Evidence map›Paper›PMID 34360539›Full record

ArticleInternational journal of molecular sciences2021

The Sodium-Glucose Cotransporter-2 Inhibitor Canagliflozin Alleviates Endothelial Dysfunction Following

Sevil Korkmaz-Icöz, Cenk Kocer, Alex A Sayour, Patricia Kraft, Mona I Benker, Sophia Abulizi, Adrian-Iustin Georgevici, Paige Brlecic, Tamás Radovits, Sivakkanan Loganathan and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05217654 (A Randomized, Double - Blind, Placebo - Controlled Trial to Investigate the Effect of Dapagliflozin on Ischemia Reperfusion Induced Endothelial Dysfunction of the Forearm Vasculature in Healthy Male Subjects), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 8% 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.

NCT05217654 phase1unknown statusnot on this mapstarted 2022, after this paper: background citation

A Randomized, Double - Blind, Placebo - Controlled Trial to Investigate the Effect of Dapagliflozin on Ischemia Reperfusion Induced Endothelial Dysfunction of the Forearm Vasculature in Healthy Male Subjects

TypeinterventionalSponsorMedical University of ViennaRan2022 to 2023Enrolled32ConditionsReperfusion Injury, Vascular ComplicationsArmsDapagliflozin 10mg, Placebo
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. SGLT2 Inhibition Ameliorates Age-Dependent Renovascular Rarefaction.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Protective Mechanisms of SGLTi in Ischemic Heart Disease.Journal of cardiovascular translational research · 2024
    Review
  9. Article
  10. Effects of hypoxia versus ischaemia on vascular functions of isolated rat thoracic aorta: revisiting theKardiochirurgia i torakochirurgia polska = Polish journal of cardio-thoracic surgery · 2023
    Article
  11. Editorial to theInternational journal of molecular sciences · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Graft Preservation Solution DuraGraftPharmaceuticals (Basel, Switzerland) · 2021
    Article
  17. Review
  18. 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

12 authors at 3 institutions in 2 countries.

Sevil Korkmaz-IcözDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Cenk KocerDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Alex A SayourDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Patricia KraftDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Mona I BenkerDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Sophia AbuliziDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Adrian-Iustin GeorgeviciDepartment of Anesthesiology, St. Josef Hospital, Ruhr-University Bochum, 44791 Bochum, Germany.ORCID 0000-0002-2710-2280
Paige BrlecicDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Tamás RadovitsHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
Sivakkanan LoganathanDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Matthias KarckDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Gábor SzabóDepartment of Cardiac Surgery, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Heidelberg University · DESemmelweis University · HUSt. Josef-Hospital · DE

Funding

Land Baden-Württemberg, Germany N/AMedical Faculty of the University of Heidelberg, Germany N/ANational Research, Development and Innovation Fund of Hungary, financed under the NVKP_16 funding scheme. Project no. NVKP_16-1-2016-0017 ('National Heart Program')National Research, Development and Innovation Office (NKFIH) of Hungary K134939Thematic Excellence Program (2020-4.1.1.-TKP2020) of the Ministry for Innovation and Technol-ogy in Hungary, within the framework of the Therapeutic Development and Bioimaging the-matic programs of the Semmelweis University N/A
6 · The paper itself

Abstract

Vascular ischemia/reperfusion injury (IRI) contributes to graft failure and adverse clinical outcomes following coronary artery bypass grafting. Sodium-glucose-cotransporter (SGLT)-2-inhibitors have been shown to protect against myocardial IRI, irrespective of diabetes. We hypothesized that adding canagliflozin (CANA) (an SGLT-2-inhibitor) to saline protects vascular grafts from IRI. Aortic rings from non-diabetic rats were isolated and immediately mounted in organ bath chambers (control, n = 9-10 rats) or underwent cold ischemic preservation in saline, supplemented either with a DMSO vehicle (IR, n = 8-10 rats) or 50µM CANA (IR + CANA, n = 9-11 rats). Vascular function was measured, the expression of 88 genes using PCR-array was analyzed, and feature selection using machine learning was applied. Impaired maximal vasorelaxation to acetylcholine in the IR-group compared to controls was significantly ameliorated by CANA (IR 31.7 ± 3.2% vs. IR + CANA 51.9 ± 2.5%,

Indexed as

AnimalsCanagliflozinEndothelium, VascularIn Vitro TechniquesMaleNeovascularization, PathologicRatsRats, WistarReperfusion InjurySodium-Glucose Transporter 2 InhibitorsVascular DiseasesVasodilationCanagliflozinSodium-Glucose Transporter 2 Inhibitorscanagliflozindiabetes mellitusendothelial functionischemia/reperfusionsodium-glucose cotransporter-2

Identifiers

PMID34360539
PMCPMC8345991
OpenAlexW3187047743

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.