Evidence map›Paper›PMID 38334599›Full record

ArticleCells2024

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

Joanna Palade, Eric Alsop, Amanda Courtright-Lim, Michael Hsieh, Timothy G Whitsett, Douglas Galasko, Kendall Van Keuren-Jensen

Open access · goldAbstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Extracellular RNAs as Messengers and Early Biomarkers in Neurodegeneration.International journal of molecular sciences · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Joanna PaladeNeurogenomics Division, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.ORCID 0000-0002-6493-2582
Eric AlsopNeurogenomics Division, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.
Amanda Courtright-LimBiomedical Ethics Program, Mayo Clinic, Scottsdale, AZ 85259, USA.
Michael HsiehNeurogenomics Division, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.
Timothy G WhitsettNeurogenomics Division, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.
Douglas GalaskoDepartment of Neurosciences, San Diego and Shiley-Marcos Alzheimer's Disease Research Center, University of California, La Jolla, CA 92037, USA.
Kendall Van Keuren-JensenNeurogenomics Division, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.
Translational Genomics Research Institute · USMayo Clinic in Arizona · USUniversity of California San Diego · US

Funding

UCSD Shiley-Marcos Alzheimer's Disease Research Center P30P30AG062429 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DOUGLAS R GALASKO · 2019 to 2026
$34.9M
exRNA signatures Predict Outcomes after brain injuryUH3TR000891 · NCATS · TRANSLATIONAL GENOMICS RESEARCH INST · PI ADELSON, P. DAVID, HUENTELMAN, MATT · 2015 to 2017
$3.0M
NCATS NIH HHS UH3 TR000891NIA NIH HHS P30 AG062429NIH HHS UH3 TR000891
6 · The paper itself

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.

Indexed as

Alzheimer DiseaseExtracellular VesiclesBiomarkersBrainEarly DiagnosisHumansBiomarkersAlzheimer’s diseasebiomarkerextracellular vesiclemild cognitive impairmentplasmasmall RNA sequencing

Identifiers

PMID38334599
PMCPMC10854972
OpenAlexW4391136195

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.