Evidence mapPaperPMID 42405333Full record

ArticleFrontiers in cell and developmental biology2026

Longitudinal changes in the phenotypic profile of circulating extracellular vesicles in healthy individuals.

Kirstine Kløve-Mogensen, Rikke Bæk, Rikke W Rasmussen, Evo K L Søndergaard, Aase Handberg, Maiken Mellergaard, Malene M Jørgensen

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In one paragraph

Article in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing 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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Kirstine Kløve-MogensenDepartment of Clinical Immunology, Aalborg University Hospital, Aalborg, Denmark.
Rikke BækDepartment of Clinical Immunology, Aalborg University Hospital, Aalborg, Denmark.
Rikke W RasmussenDepartment of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark.
Evo K L SøndergaardDepartment of Clinical Immunology, Aalborg University Hospital, Aalborg, Denmark.
Aase HandbergDepartment of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark.
Maiken MellergaardDepartment of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark.
Malene M JørgensenDepartment of Clinical Immunology, Aalborg University Hospital, Aalborg, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Extracellular vesicles (EVs) are emerging as valuable biomarkers in clinical diagnostics. Yet, the natural biological variation in EV concentration and phenotype among healthy individuals and across longitudinal time points remains insufficiently characterized, complicating interpretation and reproducibility in biomarker studies. Objective: To assess longitudinal (day-to-day and week-to-week) intra-individual and inter-individual variation in circulating EVs from healthy donors using complementary analytical platforms. Methods: Blood samples were collected longitudinally from four healthy female donors over 5 consecutive days and across 6 weeks. EVs were analyzed using nanoparticle tracking analysis (NTA), high-resolution flow cytometry (hFCM) targeting 3 surface markers, and the EV Array targeting 23 surface markers. Blood cell counts were also measured to explore correlations with EV profiles. Results: Significant longitudinal intra- and inter-individual variation was observed in EV concentrations and marker expression. CD9-positive EVs were consistently the most abundant across both antibody-based methods, while CD63 Conclusion: This exploratory study underscores the dynamic nature of EV profiles in healthy individuals and highlights the need for standardized reference ranges and harmonized methodologies. Without accounting for biological and technical variability, EV-based biomarker studies risk misinterpretation and compromised reproducibility.

Indexed as

day-to-day variationEV Arrayextracellular vesicleshigh-resolution flow cytometry hFCMlongitudinal changesphenotype

Identifiers

PMID42405333
PMCPMC13328366

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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 Socratic graph.