg/mL], P-tau (116.4 ± 45.4 pg/L), T-tau/Aβ1-42 ratio [5.2 (3.3–6.9)] and AβX-40/X-42 ratio (27.9 ± 7.5), and rate of cognitive decline. Whilst on a group level IWG-2 “typical” and “atypical” AD share similar CSF profiles, which are very different from controls, atypical AD is a heterogeneous entity with evidence for subtle differences in amyloid processing and neurodegeneration between different clinical syndromes. These findings also have practical implications for the interpretation of clinical CSF biomarker results.
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Metadata
Title
Dissecting IWG-2 typical and atypical Alzheimer’s disease: insights from cerebrospinal fluid analysis
Authors
Ross W. Paterson
Jamie Toombs
Catherine F. Slattery
Jennifer M. Nicholas
Ulf Andreasson
Nadia K. Magdalinou
Kaj Blennow
Jason D. Warren
Cath J. Mummery
Martin N. Rossor
Michael P. Lunn
Sebastian J. Crutch
Nick C. Fox
Henrik Zetterberg
Jonathan M. Schott
Publication date
01-12-2015
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 12/2015
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-015-7904-3

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