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lumipulse
7 studies tagged lumipulse, dated 2021-01-12 to 2024-08-22. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Plasma p-tau181 and amyloid markers in Alzheimer's disease: A comparison between Lumipulse and SIMOA 2024-08-22
- Assessment of the Correlation and Diagnostic Accuracy between Cerebrospinal Fluid and Plasma Alzheimer's Disease Biomarkers: A Comparison of the Lumipulse and Simoa Platforms 2024-04-23
- Diagnostic Accuracy of Plasma p-tau217 for Detecting Pathological Cerebrospinal Fluid Changes in Cognitively Unimpaired Subjects Using the Lumipulse Platform 2024-01-01
Studies
7 studies carry this tag.
Date range
2021 to 2024
Top journals
- Alzheimer's & dementia (Amsterdam, Netherlands) 1
- Alzheimer's research & therapy 1
- Annals of clinical and translational neurology 1
- Frontiers in aging neuroscience 1
- International journal of molecular sciences 1
7 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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47/100
One-hundred-thirthy-three participants, namely 55 A+T+N+ AD, 28 Neurodegenerative disorders (NDD) and 50 controls were enrolled for the study.
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We compared the clinical and analytical performance of Alzheimer's disease (AD) plasma biomarkers measured using the single-molecule array (Simoa) and Lumipulse platforms.
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Plasma p-tau217 measured using the Lumipulse platform shows promise as an accurate biomarker of preclinical AD pathology.
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CSF biomarkers measured with the LUMIPULSE system showed good agreement with amyloid PET imaging.
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Manual ELISA assays are the most commonly used methods for quantification of biomarkers; however, they often show inter- and intra-laboratory variability that limits their wide use.
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The Lumipulse platform provides comparable sensitivity and specificity to established CSF immunoassays in identifying pre-symptomatic AD pathology.
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Cognitive and neuropsychological scores differed significantly among the groups, with descending performance among CN>SCD>MCI>AD.