Evidence map›Paper›PMID 34089496›Full record

ArticleCardiovascular toxicology2021

Empagliflozin Significantly Prevents the Doxorubicin-induced Acute Cardiotoxicity via Non-antioxidant Pathways.

Veysel Özgür Barış, Adnan Berk Dinçsoy, Esra Gedikli, Selim Zırh, Sevda Müftüoğlu, Ayşen Erdem

2 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in Cardiovascular toxicology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.7field-weighted citation impact, top 4% 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.

NCT06103279 phase2 / phase3unknown statusnot on this mapstarted 2023, after this paper: background citation

Evaluation of Empagliflozin Effect Against Doxorubicin Induced Cardiomyopathy

TypeinterventionalSponsorAin Shams UniversityRan2023 to 2024Enrolled40ConditionsCancerArmsEmpagliflozin 10 MG
NCT07070765 narecruitingnot on this mapstarted 2025, after this paper: background citation

Sodium-glucose Transporter Type 2 Inhibition in Anthracycline-related Cardiotoxicity - SPRINT

TypeinterventionalSponsorUniversity of AberdeenRan2025 to 2028Enrolled70ConditionsBreast CancerArmsSodium-glucose transport-2 (SGLT-2) inhibitors, Standard medical treatment
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 41 citations in OpenAlex.

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  18. Cancer and Heart Failure: Dangerous Liaisons.Journal of cardiovascular development and disease · 2024
    Review
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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

6 authors at 2 institutions in 1 country.

Veysel Özgür BarışDepartment of Cardiology, Dr. Ersin Arslan Research and Education Hospital, Gaziantep, Turkey. veyselozgurbaris@gmail.com.ORCID 0000-0002-3021-8612
Adnan Berk DinçsoyDepartment of Physiology, Faculty of Medicine, Hacettepe University, School of Medicine, Sihhiye, Ankara, Turkey.
Esra GedikliDepartment of Physiology, Faculty of Medicine, Hacettepe University, School of Medicine, Sihhiye, Ankara, Turkey.
Selim ZırhDepartment of Histology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Sevda MüftüoğluDepartment of Histology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Ayşen ErdemDepartment of Physiology, Faculty of Medicine, Hacettepe University, School of Medicine, Sihhiye, Ankara, Turkey.
Hacettepe University · TRGaziantep Children's Hospital · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Empagliflozin (EMPA) is a SGLT-2 inhibitor that has positive effects on cardiovascular outcomes. In this study, we aim to evaluate the possible protective effects of EMPA against doxorubicin (DOX)-induced acute cardiotoxicity. Non-diabetic Sprague-Dawley rats were randomized into four groups. The control group received serum physiologic (1 ml), the EMPA group received EMPA, the DOX group was administered cumulatively 18 mg/kg body weight DOX. The DOX+EMPA group was administered DOX and EMPA. In the DOX group, LVDED (P < 0.05) and LVSED (P < 0.01), QTc interval (P < 0.001), the ratio of karyolysis and karyorrhexis (P < 0.001) and infiltrative cell proliferation (P < 0.001) were found to be higher than; EF, FS and normal cell morphology were lower than the control group (P < 0.001). In the DOX+EMPA group, LVEDD (P < 0.05) and LVESD (P < 0.01) values, QTc interval (P < 0.001), karyolysis and karyorrhexis ratios (P < 0.001) and infiltrative cell proliferation were lower (P < 0.01); normal cell morphology and EF were higher compared to the DOX group (P < 0.001). Our results showed that empagliflozin significantly ameliorated DOX-induced acute cardiotoxicity.

Indexed as

Action PotentialsAnimalsBenzhydryl CompoundsCardiotoxicityCell ProliferationDisease Models, AnimalDoxorubicinGlucosidesHeart DiseasesHeart RateMaleMitochondria, HeartMyocytes, CardiacRatsRats, Sprague-DawleySodium-Glucose Transporter 2 InhibitorsBenzhydryl CompoundsDoxorubicinempagliflozinGlucosidesSodium-Glucose Transporter 2 InhibitorsCardiotoxicityDoxorubicinEmpagliflozinHeart failure

Identifiers

PMID34089496
OpenAlexW3165608311

What OpenQuestion holds

Textmetadata
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.