Potential Value of Plasma Amyloid-β, Total Tau, and Neurofilament Light for Identification of Early Alzheimer's Disease
- PMID: 31145586
- DOI: 10.1021/acschemneuro.9b00095
Potential Value of Plasma Amyloid-β, Total Tau, and Neurofilament Light for Identification of Early Alzheimer's Disease
Abstract
The objective of the study was to explore the potential value of plasma indicators for identifying amnesic mild cognitive impairment (aMCI) and determine whether levels of plasma indicators are related to the performance of cognitive function and brain tissue volumes. In total, 155 participants (68 aMCI patients and 87 health controls) were recruited in the present cross-sectional study. The levels of plasma amyloid-β (Aβ) 40, Aβ42, total tau (t-tau), and neurofilament light (NFL) were measured using an ultrasensitive quantitative method. Machine learning algorithms were performed for establishing an optimal model of identifying aMCI. Compared with healthy controls, Aβ40 and Aβ42 levels were lower and NFL levels were higher in plasma of aMCI patients with an exception of t-tau levels. In aMCI patients, the higher plasma Aβ40 levels were correlated with the impaired episodic memory and negative correlations were observed between plasma t-tau levels and global cognitive function and gray matter (GM) volume. In addition, the higher plasma NFL levels were correlated with reduced hippocampus volume and total GM volume of the left inferior and middle temporal gyrus. An integrated model included clinical features, hippocampus volume, and plasma Aβ42 and NFL and had the highest accuracy for detecting aMCI patients (accuracy, 74.2%). We demonstrated that plasma Aβ40, Aβ42, t-tau, and NFL may be useful to identify aMCI and correlate with cognitive decline and brain atrophy. Among these plasma indicators, Aβ42 and NFL are more valuable as key members of a peripheral biomarker panel to detect aMCI.
Keywords: aMCI; machine learning; memory; plasma NFL; plasma amyloid-β; plasma t-tau.
Similar articles
-
Diagnostic and predictive power of plasma proteins in Alzheimer's disease: a cross-sectional and longitudinal study in China.Sci Rep. 2024 Jul 30;14(1):17557. doi: 10.1038/s41598-024-66195-7. Sci Rep. 2024. PMID: 39080359 Free PMC article.
-
Predicting Longitudinal Cognitive Decline and Alzheimer's Conversion in Mild Cognitive Impairment Patients Based on Plasma Biomarkers.Cells. 2024 Jun 22;13(13):1085. doi: 10.3390/cells13131085. Cells. 2024. PMID: 38994939 Free PMC article.
-
Stage-specific links between plasma neurofilament light and imaging biomarkers of Alzheimer's disease.Brain. 2020 Dec 1;143(12):3793-3804. doi: 10.1093/brain/awaa342. Brain. 2020. PMID: 33210117 Free PMC article.
-
Blood-based biomarkers for Alzheimer's disease in Down syndrome: A systematic review and meta-analysis.Alzheimers Dement. 2025 Apr;21(4):e70135. doi: 10.1002/alz.70135. Alzheimers Dement. 2025. PMID: 40219863 Free PMC article.
-
Predictive Accuracy of Blood-Derived Biomarkers for Amyloid-β Brain Deposition Along with the Alzheimer's Disease Continuum: A Systematic Review.J Alzheimers Dis. 2021;84(1):393-407. doi: 10.3233/JAD-210496. J Alzheimers Dis. 2021. PMID: 34542072
Cited by
-
Characterizing Plasma Biomarkers of Alzheimer's in a Diverse Community-Based Cohort: A Cross-Sectional Study of the HAB-HD Cohort.Front Neurol. 2022 Aug 18;13:871947. doi: 10.3389/fneur.2022.871947. eCollection 2022. Front Neurol. 2022. PMID: 36062019 Free PMC article.
-
Electroencephalography as a Non-Invasive Biomarker of Alzheimer's Disease: A Forgotten Candidate to Substitute CSF Molecules?Int J Mol Sci. 2021 Oct 8;22(19):10889. doi: 10.3390/ijms221910889. Int J Mol Sci. 2021. PMID: 34639229 Free PMC article. Review.
-
Correlations between cognitive reserve, gray matter, and cerebrospinal fluid volume in healthy elders and mild cognitive impairment patients.Front Neurol. 2024 Mar 1;15:1355546. doi: 10.3389/fneur.2024.1355546. eCollection 2024. Front Neurol. 2024. PMID: 38497043 Free PMC article.
-
Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals.Nat Commun. 2020 Nov 27;11(1):6024. doi: 10.1038/s41467-020-19543-w. Nat Commun. 2020. PMID: 33247134 Free PMC article.
-
Predicting AT(N) pathologies in Alzheimer's disease from blood-based proteomic data using neural networks.Front Aging Neurosci. 2022 Nov 29;14:1040001. doi: 10.3389/fnagi.2022.1040001. eCollection 2022. Front Aging Neurosci. 2022. PMID: 36523958 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical