| Literature DB >> 30306396 |
Liara Rizzi1,2, Luciane Missiaggia3,4, Matheus Roriz-Cruz3,4.
Abstract
The purpose of the study was to determine whether Aβ1-42 and p-Tau181 cerebral spinal fluid (CSF) levels can predict progression from amnestic mild cognitive impairment (aMCI) to Alzheimer's disease dementia (ADD) in a 3-year follow-up study. All participants were evaluated blindly by a behavioral neurologist and a neuropsychologist, and classified according to the Petersen criteria for aMCI and according to the Clinical Dementia Rating (CDR) scale. Individuals were also submitted to lumbar puncture at baseline. Levels of Aβ1-42 and p-Tau181 were measured by immunoenzymatic assay. Values were adjusted for age and sex. Thirty-one of 33 (93.9%) participants completed follow-up. Approximately 39% of aMCI individuals progressed to ADD. The relative risk of developing ADD in those with Aβ1-42 CSF levels lower than 618.5 pg/mL was 17.4 times higher than in those whose levels were higher than 618.5 pg/mL (P = 0.003). p-Tau181 alone did not predict progression to ADD (P = 0.101). The relative risk in those with a p-Tau181/Aβ1-42 ratio higher than 0.135 was 5.7 times greater (P < 0.001). Aβ1-42 and p-Tau181 explained 40.1% of the verbal memory test subscore of the Consortium to Establish a Registry for Alzheimer's Disease (ΔCERADs) variance (P = 0.008). Aβ1-42 strongly predicted progression from aMCI to ADD. p-Tau181 alone, or its relation to Aβ1-42, was inferior than Aβ1-42 alone as a predictor of progression to ADD.Entities:
Keywords: Alzheimer’s disease; Amyloid protein; CSF biomarkers; MCI; Tau
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Year: 2018 PMID: 30306396 DOI: 10.1007/s12017-018-8516-8
Source DB: PubMed Journal: Neuromolecular Med ISSN: 1535-1084 Impact factor: 3.843