Small RNA Changes in Plasma Have Potential for Early Diagnosis of Alzheimer’s Disease before Symptom Onset

Author:

Palade Joanna1ORCID,Alsop Eric1,Courtright-Lim Amanda2,Hsieh Michael1,Whitsett Timothy G.1,Galasko Douglas3,Van Keuren-Jensen Kendall1

Affiliation:

1. Neurogenomics Division, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA

2. Biomedical Ethics Program, Mayo Clinic, Scottsdale, AZ 85259, USA

3. Department of Neurosciences, San Diego and Shiley-Marcos Alzheimer’s Disease Research Center, University of California, La Jolla, CA 92037, USA

Abstract

Alzheimer’s disease (AD), due to its multifactorial nature and complex etiology, poses challenges for research, diagnosis, and treatment, and impacts millions worldwide. To address the need for minimally invasive, repeatable measures that aid in AD diagnosis and progression monitoring, studies leveraging RNAs associated with extracellular vesicles (EVs) in human biofluids have revealed AD-associated changes. However, the validation of AD biomarkers has suffered from the collection of samples from differing points in the disease time course or a lack of confirmed AD diagnoses. Here, we integrate clinical diagnosis and postmortem pathology data to form more accurate experimental groups and use small RNA sequencing to show that EVs from plasma can serve as a potential source of RNAs that reflect disease-related changes. Importantly, we demonstrated that these changes are identifiable in the EVs of preclinical patients, years before symptom manifestation, and that machine learning models based on differentially expressed RNAs can help predict disease conversion or progression. This research offers critical insight into early disease biomarkers and underscores the significance of accounting for disease progression and pathology in human AD studies.

Funder

Michael J. Fox Foundation

National Institute of Health

Publisher

MDPI AG

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