| Literature DB >> 32123385 |
Shorena Janelidze1, Niklas Mattsson2,3,4, Sebastian Palmqvist2,3, Ruben Smith2,3, Thomas G Beach5, Geidy E Serrano5, Xiyun Chai6, Nicholas K Proctor6, Udo Eichenlaub7, Henrik Zetterberg8,9,10,11, Kaj Blennow8,9, Eric M Reiman12, Erik Stomrud2,13, Jeffrey L Dage6, Oskar Hansson14,15.
Abstract
Plasma phosphorylated tau181 (P-tau181) might be increased in Alzheimer's disease (AD), but its usefulness for differential diagnosis and prognosis is unclear. We studied plasma P-tau181 in three cohorts, with a total of 589 individuals, including cognitively unimpaired participants and patients with mild cognitive impairment (MCI), AD dementia and non-AD neurodegenerative diseases. Plasma P-tau181 was increased in preclinical AD and further increased at the MCI and dementia stages. It correlated with CSF P-tau181 and predicted positive Tau positron emission tomography (PET) scans (area under the curve (AUC) = 0.87-0.91 for different brain regions). Plasma P-tau181 differentiated AD dementia from non-AD neurodegenerative diseases with an accuracy similar to that of Tau PET and CSF P-tau181 (AUC = 0.94-0.98), and detected AD neuropathology in an autopsy-confirmed cohort. High plasma P-tau181 was associated with subsequent development of AD dementia in cognitively unimpaired and MCI subjects. In conclusion, plasma P-tau181 is a noninvasive diagnostic and prognostic biomarker of AD, which may be useful in clinical practice and trials.Entities:
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Year: 2020 PMID: 32123385 DOI: 10.1038/s41591-020-0755-1
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440