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Published on: September 20, 2018
Clinical Manifestations
Gabriela Tomé Oliveira Engelmann1,2,3, Giovanna Correia Pereira Moro1,2,4, Ivonne Carolina Bolaños Burgos5
1Older Adult's Psychiatry and Psychology Extension Program (PROEPSI), School of Medicine, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil.
Higher phosphorylated tau protein (p-Tau 181) levels correlate with poorer performance on memory and cognitive assessments in older adults. This finding aids in understanding Alzheimer's disease progression and risk factors.
Area of Science:
- Neuroscience
- Biomarker Research
- Gerontology
Background:
- Understanding Alzheimer's disease (AD) biomarkers and cognitive decline is crucial for identifying risk factors for dementia.
- The Dementia Rating Scale (DRS) assesses cognitive function, while cerebrospinal fluid (CSF) biomarkers like Aβ42 and p-Tau 181 indicate AD pathology.
Purpose of the Study:
- To investigate the association between CSF Aβ42, p-Tau 181 levels, and performance on the DRS in older adults.
- To determine if these biomarkers can predict cognitive decline and conversion to Alzheimer's Disease Dementia (ADD).
Main Methods:
- Sixty-four participants (Cognitively Unimpaired, Mild Cognitive Impairment, ADD) were analyzed.
- CSF Aβ42 and p-Tau 181 levels were measured using Luminex xMAP.
- Spearman correlation and adjusted linear regression analyses were performed to assess relationships between biomarkers and DRS performance.
Main Results:
- Elevated CSF p-Tau 181 levels significantly correlated with worse performance on DRS Memory and total scores (DRST).
- No significant correlation was observed between CSF Aβ42 and DRS performance.
- The p-Tau 181/Aβ42 ratio also showed a significant negative correlation with Memory and DRST scores.
Conclusions:
- Higher p-Tau 181 levels are associated with poorer cognitive function, particularly in memory, as measured by the DRS.
- This association persists even after adjusting for sociodemographic factors, highlighting p-Tau 181's potential as a predictive biomarker for cognitive decline in Alzheimer's disease.
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