Evidence map›Paper›PMID 41620770›Full record

ArticleAlzheimer's research & therapy2026

An RNA biomarker panel for the diagnosis of Alzheimer's disease from whole blood.

Sean Paz, Janet D Robishaw, Massimo Caputi

Abstract read
In one paragraph

Article in Alzheimer's research & therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Sean PazDepartment of Biomedical Science, Charles E Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL, USA.
Janet D RobishawCollege of Veterinary Medicine, University of Florida, Gainesville, FL, USA.
Massimo CaputiDepartment of Biomedical Science, Charles E Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL, USA. mcaputi@health.fau.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlzheimer’s Disease (AD) diagnosis remains primarily clinical, relying on patient history, cognitive tests, and sometimes brain imaging. Emerging approaches include advanced neuroimaging techniques and the use of protein biomarkers in cerebrospinal fluid and plasma. However, these methods have limitations such as high costs and the need for specialized infrastructures. In contrast, analysis of RNA expression in blood samples could be achieved with a high degree of sensitivity and accuracy in point of care settings, providing an ideal platform for a timely and accurate AD diagnosis.

methodsPeripheral blood samples from 50 AD patients and 50 healthy subjects were analyzed utilizing a whole transcriptome RNA sequencing approach to determine differences in the expression of (i) mRNAs, (ii) lncRNAs, (iii) miRNAs, (iv) circRNAs and (v) alternatively spliced mRNA isoforms. Multiple parallel analysis pipelines were utilized to identify a set of putative RNA biomarkers. A two-step validation assay was utilized to identify differentially expressed transcripts and form an AD RNA biomarker panel.

resultsThe final Alzheimer’s disease (AD) panel includes only mRNAs, as non-coding RNAs lacked sufficient robustness in whole blood for clinical translation under our criteria. Expression levels of the four selected RNA biomarkers in each AD patient were compared with those in healthy controls to calculate an AD predictive score (ADps), achieving a positive predictive value above 90% and specificity exceeding 95%.

conclusionsThe four RNA biomarkers can reliably identify Alzheimer’s disease (AD) patients using a small amount of peripheral blood and show strong potential as a minimally invasive, cost-effective tool for early diagnosis. However, their predictive accuracy and discriminative power may be more precisely established through analysis of a larger, well-defined AD cohort.

Indexed as

Alzheimer DiseaseRNAAgedAged, 80 and overBiomarkersFemaleHumansMaleMicroRNAsRNA, MessengerBiomarkersMicroRNAsRNARNA, MessengerAlzheimer’s diseaseRNATranscriptome.Whole blood

Identifiers

PMID41620770
PMCPMC12954934

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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.