Evidence map›Paper›PMID 39334890›Full record

ArticleBiomolecules2024

Urinary Extracellular Vesicles for Non-Invasive Quantification of Principal Cell Damage in Kidney Transplant Recipients.

Per Svenningsen, Rima Maslauskiene, Yaseelan Palarasah, Inga A Bumblyte, Martin Tepel

Abstract read
In one paragraph

Article in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Per SvenningsenDepartment of Molecular Medicine, University of Southern Denmark, 5230 Odense, Denmark.ORCID 0000-0001-6590-7103
Rima MaslauskieneDepartment of Nephrology, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.ORCID 0000-0001-7122-5141
Yaseelan PalarasahDepartment of Molecular Medicine, University of Southern Denmark, 5230 Odense, Denmark.
Inga A BumblyteDepartment of Nephrology, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.
Martin TepelDepartment of Nephrology, Odense University Hospital, 5000 Odense, Denmark.

Funding

Innovation Fund Denmark na
6 · The paper itself

Abstract

The objective of the present study was to compare principal cell-specific aquaporin-2 (AQP2) abundances in urinary extracellular vesicles (uEVs) on the first postoperative day in deceased-donor kidney transplant recipients without and with acute kidney injury. We measured uEV markers (CD9 and CD63) and the abundances of proximal tubular sodium-glucose transporter 2, distal tubular sodium/chloride cotransporter, and principal cell-specific aquaporin-2 using Western blotting of urine. uEV-AQP2 levels were normalized to living donor controls. The validation cohort consisted of 82 deceased-donor kidney transplant recipients who had a median age of 50 years (IQR 43 to 57 years). A total of 32% of recipients had acute kidney injury. The median uEV-AQP2 was significantly higher in recipients with acute kidney injury compared to immediate allograft function (2.05; IQR 0.87 to 2.83; vs. 0.81; IQR 0.44 to 1.78;

Indexed as

Aquaporin 2Extracellular VesiclesKidney TransplantationTetraspanin 29Acute Kidney InjuryAdultBiomarkersFemaleHumansMaleMiddle AgedTetraspanin 30Transplant RecipientsAQP2 protein, humanAquaporin 2BiomarkersCD63 protein, humanCD9 protein, humanTetraspanin 29Tetraspanin 30allograft injuryaquaporin-2 abundancedamage of principal cellsexosomesextracellular vesicleskidney transplanturinary extracellular vesicle

Identifiers

PMID39334890
PMCPMC11430813

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Registered trials

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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.