Decision tree-based classification as a support to diagnosis in the Alzheimer's disease continuum using cerebrospinal fluid biomarkers: insights from automated analysis

OBJECTIVECerebrospinal fluid (CSF) biomarkers add accuracy to the diagnostic workup of cognitive impairment by illustrating Alzheimer's disease (AD) pathology. However, there are no universally accepted cutoff values for the interpretation of AD biomarkers. The aim of this study is to determine...

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Veröffentlicht in:Revista brasileira de psiquiatria 2022, Vol.44 (4), p.370-377
Hauptverfasser: Costa, Alana, Pais, Marcos, Loureiro, Júlia, Stella, Florindo, Radanovic, Márcia, Gattaz, Wagner, Forlenza, Orestes, Talib, Leda
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Sprache:eng
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Zusammenfassung:OBJECTIVECerebrospinal fluid (CSF) biomarkers add accuracy to the diagnostic workup of cognitive impairment by illustrating Alzheimer's disease (AD) pathology. However, there are no universally accepted cutoff values for the interpretation of AD biomarkers. The aim of this study is to determine the viability of a decision-tree method to analyse CSF biomarkers of AD as a support for clinical diagnosis. METHODSA decision-tree method (automated classification analysis) was applied to concentrations of AD biomarkers in CSF as a support for clinical diagnosis in older adults with or without cognitive impairment in a Brazilian cohort. In brief, 272 older adults (68 with AD, 122 with mild cognitive impairment [MCI], and 82 healthy controls) were assessed for CSF concentrations of Aß1-42, total-tau, and phosphorylated-tau using multiplexed Luminex assays; biomarker values were used to generate decision-tree algorithms (classification and regression tree) in the R statistical software environment. RESULTSThe best decision tree model had an accuracy of 74.65% to differentiate the three groups. Cluster analysis supported the combination of CSF biomarkers to differentiate AD and MCI vs. controls, suggesting the best cutoff values for each clinical condition. CONCLUSIONAutomated analyses of AD biomarkers provide valuable information to support the clinical diagnosis of MCI and AD in research settings.
ISSN:1516-4446
1809-452X
1809-452X
DOI:10.47626/1516-4446-2021-2277