4.7 Article

Added value of cerebrospinal fluid multimarker analysis in diagnosis and progression of dementia

Journal

EUROPEAN JOURNAL OF NEUROLOGY
Volume 28, Issue 4, Pages 1142-1152

Publisher

WILEY
DOI: 10.1111/ene.14658

Keywords

Alzheimer disease; amyloid; APOE; cerebrospinal fluid; positron emission tomography

Funding

  1. National Institutes of Health [K24HL148521, P30AG066511]

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By analyzing the accuracy of cerebrospinal fluid markers for Alzheimer disease (AD) and their impact on disease progression, it was found that combination of emerging/core AD markers can improve AD diagnosis, predict the conversion from mild cognitive impairment (MCI) into AD, and forecast a faster progression of dementia.
Background and purpose: Recently, some emerging cerebrospinal fluid (CSF) markers have been proposed as diagnostic tools for Alzheimer disease (AD) that can have an effect on disease progression. We analyze the accuracy of these CSF markers for diagnosis of AD in reference to brain amyloid positron emission tomography (PET). We also investigated whether they help in differentiating AD from other dementias and examined their influence in tracing the progression to dementia. Methods: Amyloid-beta (A beta) 1-42, total tau (t-tau), phosphorylated tau, A beta(40), A beta(38), beta-site amyloid precursor protein cleaving enzyme 1 (BACE-1), neurogranin (ng), phosphorylated neurofilament heavy-chain, and alpha-synuclein (alpha-syn) CSF levels were analyzed in 319 subjects, among whom 57 also underwent an amyloid PET scan. We also analyzed longitudinal clinical data from 239 subjects. Results: Emerging CSF markers, especially ng/BACE-1 ratio (area under the curve = 0.77) and their combinations with core AD CSF markers (all AUCs >0.85), showed high accuracy to discriminate amyloid PET positivity. Subjects with AD had higher CSF BACE-1, ng, and alpha-syn levels than those with non-AD dementia. CSF t-tau/alpha-syn ratio was higher in subjects with dementia with Lewy bodies than in those with frontotemporal dementia. Most emerging/core AD ratios predicted a faster conversion from mild cognitive impairment (MCI) stage to AD and appeared to be helpful when core AD CSF markers were discordant. In addition, the rate of cognitive decline was associated with all CSF core AD markers, several emerging/core AD two-marker ratios, and CSF ng levels. Conclusions: These results suggest that emerging biomarkers in conjunction with core AD markers improve diagnosis of AD, are associated with the conversion from MCI into AD, and predict a faster progression of dementia.

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