THE TAU, Aβ AND NFL BIOMARKERS IN THE PROGRESSION OF ALZHEIMER'S DISEASE
OS BIOMARCADORES TAU (Português (Brasil))

Keywords

Beta-amyloid; light chain neurofilament; insanity; plasma; atn

How to Cite

Tomé Oliveira Engelmann, G. (2021). THE TAU, Aβ AND NFL BIOMARKERS IN THE PROGRESSION OF ALZHEIMER’S DISEASE. Advanced Studies on Health and Nature, 1. Retrieved from https://periodicojs.com.br/index.php/easn/article/view/302

Abstract

Alzheimer's disease is the most frequent cause of dementia, characterized by an irreversible neurodegenerative process that mainly affects the elderly. Diagnosis detected early, as well as knowledge about the progression of the disease course, favors the choice of more assertive treatments and, consequently, allows greater well-being and quality of life for affected patients. However, currently, the invasiveness and high costs for its diagnosis become another barrier, not only for clinical performance, but also for studies that may come to elucidate the aspects that are still unclear about this disease. Therefore, this study sought to investigate blood biomarkers capable of detecting the progression of Alzheimer's disease through an integrative literature review with the identification of relevant productions on the subject. Data collection was performed using PubMed and Science Direct databases with the analysis of studies published from 2016 to 2021, related to the biomarkers Tau, beta-amyloid and light chain neurofilament. Among them, 8 works were selected according to the inclusion criteria established in this study. Thus, it is concluded that although the findings presented in the studies are relevant, to date there are no highly accurate biomarkers for detecting the progression of Alzheimer's disease, and further studies are needed to ensure a clear and consistent diagnosis.

OS BIOMARCADORES TAU (Português (Brasil))

References

ALTUNA-AZKARGORTA, M.; MENDIOROZ-IRIARTE, M. Blood biomarkers in Alzheimer’s disease. Neurología (English Edition), 2020.
ANDERSSON, Emelie et al. Blood and cerebrospinal fluid neurofilament light differentially detect neurodegeneration in early Alzheimer’s disease. Neurobiology of aging, v. 95, p. 143-153, 2020.
BACHMAN, Alvin H. et al. Change point analyses in prodromal Alzheimer's disease. Biomarkers in Neuropsychiatry, v. 3, p. 100028, 2020.
BEJANIN, Alexandre et al. Tau pathology and neurodegeneration contribute to cognitive impairment in Alzheimer’s disease. Brain, v. 140, n. 12, p. 3286-3300, 2017.
BRUNI, Amalia C.; BERNARDI, Livia; GABELLI, Carlo. From beta amyloid to altered proteostasis in Alzheimer’s disease. Ageing Research Reviews, p. 101126, 2020.
DE WOLF, Frank et al. Plasma tau, neurofilament light chain and amyloid-β levels and risk of dementia; a population-based cohort study. Brain, v. 143, n. 4, p. 1220-1232, 2020.
ERICA, Minos Kritikos Sean AP Clouston et al. Pathway Analysis for Plasma b-Amyloid, Tau and Neurofilament Light (ATN) in World Trade Center Responders at Midlife.
JANELIDZE, Shorena et al. Plasma β-amyloid in Alzheimer’s disease and vascular disease. Scientific reports, v. 6, n. 1, p. 1-11, 2016.
KAMETANI, Fuyuki; HASEGAWA, Masato. Reconsideration of amyloid hypothesis and tau hypothesis in Alzheimer’s disease. Frontiers in neuroscience, v. 12, p. 25, 2018.
KARIKARI, Thomas K. et al. Blood phosphorylated tau 181 as a biomarker for Alzheimer's disease: a diagnostic performance and prediction modelling study using data from four prospective cohorts. The Lancet Neurology, v. 19, n. 5, p. 422-433, 2020.
KHALIL, Michael et al. Neurofilaments as biomarkers in neurological disorders. Nature Reviews Neurology, v. 14, n. 10, p. 577-589, 2018.
LEWCZUK, Piotr et al. Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease. Alzheimer's research & therapy, v. 10, n. 1, p. 1-10, 2018.
MATTSSON, Niklas et al. Association of plasma neurofilament light with neurodegeneration in patients with Alzheimer disease. JAMA neurology, v. 74, n. 5, p. 557-566, 2017.
PALMQVIST, Sebastian et al. Discriminative accuracy of plasma phospho-tau217 for Alzheimer disease vs other neurodegenerative disorders. Jama, v. 324, n. 8, p. 772-781, 2020.
PHILIP, Scheltens et al. Van der Flier Wiesje Maria. Alzheimer's disease. The Lancet, v. 388, n. 10043, p. 505-517, 2016.
SCHULTZ, Stephanie A. et al. Serum neurofilament light chain levels are associated with white matter integrity in autosomal dominant Alzheimer's disease. Neurobiology of disease, v. 142, p. 104960, 2020.
SHIGEMOTO, Yoko et al. Gray matter structural networks related to 18F-THK5351 retention in cognitively normal older adults and early Alzheimer’s disease patients. Journal of Nuclear Medicine, v. 61, n. supplement 1, p. 604-604, 2020.
TIWARI, Sneham et al. Alzheimer’s disease: pathogenesis, diagnostics, and therapeutics. International journal of nanomedicine, v. 14, p. 5541, 2019.
YOUN, Young Chul et al. Blood amyloid-β oligomerization associated with neurodegeneration of Alzheimer’s disease. Alzheimer's research & therapy, v. 11, n. 1, p. 40, 2019.
ZETTERBERG, Henrik. Blood-based biomarkers for Alzheimer’s disease—An update. Journal of neuroscience methods, v. 319, p. 2-6, 2019.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...