Laura Ibanez, United States of America

Washington University School of Medicine Psychiatry
I received a PhD in Biomedicine from the University of Barcelona, Spain and completed a postdoctoral fellowship under the mentorship of Dr. Carlos Cruchaga at Washington University School of Medicine in St. Louis (WUSM). Then, I joined the faculty at WUSM in 2020, where I am currently an Assistant Professor of Psychiatry at the NeuroGenomics and Informatics Center (NGI-Center). My research interests are focused on developing new minimally invasive tools for rapid and accurate diagnosis of neurodegenerative diseases to provide early detection and improve management. Currently, I am leading research into prediction of pre-symptomatic Alzheimer's and Parkinson's disease using plasma high-throughput RNAseq.

Presenter of 2 Presentations

PREDICTION OF ALZHEIMER DISEASE USING PLASMA RNA SEQUENCES

Session Name
Session Type
SYMPOSIUM
Date
12.03.2021, Friday
Session Time
08:00 - 10:00
Room
On Demand Symposia C
Lecture Time
08:15 - 08:30
Session Icon
On-Demand

Abstract

Aims

The aim of this study was to generate predictive models for AD using plasma cell-free RNA species at different stages of the disease.

Methods

We generated cfRNA-Sequence data from AD cases at CDR=1 (N=44) and controls (N=45) and applied standard quality control. Gene expression was quantified with Salmon and corrected by library complexity and log transformed prior to analysis. Genes known to be involved in AD and other neurodegenerative diseases (N=25) were used to create a predictive model using step-wise discriminant analysis in the CDR=1. APOE genotype was included in the model afterwards. The predictive power was tested in early (N=27) and pre-symptomatic (N=21) stages of the disease.

Results

Out of the 25 genes, eight were included in the predictive model after step-wise discriminant analysis. After inclusion of APOE genotype, the area under the ROC curve was 0.96, 0.99 and 0.82 for CDR=1, CDR=0.5 and pre-symptomatic stages respectively (Figure1).

figure1.png

Conclusions

Cell-free RNA is a promising minimally invasive biomarker for AD with an accuracy comparable to the one obtained using CSF biomarkers. This approach can provide a new screening tool for AD that can be used at population level and to evaluate disease-modifying therapies that target amyloid beta and tau.

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