Evidence map›Paper›PMID 30371149›Full record

ArticleJournal of the American Heart Association2018

Vitamin D Attenuates Endothelial Dysfunction in Uremic Rats and Maintains Human Endothelial Stability.

Marc Vila Cuenca, Evelina Ferrantelli, Elisa Meinster, Stephan M Pouw, Igor Kovačević, Renee X de Menezes, Hans W Niessen, Robert H J Beelen, Peter L Hordijk, Marc G Vervloet

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

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  14. Vitamin D and Its Potential Benefit for the COVID-19 Pandemic.Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists · 2021
    Review
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  17. Most exposed: the endothelium in chronic kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2020
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Marc Vila Cuenca1 Department of Nephrology VU University Medical Center Amsterdam The Netherlands.
Evelina Ferrantelli3 Department of Molecular Cell Biology and Immunology VU University Medical Center Amsterdam The Netherlands.
Elisa Meinster4 Department of Pathology and Cardiac Surgery VU University Medical Center Amsterdam The Netherlands.
Stephan M Pouw3 Department of Molecular Cell Biology and Immunology VU University Medical Center Amsterdam The Netherlands.
Igor Kovačević2 Amsterdam Cardiovascular Sciences Amsterdam The Netherlands.
Renee X de Menezes6 Department of Epidemiology and Biostatistics VU University Medical Center Amsterdam The Netherlands.
Hans W Niessen2 Amsterdam Cardiovascular Sciences Amsterdam The Netherlands.
Robert H J Beelen3 Department of Molecular Cell Biology and Immunology VU University Medical Center Amsterdam The Netherlands.
Peter L Hordijk2 Amsterdam Cardiovascular Sciences Amsterdam The Netherlands.
Marc G Vervloet1 Department of Nephrology VU University Medical Center Amsterdam The Netherlands.
Amsterdam UMC Location VUmc · NLAmsterdam Neuroscience · NL

Funding

UT Southwestern O'Brien Kidney Research Core CenterP30DK079328 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI MOE, ORSON W · 2007 to 2021
$16.9M
NIDDK NIH HHS P30 DK079328
6 · The paper itself

Abstract

Background Dysfunctional endothelium may contribute to the development of cardiovascular complications in chronic kidney disease ( CKD ). Supplementation with active vitamin D has been proposed to have vasoprotective potential in CKD , not only by direct effects on the endothelium but also by an increment of α-Klotho. Here, we explored the capacity of the active vitamin D analogue paricalcitol to protect against uremia-induced endothelial damage and the extent to which this was dependent on increased α-Klotho concentrations. Methods and Results In a combined rat model of CKD with vitamin D deficiency, renal failure induced vascular permeability and endothelial-gap formation in thoracic aorta irrespective of baseline vitamin D, and this was attenuated by paricalcitol. Downregulation of renal and serum α-Klotho was found in the CKD model, which was not restored by paricalcitol. By measuring the real-time changes of the human endothelial barrier function, we found that paricalcitol effectively improved the recovery of endothelial integrity following the addition of the pro-permeability factor thrombin and the induction of a wound. Furthermore, immunofluorescence staining revealed that paricalcitol promoted vascular endothelial-cadherin-based cell-cell junctions and diminished F-actin stress fiber organization, preventing the formation of endothelial intracellular gaps. Conclusions Our results demonstrate that paricalcitol attenuates the CKD -induced endothelial damage in the thoracic aorta and directly mediates endothelial stability in vitro by enforcing cell-cell interactions.

Indexed as

ActinsAnimalsAorta, ThoracicCadherinsCapillary PermeabilityDisease Models, AnimalEndothelium, VascularErgocalciferolsGlucuronidaseHumansHuman Umbilical Vein Endothelial CellsIntercellular JunctionsKlotho ProteinsRatsRenal Insufficiency, ChronicStress FibersActinsCadherinsErgocalciferolsGlucuronidaseKlotho Proteinsparicalcitolchronic kidney diseaseendothelial dysfunctionKlothovitamin D

Identifiers

PMID30371149
PMCPMC6201442
OpenAlexW2891714678

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.