Evidence map›Paper›PMID 41602168›Full record

ArticleFrontiers in aging2025

RNA transcripts in salivary extracellular vesicle cargo isolated from aged populations.

Sicheng Wen, Chang Yu, Maxfield M G Kelsey, Mandy Pereira, Hannah Alaimo, Em Teixeira, Jenna Pracht, Lori A Daiello, Jonathan Drake, John M Sedivy and 3 more

Abstract read
In one paragraph

Article in Frontiers in aging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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. Novel Potential Risk Loci for Migraine in the Portuguese Population.International journal of molecular sciences · 2026
    Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Sicheng WenDepartment of Medicine, Division of Hematology/Oncology, Rhode Island Hospital, Brown University, Providence, RI, United States.
Chang YuDepartment of Biostatistics, Brown University School of Public Health, Providence, RI, United States.
Maxfield M G KelseyDepartment of Molecular Biology, Cell Biology, and Biochemistry, Brown Center on the Biology of Aging, Brown University, Providence, RI, United States.
Mandy PereiraDepartment of Medicine, Division of Hematology/Oncology, Rhode Island Hospital, Brown University, Providence, RI, United States.
Hannah AlaimoAlzheimer's Disease and Memory Disorders Center, Rhode Island Hospital, Providence, RI, United States.
Em TeixeiraAlzheimer's Disease and Memory Disorders Center, Rhode Island Hospital, Providence, RI, United States.
Jenna PrachtAlzheimer's Disease and Memory Disorders Center, Rhode Island Hospital, Providence, RI, United States.
Lori A DaielloAlzheimer's Disease and Memory Disorders Center, Rhode Island Hospital, Providence, RI, United States.
Jonathan DrakeAlzheimer's Disease and Memory Disorders Center, Rhode Island Hospital, Providence, RI, United States.
John M SedivyDepartment of Molecular Biology, Cell Biology, and Biochemistry, Brown Center on the Biology of Aging, Brown University, Providence, RI, United States.
Zhijin WuDepartment of Biostatistics, Brown University School of Public Health, Providence, RI, United States.
Peter QuesenberryDepartment of Medicine, Division of Hematology/Oncology, Rhode Island Hospital, Brown University, Providence, RI, United States.
Jill A KreilingDepartment of Molecular Biology, Cell Biology, and Biochemistry, Brown Center on the Biology of Aging, Brown University, Providence, RI, United States.

Funding

Somatic Activation of Retrotransposition: A New Molecular Mechanism of Aging?P01AG051449 · NIA · BROWN UNIVERSITY · PI John M Sedivy · 2016 to 2026
$30.4M
Stem Cells and AgingP30GM145500 · NIGMS · RHODE ISLAND HOSPITAL · PI PETER J. QUESENBERRY · 2023 to 2026
$6.0M
MECHANISMS OF REPLICATIVE SENESCENCE IN CELLSR01AG016694 · NIA · BROWN UNIVERSITY · PI SEDIVY, JOHN M · 1999 to 2024
$5.7M
Salivary Extracellular Vesicles as Biomarkers for Alzheimer's Disease and Related DisordersR01AG074284 · NIA · BROWN UNIVERSITY · PI Jill Kreiling, lori A daiello · 2022 to 2026
$3.9M
Defining molecular contributions of LINE-1 retrotransposons to AD / ADRDR01AG078925 · NIA · ROCKEFELLER UNIVERSITY · PI John LaCava, John M Sedivy · 2022 to 2026
$3.7M
SEM for serial block-face imagingS10OD023461 · OD · BROWN UNIVERSITY · PI CRETON, ROBBERT J · 2017 to 2017
$791k
NIA NIH HHS P01 AG051449NIA NIH HHS R01 AG016694NIA NIH HHS R01 AG074284NIA NIH HHS R01 AG078925NIGMS NIH HHS P30 GM145500NIH HHS S10 OD023461
6 · The paper itself

Abstract

Introduction: Human saliva contains numerous factors, including DNA, RNA, and protein, that may reflect the health status of the individual. Many of these factors are contained within extracellular vesicles (EVs). The contents of EVs are thought to mirror the cytoplasm of the cell of origin, providing insight into the health of the cell. We investigated the RNA content from EVs isolated from saliva (salEVs) to determine if we could detect transcripts associated with neurodegenerative conditions. Methods: We characterized the RNA cargo of salEVs isolated from individuals over the age of 65 with normal cognition. The salEV RNA content was analyzed by RNA-seq and NanoString miRNA analysis. Results: We found approximately 48.4% of the reads mapped to the human genome, with the remainder mapping to prokaryotic genomes. The transcripts included protein-coding RNA, long non-coding RNA, retrotransposons, and miRNAs. A significant number of the protein-coding transcripts were associated with pathways involved in neurodegenerative conditions. In addition, there was an enrichment of transcripts containing AP-2ε, HEYL, HES4, and TCFL5 transcription factor binding sites. We found that the lncRNA content was similar between samples, with PCBP1-AS1, TEX41, and PVT1 being the top represented transcripts. There were 286 miRNAs found in the salEV samples. The pathways predicted to be affected by the top represented miRNAs include Hippo signaling, TGF-β signaling, Wnt signaling, FoxO signaling, ErbB signaling, axon guidance, and mTOR signaling. We could detect retrotransposon transcripts from LINE, SINE, and LTR elements in salEVs. When compared to blood-derived EVs, salEVs showed greater representation of transcripts associated with neurodegenerative pathways. Discussion: Our results indicate that salEVs contain transcripts that are associated with pathways involved in neurodegeneration. The presence of these transcripts in salEVs suggest that saliva may be used to screen for biomarkers of neurodegenerative diseases.

Indexed as

alzheimer’s diseasebiomarkerextracellular vesicleneurodegenerationRNA

Identifiers

PMID41602168
PMCPMC12832735

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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.