Plasma p-tau212 identifies cognitively unimpaired individuals with emerging amyloid-ß pathology
Przemysław R. Kac, Armand González Escalante, Marta Milà Alomà, Nicholas J. Ashton et autres
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Przemysław R. Kac, Armand González Escalante, Marta Milà Alomà, Nicholas J. Ashton et autres
Maciej Dulewicz, Przemysław R. Kac, Fernando C. Ortíz, Thomas K. Karikari et autres
Plasma biomarkers have emerged as promising less invasive alternatives for Alzheimer's disease (AD) detection. However, the diagnostic performance of phosphorylated tau (p-tau) isoforms remains incompletely validated. In a cohort of 160 patients from a memory clinic, plasma levels of p-tau217, p-tau212, p-tau181, …
se, pl, gb, de, us, cn, fr (code pays fourni par la source)
Maciej Dulewicz, Przemysław R. Kac, Fernando C. Ortíz, Thomas K. Karikari et autres
Fernando González‐Ortiz, Bjørn‐Eivind Kirsebom, Yara Yakoub, J Gundersen et autres
BACKGROUND AND OBJECTIVES: Aligning biomarker evidence with clinical presentation in early Alzheimer disease (AD) is essential for improving diagnosis, prognosis, and interventions. This study evaluates the relationship between cognitive impairment, future decline, and phosphorylated tau levels in plasma and CSF in predementia …
se, no, ca, gb, us, cn, fr (code pays fourni par la source)
Bjørn‐Eivind Kirsebom, Fernando González‐Ortiz, Sinthujah Vigneswaran, Geir Bråthen et autres
INTRODUCTION: Heterogeneity of clinical progression in Alzheimer's disease (AD) complicates the assessment of disease progression and treatment effects in trials. This study evaluates the potential of plasma phosphorylated tau-217 (p-tau217) to capture this heterogeneity. METHODS: We used k-means clustering to analyze cognitive …
no, se, nl, gb, cn, fr (code pays fourni par la source)
Przemysław R. Kac, Daniel Alcolea, Laia Montoliu‐Gaya, Susana Fernández et autres
BACKGROUND: All individuals with Down syndrome (DS) will develop full-blown Alzheimer´s disease (AD) pathology by age 40. Several genes encoded in chromosome 21, including dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A), have been proven to contribute to the pathology. Phosphorylation of tau at …
se, es, gb, no, us, cn, fr (code pays fourni par la source)
Cassandra Marotta, Fernando González‐Ortiz, Michael Turton, Henrik Zetterberg et autres
Abstract INTRODUCTION Brain‐derived tau (BD‐tau) measures tau specifically from brain‐derived sources and can differentiate Alzheimer's disease (AD) from other diseases. This study investigated BD‐tau as a potential biomarker of treatment effect. METHODS BD‐tau and phosphorylated tau‐217 (p‐tau217) levels were measured after treatment …
au, se, gb, hk (code pays fourni par la source)
Fernando González‐Ortiz, Jakub Vávra, Emma Payne, Bjørn‐Eivind Kirsebom et autres
Abstract Tau phosphorylation plays an important role in brain physiology and pathology. During foetal development, it supports microtubule dynamics and neuroplasticity, whereas in Alzheimer’s disease (AD), it drives pathological tau aggregation and tangle formation. In this multicentre study (n = 462), we …
se, us, au, in, no, es, gb, de, cn, fr (code pays fourni par la source)
Maciej Dulewicz, Przemysław R. Kac, Fernando González‐Ortiz, Thomas K. Karikari et autres
Abstract Background In the context of Alzheimer's disease (AD), blood‐based biomarkers have become increasingly important for various clinical purposes, such as screening patients and tracking the progression of the disease. Tau is a protein that stabilizes microtubules in nerve cells. In AD, …
se, us, pl, de, gb (code pays fourni par la source)
Przemysław R. Kac, Katheryn A Q Cousins, Leslie M. Shaw, David J. Irwin et autres
Abstract Background Phosphorylated‐tau (p‐tau) biomarkers are typically specific for Alzheimer’s disease (AD) and are less elevated in the cerebrospinal fluid (CSF) of frontotemporal lobar degeneration (FTLD) type tau (FTLD‐tau). FTLD is a pathologically and clinically heterogenous neurodegenerative disorder, and we currently lack …
se, us, gb (code pays fourni par la source)
Przemysław R. Kac, Daniel Alcolea, Laia Montoliu‐Gaya, Susana Fernández et autres
Background: All individuals with Down Syndrome (DS) will develop full-blown Alzheimeŕs disease (AD) pathology by age 40, decades before the occurrence of sporadic late-onset AD. Understanding this strong biological relation between age and AD pathology risk in DS is important to accelerate …
se, es, gb, no, us, cn, fr (code pays fourni par la source)
Fernando González‐Ortiz, Bjørn‐Eivind Kirsebom, Yara Yakoub, J Gundersen et autres
Abstract Background and objectives Detecting Alzheimer’s disease (AD) biological and clinical changes is crucial for early diagnostic and therapeutic interventions. Here we investigate the relationship between clinical severity and levels of phosphorylated tau, focusing on plasma biomarkers, in preclinical and prodromal AD. …
se, no, ca, gb, us, cn, fr (code pays fourni par la source)
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