Real-life reliability of plasma pTau181, A?(42)/A?(40), and pTau181/A?(42) measured by Lumipulse G600II in predicting cerebrospinal fluid amyloid status. in Journal of Alzheimer's disease : JAD / J Alzheimers Dis. 2025 Jan;103(1):305-315. doi: 10.1177/13872877241300315. Epub 2024 Dec 3.
2025
AO Cuneo
ASL Alessandria
ASL Cuneo 1
ASL Città di Torino
AO Cuneo
ASL Alessandria
ASL Cuneo 1
ASL Città di Torino
Tipo pubblicazione
Journal Article
Autori/Collaboratori (20)Vedi tutti...
Bozzali M
Dipartimento di Neuroscienze - Università di Torino, Ospedale Molinette, Torino, Italy.
Lopiano L
Dipartimento di Neuroscienze - Università di Torino, Ospedale Molinette, Torino, Italy.
Ferrandi D
SC Neurologia, Ospedale S. Croce, Moncalieri, Italy.
et alii...
Dipartimento di Neuroscienze - Università di Torino, Ospedale Molinette, Torino, Italy.
Lopiano L
Dipartimento di Neuroscienze - Università di Torino, Ospedale Molinette, Torino, Italy.
Ferrandi D
SC Neurologia, Ospedale S. Croce, Moncalieri, Italy.
et alii...
Abstract
BACKGROUND: Alzheimer's disease (AD) is the most common neurodegenerative dementia, with diagnosis traditionally reliant on clinical criteria. Cerebrospinal fluid (CSF) biomarkers like pTau181 and A?(42)/A?(40) ratio significantly improve diagnostic accuracy but are invasive. Plasma biomarkers measured by automated assays offer a non-invasive alternative. OBJECTIVE: To evaluate the diagnostic performance of plasma pTau181, A?(42)/A?(40), and pTau181/A?(42) ratios in predicting CSF amyloid status in a real-life clinical setting. METHODS: Data from consecutive patients whose plasma and CSF samples sent to our laboratory between March and October 2022, were retrospectively analyzed. Plasma and CSF pTau181, A?(42), and A?(40) levels were measured using the Lumipulse G600II platform. CSF amyloid status was classified as amyloid-positive (A+) or amyloid-negative (A-) based on the A?(42)/A?(40) ratio. Statistical analyses included Spearman correlation, receiver operating characteristic (ROC) curves, and multivariate logistic regression to evaluate biomarker performance. RESULTS: Among 165 individuals (83 females), 29.1% were classified as A+. Significant correlations were found between plasma and CSF biomarkers, with the highest for the pTau181/A?(42) ratio (?=0.620, p?0.0001). ROC analysis showed the pTau181/A?(42) ratio had the highest diagnostic performance (AUC 0.818), followed by pTau181 (AUC 0.794) and A?(42)/A?(40) (AUC 0.775). Combining plasma biomarkers in age-adjusted models improved diagnostic accuracy (AUC up to 0.846). CONCLUSIONS: Plasma biomarkers measured by the Lumipulse G600II platform show strong potential in predicting CSF amyloid status and possibly reduces the need for lumbar punctures. These findings support the potential use of plasma assays in the early diagnosis of AD. Anyway, further validations in larger multicenter cohorts are mandatory.
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PMID : 39623969
DOI : 10.1177/13872877241300315
Keywords
plasma; biomarkers; cerebrospinal fluid; Alzheimer's disease; Aged, 80 and over; ROC Curve; Reproducibility of Results; Biomarkers/blood/cerebrospinal fluid; Retrospective Studies; Middle Aged; Alzheimer Disease/blood/cerebrospinal fluid/diagnosis; Peptide Fragments/cerebrospinal fluid/blood; Aged; tau Proteins/cerebrospinal fluid/blood; Amyloid beta-Peptides/cerebrospinal fluid/blood; Male; Female; Humans;