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Impact of seed amplification assay and surface-enhanced Raman spectroscopy combined approach on the clinical diagnosis of Alzheimer’s disease

BACKGROUND: The current diagnosis of Alzheimer’s disease (AD) is based on a series of analyses which involve clinical, instrumental and laboratory findings. However, signs, symptoms and biomarker alterations observed in AD might overlap with other dementias, resulting in misdiagnosis. METHODS: Here...

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Detalles Bibliográficos
Autores principales: D’Andrea, Cristiano, Cazzaniga, Federico Angelo, Bistaffa, Edoardo, Barucci, Andrea, de Angelis, Marella, Banchelli, Martina, Farnesi, Edoardo, Polykretis, Panagis, Marzi, Chiara, Indaco, Antonio, Tiraboschi, Pietro, Giaccone, Giorgio, Matteini, Paolo, Moda, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337059/
https://www.ncbi.nlm.nih.gov/pubmed/37438825
http://dx.doi.org/10.1186/s40035-023-00367-9
Descripción
Sumario:BACKGROUND: The current diagnosis of Alzheimer’s disease (AD) is based on a series of analyses which involve clinical, instrumental and laboratory findings. However, signs, symptoms and biomarker alterations observed in AD might overlap with other dementias, resulting in misdiagnosis. METHODS: Here we describe a new diagnostic approach for AD which takes advantage of the boosted sensitivity in biomolecular detection, as allowed by seed amplification assay (SAA), combined with the unique specificity in biomolecular recognition, as provided by surface-enhanced Raman spectroscopy (SERS). RESULTS: The SAA-SERS approach supported by machine learning data analysis allowed efficient identification of pathological Aβ oligomers in the cerebrospinal fluid of patients with a clinical diagnosis of AD or mild cognitive impairment due to AD. CONCLUSIONS: Such analytical approach can be used to recognize disease features, thus allowing early stratification and selection of patients, which is fundamental in clinical treatments and pharmacological trials. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40035-023-00367-9.