Alzheimer’s disease clinical decision points for two plasma p-tau217 laboratory developed tests in neuropathology confirmed samples DOI Creative Commons
Anna Mammel, Ging‐Yuek Robin Hsiung,

Ali Mousavi

и другие.

medRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Июль 29, 2024

ABSTRACT INTRODUCTION We evaluated the diagnostic performance of two commercial plasma p-tau217 immunoassays compared to CSF testing and neuropathology. METHODS 170 samples from University British Columbia Hospital Clinic for Alzheimer’s (AD) Related Disorders were analyzed using Fujirebio ALZpath assays. Decision points determined autopsy findings as standard. RESULTS had similar overall analytical clinical performance, with distinct decision each assay. Based on finding, both assays identified individuals AD other neurodegenerative diseases (ALZpath AUC = 0.94, AUC= 0.90). The assay detected pathology at milder disease stages DISCUSSION Our study reinforces utility an biomarker. Differences in test suggest specific approach is required practice.

Язык: Английский

Development of thresholds and a visualization tool for use of a blood test in routine clinical dementia practice DOI Creative Commons
Inge M.W. Verberk,

Jolien Jutte,

Maurice Y. Kingma

и другие.

Alzheimer s & Dementia, Год журнала: 2024, Номер 20(9), С. 6115 - 6132

Опубликована: Авг. 3, 2024

Abstract INTRODUCTION We developed a multimarker blood test result interpretation tool for the clinical dementia practice, including phosphorylated (P‐)tau181, amyloid‐beta (Abeta)42/40, glial fibrillary acidic protein (GFAP), and neurofilament light (NfL). METHODS measured plasma biomarkers with Simoa ( n = 1199), applied LASSO regression biomarker selection receiver operating characteristics (ROC) analyses to determine diagnostic accuracy. validated our findings in two independent cohorts constructed visualization approach. RESULTS P‐tau181, GFAP, NfL were selected. This combination had area under curve (AUC) 83% identify amyloid positivity pre‐dementia stages, AUC 87%–89% differentiate Alzheimer's or controls from frontotemporal dementia, 74%–76% Lewy bodies. Highly reproducible AUCs obtained cohorts. The resulting includes UpSet plots visualize stand‐alone results density combined. DISCUSSION Our is ready testing real‐world settings. Highlights practice. P‐tau, NfL. particularly useful diagnosis.

Язык: Английский

Процитировано

4

Influence of APOE ε4 on performance of CSF biomarkers in differentiating clinical Alzheimer's disease DOI Creative Commons
Yan Wang, Fangyu Li, Qi Qin

и другие.

The Journal of Prevention of Alzheimer s Disease, Год журнала: 2025, Номер unknown, С. 100065 - 100065

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Core blood biomarkers of Alzheimer's disease: A single-center real-world performance study DOI Creative Commons
Federico Emanuele Pozzi,

Elisa Conti,

Giulia Remoli

и другие.

The Journal of Prevention of Alzheimer s Disease, Год журнала: 2025, Номер 12(2), С. 100027 - 100027

Опубликована: Янв. 23, 2025

Язык: Английский

Процитировано

0

The value of serum glial fibrillary acidic protein as a biomarker of astrogliosis in different neurological diseases DOI
Luisa Agnello, Caterina Maria Gambino, Anna Maria Ciaccio

и другие.

Clinica Chimica Acta, Год журнала: 2025, Номер unknown, С. 120248 - 120248

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Alzheimer’s disease clinical decision points for two plasma p-tau217 laboratory developed tests in neuropathology confirmed samples DOI Creative Commons
Anna Mammel, Ging‐Yuek Robin Hsiung,

Ali Mousavi

и другие.

medRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Июль 29, 2024

ABSTRACT INTRODUCTION We evaluated the diagnostic performance of two commercial plasma p-tau217 immunoassays compared to CSF testing and neuropathology. METHODS 170 samples from University British Columbia Hospital Clinic for Alzheimer’s (AD) Related Disorders were analyzed using Fujirebio ALZpath assays. Decision points determined autopsy findings as standard. RESULTS had similar overall analytical clinical performance, with distinct decision each assay. Based on finding, both assays identified individuals AD other neurodegenerative diseases (ALZpath AUC = 0.94, AUC= 0.90). The assay detected pathology at milder disease stages DISCUSSION Our study reinforces utility an biomarker. Differences in test suggest specific approach is required practice.

Язык: Английский

Процитировано

0