Evidence map›Paper›PMID 37674992›Full record

ReviewFrontiers in nephrology2022

SGLT2 Inhibitors: A Broad Impact Therapeutic Option for the Nephrologist.

Antonio Granata, Francesco Pesce, Massimo Iacoviello, Massimiliano Anzaldi, Francesco Amico, Maria Catalano, Giuseppe Leonardi, Carmela Gatta, Giusy Costanza, Salvatore Corrao and 1 more

Open access · diamondAbstract readReview
In one paragraph

Review in Frontiers in nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
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 5 institutions in 1 country.

Antonio GranataNephrology and Dialysis Unit, "Cannizzaro" Emergency Hospital, Catania, Italy.
Francesco PesceRenal, Dialysis and Transplantation Unit, Department of Emergency and Organ Transplantation, University of Bari, Bari, Italy.
Massimo IacovielloCardiology Unit, Department of Medical and Surgical Science, University of Foggia, Foggia, Italy.
Massimiliano AnzaldiDiabetes Unit, "Cannizzaro" Emergency Hospital, Catania, Italy.
Francesco AmicoCardiology Unit, "Cannizzaro" Emergency Hospital, Catania, Italy.
Maria CatalanoCardiology Unit, "Cannizzaro" Emergency Hospital, Catania, Italy.
Giuseppe LeonardiCardiology Unit, Azienda Ospedaliera Universitaria (A.O.U.) "Policlinico-San Marco", Catania, Italy.
Carmela GattaInternal Medicine Unit, Azienda Ospedaliera Universitaria (A.O.U.) "Policlinico-San Marco", Catania, Italy.
Giusy CostanzaNephrology and Dialysis, "Vittorio Emanuele" Hospital, Gela, Italy.
Salvatore CorraoDepartment of Internal Medicine, "Azienda di Rilievo Nazionale ed Alta Specializzazione (ARNAS) Civico, Di Cristina e Benfratelli", Palermo, Italy.
Loreto GesualdoRenal, Dialysis and Transplantation Unit, Department of Emergency and Organ Transplantation, University of Bari, Bari, Italy.
Ospedale Cannizzaro · ITPoliclinico Universitario di Catania · ITUniversity of Bari Aldo Moro · ITAzienda di Rilievo Nazionale ed Alta Specializzazione · ITUniversity of Foggia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since their introduction as antidiabetic drugs, SGLT2 inhibitors (SGLT2i) have come a long way, proving to be beneficial on cardiovascular and renal outcomes independently of diabetes status. The benefits go far beyond glycemic control, and both the cardio- and nephroprotection are underpinned by diverse mechanisms. From the activation of tubule glomerular feedback and the consequent reduction in hyperfiltration to the improvement of hypoxia and oxidative stress in the renal cortex, SGLT2i have also been shown to inhibit hepcidin and limit podocyte damage. Likewise, they improve cardiac metabolism and bioenergetics, and reduce necrosis and cardiac fibrosis and the production of adipokines, cytokines, and epicardial adipose tissue mass. In terms of outcomes, the efficacy has been demonstrated on blood pressure control, BMI, albuminuria, stroke, heart disease, and mortality rate due to cardiovascular events. Patients with chronic kidney disease and proteinuria, with or without diabetes, treated with some SGLT2i have a reduced risk of progression. The analysis of subgroups of individuals with specific diseases such as IgA nephropathy has confirmed this solid effect on renal outcomes. Given these overarching activities on such a broad pathophysiological background and the favorable safety profile that goes with the use of SGLT2i, it is now certain that they are changing our approach to clinical interventions for important outcomes with an impressive impact.

Indexed as

CardioprotectionCKD - chronic kidney diseasediabetesglycemic controlNephro- protectionSGLT 2 inhibitors

Identifiers

PMID37674992
PMCPMC10479658
OpenAlexW4225116084

What OpenQuestion 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 OpenQuestion graph.