Evidence mapPaperPMID 35628443Full record

ReviewInternational journal of molecular sciences2022

Role of Sodium-Glucose Co-Transporter 2 Inhibitors in the Regulation of Inflammatory Processes in Animal Models.

Sandra Feijóo-Bandín, Alana Aragón-Herrera, Manuel Otero-Santiago, Laura Anido-Varela, Sandra Moraña-Fernández, Estefanía Tarazón, Esther Roselló-Lletí, Manuel Portolés, Oreste Gualillo, José Ramón González-Juanatey and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  3. Observational
  4. Article
  5. Review
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  11. Late Allograft Loss and Contemporary Cardiorenal Metabolic Therapies.Journal of the American Society of Nephrology : JASN · 2025
    Review
  12. Review
  13. Article
  14. Anti-Inflammatory Effects of SGLT2 Inhibitors: Focus on Macrophages.International journal of molecular sciences · 2025
    Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. The Role of Inflammasomes in Heart Failure.International journal of molecular sciences · 2024
    Review
  20. 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

11 authors at 3 institutions in 1 country.

Sandra Feijóo-BandínCellular and Molecular Cardiology Research Unit, Institute of Biomedical Research (IDIS) and Xerencia de Xestión Integrada de Santiago de Compostela (XXIS/SERGAS), 15706 Santiago de Compostela, Spain.ORCID 0000-0002-3739-5806
Alana Aragón-HerreraCellular and Molecular Cardiology Research Unit, Institute of Biomedical Research (IDIS) and Xerencia de Xestión Integrada de Santiago de Compostela (XXIS/SERGAS), 15706 Santiago de Compostela, Spain.
Manuel Otero-SantiagoCellular and Molecular Cardiology Research Unit, Institute of Biomedical Research (IDIS) and Xerencia de Xestión Integrada de Santiago de Compostela (XXIS/SERGAS), 15706 Santiago de Compostela, Spain.
Laura Anido-VarelaCellular and Molecular Cardiology Research Unit, Institute of Biomedical Research (IDIS) and Xerencia de Xestión Integrada de Santiago de Compostela (XXIS/SERGAS), 15706 Santiago de Compostela, Spain.
Sandra Moraña-FernándezCellular and Molecular Cardiology Research Unit, Institute of Biomedical Research (IDIS) and Xerencia de Xestión Integrada de Santiago de Compostela (XXIS/SERGAS), 15706 Santiago de Compostela, Spain.
Estefanía TarazónCentro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), Institute of Health Carlos III, 28029 Madrid, Spain.ORCID 0000-0003-3466-2558
Esther Roselló-LletíCentro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), Institute of Health Carlos III, 28029 Madrid, Spain.
Manuel PortolésCentro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), Institute of Health Carlos III, 28029 Madrid, Spain.ORCID 0000-0002-4415-7160
Oreste GualilloLaboratory of Neuroendocrine Interactions in Rheumatology and Inflammatory Diseases, Institute of Biomedical Research (IDIS) and Xerencia de Xestión Integrada de Santiago de Compostela (XXIS/SERGAS), 15706 Santiago de Compostela, Spain.ORCID 0000-0002-7154-1328
José Ramón González-JuanateyCellular and Molecular Cardiology Research Unit, Institute of Biomedical Research (IDIS) and Xerencia de Xestión Integrada de Santiago de Compostela (XXIS/SERGAS), 15706 Santiago de Compostela, Spain.
Francisca LagoCellular and Molecular Cardiology Research Unit, Institute of Biomedical Research (IDIS) and Xerencia de Xestión Integrada de Santiago de Compostela (XXIS/SERGAS), 15706 Santiago de Compostela, Spain.
Instituto de Salud Carlos III · ESServicio Gallego de Salud · ESUniversidade de Santiago de Compostela · ES

Funding

Axencia Galega de Innovacion GPC IN607B 2021 108European Regional Development Fund (FEDER) and European Union framework MSCA-RISE-H2020 Programme Project number 734899Instituto de Salud Carlos III PI21/01145
6 · The paper itself

Abstract

Sodium-glucose co-transporter 2 inhibitors, also known as gliflozins, were developed as a novel class of anti-diabetic agents that promote glycosuria through the prevention of glucose reabsorption in the proximal tubule by sodium-glucose co-transporter 2. Beyond the regulation of glucose homeostasis, they resulted as being effective in different clinical trials in patients with heart failure, showing a strong cardio-renal protective effect in diabetic, but also in non-diabetic patients, which highlights the possible existence of other mechanisms through which gliflozins could be exerting their action. So far, different gliflozins have been approved for their therapeutic use in T2DM, heart failure, and diabetic kidney disease in different countries, all of them being diseases that have in common a deregulation of the inflammatory process associated with the pathology, which perpetuates and worsens the disease. This inflammatory deregulation has been observed in many other diseases, which led the scientific community to have a growing interest in the understanding of the biological processes that lead to or control inflammation deregulation in order to be able to identify potential therapeutic targets that could revert this situation and contribute to the amelioration of the disease. In this line, recent studies showed that gliflozins also act as an anti-inflammatory drug, and have been proposed as a useful strategy to treat other diseases linked to inflammation in addition to cardio-renal diseases, such as diabetes, obesity, atherosclerosis, or non-alcoholic fatty liver disease. In this work, we will review recent studies regarding the role of the main sodium-glucose co-transporter 2 inhibitors in the control of inflammation.

Indexed as

Diabetes Mellitus, Type 2Heart FailureSodium-Glucose Transporter 2 InhibitorsAnimalsGlucoseHumansInflammationModels, AnimalSodiumSodium-Glucose Transporter 2GlucoseSodiumSodium-Glucose Transporter 2Sodium-Glucose Transporter 2 InhibitorscytokinesinflammationM1/M2 macrophagesmetaflammationNLRP3 inflammasomepyroptosisSGLT2i

Identifiers

PMID35628443
PMCPMC9144929
OpenAlexW4280526551

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.