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light-chain
9 studies tagged light-chain, dated 2013-05-29 to 2024-04-20. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Serum neurofilament light chain and inflammatory cytokines as biomarkers for early detection of mild cognitive impairment 2024-04-20
- Potential Utility of Plasma P-Tau and Neurofilament Light Chain as Surrogate Biomarkers for Preventive Clinical Trials 2023-03-06
- Plasma neurofilament light chain as a biomarker of Alzheimer's disease in Subjective Cognitive Decline and Mild Cognitive Impairment 2022-03-14
Studies
9 studies carry this tag.
Date range
2013 to 2024
Top journals
- Journal of neurology 2
- Alzheimer's & dementia (Amsterdam, Netherlands) 1
- Annals of neurology 1
- BMC neurology 1
- European journal of neurology 1
8 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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To investigate the association between serum neurofilament light chain (NfL) levels, inflammatory cytokines, and cognitive function to assess their utility in the early detection of mild cognitive impairment (MCI).
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Plasma p-tau181/NfL can potentially be used to monitor large-scale population interventions in CU individuals.
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Plasma NfL levels might be a promising biomarker for neurodegeneration to discriminate cognitive decline due to AD from other conditions causing cognitive impairment in prodromal stages.
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Our findings highlight the potential of serum NfL as a useful surrogate end point of disease severity in upcoming targeted treatments.
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αSyn-PMCA is almost invariably positive in the CSF of patients with PAF establishing this condition as α-synucleinopathy.
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Comparable performance of CSF and blood NfL in many groups demonstrates the promise of NfL as a noninvasive biomarker of neurodegeneration; however, its utility in clinically meaningful scenarios requires greater scrutiny.
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Due to the significant clinical overlap between frontotemporal lobar degeneration (FTLD) spectrum disorders and late-onset primary psychiatric disorders (PPD), diagnostic biomarkers reflecting the different underlying pathophysiologies are urgently needed.
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The diagnostic value of neurofilament light chain protein in neurodegenerative dementia diseases is still controversial.
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40/100
The marked NFL elevation in some but not all FTD cases is likely to reflect the different underlying pathologies.