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assay
14 studies tagged assay, dated 2017-07-12 to 2025-07-01. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Equivalence of Plasma and Serum for Clinical Measurement of p-tau217: Comparative Analyses of Four Blood-Based Assays 2025-07-01
- Biomarker discovery in Alzheimer's and neurodegenerative diseases using Nucleic Acid Linked Immuno-Sandwich Assay 2025-05-01
- A comparison of p-tau assays for the specificity to detect tau changes in Alzheimer's disease 2025-04-01
Studies
14 studies carry this tag.
Date range
2017 to 2025
Top journals
- Alzheimer's & dementia : the journal of the Alzheimer's Association 4
- Alzheimer's research & therapy 2
- Journal of Alzheimer's disease : JAD 2
- Clinical chemistry and laboratory medicine 1
- Diagnostics (Basel, Switzerland) 1
9 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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Phosphorylated tau (p-tau) 217 is a promising blood biomarker for Alzheimer's disease (AD).
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We underline the potential of next-generation biomarker identification tools to detect novel proteomic features that also incorporate established biomarkers.
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60/100
LMW-specific p-tau assays could be more useful in the diagnostic workup of AD, especially in population-based communities where conditions causing peripheral neuropathy are frequent.
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Alzheimer's disease (AD) is a progressive irreversible neurodegenerative disorder that represents a major global public health concern.
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Our results show that the measurement of p-Tau181 in plasma has great potential as a non-invasive prognostic screening tool for implementation in a clinical setting.
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This study demonstrated the utility of a blood-based, multi-pathway biomarker assay for early screening and staging of AD, providing insights for patient stratification and precision medicine.
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Differences observed in technical and diagnostic performance of the two assays may depend on matrix-specific amyloid processing, suggesting that further studies should be carried to standardize amyloid ratio measurement in plasma.
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This study suggests that plasma Aβ42/Aβ40, as determined by this MS-based assay, has potential value as an accurate and cost-effective tool to identify individuals in the earliest stages of AD, supporting its implementation in clinical trials, preventative strategies and clinical practice.
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Pathogenesis of presymptomatic disease stages remains elusive, although studies suggest that the early structural and functional alterations likely occur at neuronal dendritic spines.
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A lack of convenient and reliable biomarkers for diagnosis and prognosis is a common challenge for neurodegenerative diseases such as Alzheimer's disease (AD).
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Blood-based biomarker assays of plasma β-amyloid (Aβ) and tau have the advantages of cost-effective and less invasive for the diagnosis of Alzheimer's disease (AD).
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In this sample, the high-throughput blood Aβ assay was not able to distinguish well between AD patients and controls.
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This study confirms strong concordance between CSF biomarkers and PET Aβ-amyloid status is independent of immunoassay platform, supporting their utility as biomarkers in clinical practice for the diagnosis of AD and for participant enrichment in clinical trials.
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Assay drift may reduce statistical power or even confound analyses.