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distinct
6 studies tagged distinct, dated 2014-03-12 to 2023-09-04. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- CSF and plasma Aβ42/40 across Alzheimer's disease continuum: comparison of two ultrasensitive Simoa® assays targeting distinct amyloid regions 2023-09-04
- Cognitively unimpaired individuals with a low burden of Aβ pathology have a distinct CSF biomarker profile 2021-07-27
- CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia 2019-12-31
Studies
6 studies carry this tag.
Date range
2014 to 2023
Top journals
- Alzheimer's research & therapy 2
- Brain : a journal of neurology 1
- Clinical chemistry and laboratory medicine 1
- Journal of Alzheimer's disease : JAD 1
- The FEBS journal 1
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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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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There are biologically meaningful Aβ-downstream effects in individuals with a low burden of Aβ pathology, while structural and functional changes are still subtle or absent.
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51/100
NDs share a CSF profile characterized by increased levels of CSF CHIT1, YKL-40, and GFAP, which likely reflects a common neuroinflammatory response to protein misfolding and aggregation.
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Serum NGAL levels are increased in DS and associated with distinct species of Aβ depending on the progression of dementia as diagnosed by baseline and follow-up clinical assessments.
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Fibrillar amyloid-β (Aβ) is the major constituent of senile plaques in the brain of patients with Alzheimer's disease (AD).
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Recent studies suggest that subcortical structures, including striatum, are vulnerable to amyloid-β accumulation and other neuropathological features in familial Alzheimer's disease due to autosomal dominant mutations.