Alzheimer's disease cerebrospinal fluid biomarkers predict cognitive decline in lewy body dementia
ABSTRACT Introduction Alzheimer's disease pathologies are common in dementia with Lewy bodies, but their clinical relevance is not clear. CSF biomarkers amyloid beta 1‐42, total tau, and tau phosphorylated at threonine 181 reflect Alzheimer's disease neuropathology antemortem. In PD, low C...
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Published in | Movement disorders Vol. 31; no. 8; pp. 1203 - 1208 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.08.2016
Wiley Subscription Services, Inc Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | ABSTRACT
Introduction
Alzheimer's disease pathologies are common in dementia with Lewy bodies, but their clinical relevance is not clear. CSF biomarkers amyloid beta 1‐42, total tau, and tau phosphorylated at threonine 181 reflect Alzheimer's disease neuropathology antemortem. In PD, low CSF amyloid beta 1‐42 predict long‐term cognitive decline, but little is known about these biomarkers as predictors for cognitive decline in Lewy body dementia. The aim of this study was to assess whether Alzheimer's disease CSF biomarkers predict cognitive decline in Lewy body dementia.
Methods
From a large European dementia with Lewy bodies multicenter study, we analyzed baseline Alzheimer's disease CSF biomarkers and serial MMSE (baseline and 1‐ and 2‐year follow‐up) in 100 patients with Lewy body dementia. Linear mixed‐effects analyses, adjusted for sex, age, baseline MMSE, and education, were performed to model the association between CSF biomarkers and rate of cognitive decline measured with MMSE. An Alzheimer's disease CSF profile was defined as pathological amyloid beta 1‐42 plus pathological total tau or phosphorylated tau.
Results
The Alzheimer's disease CSF profile, and pathological levels of amyloid beta 1‐42, were associated with a more rapid decline in MMSE (2.2 [P < 0.05] and 2.9 points difference [P < 0.01], respectively). Higher total tau values showed a trend toward association without statistical significance (2.0 points difference; P = 0.064), whereas phosphorylated tau was not associated with decline.
Conclusions
Reduced levels of CSF amyloid beta 1‐42 were associated with more rapid cognitive decline in Lewy body dementia patients. Future prospective studies should include larger samples, centralized CSF analyses, longer follow‐up, and biomarker‐pathology correlation. © 2016 International Parkinson and Movement Disorder Society |
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Bibliography: | istex:D58964D6D7D6162672675FDF688E186C8518D540 ArticleID:MDS26668 ark:/67375/WNG-V2X4KCTB-6 Full financial disclosures and author roles may be found in the online version of this article. Nothing to report. This article was published online on 14 June 2016. After online publication, the Acknowledgments were revised. This notice is included in the online and print versions to indicate that both have been corrected on 27 June 2016. Relevant conflicts of interest/financial disclosures Funding agencies This research has been partially funded by JNPD. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0885-3185 1531-8257 1531-8257 |
DOI: | 10.1002/mds.26668 |