Evidence map›Paper›PMID 38275636›Full record

ReviewAntioxidants (Basel, Switzerland)2023

Anti-Inflammation and Anti-Oxidation: The Key to Unlocking the Cardiovascular Potential of SGLT2 Inhibitors and GLP1 Receptor Agonists.

Veronika A Myasoedova, Michele Bozzi, Vincenza Valerio, Donato Moschetta, Ilaria Massaiu, Valentina Rusconi, Daniele Di Napoli, Michele Ciccarelli, Valentina Parisi, Piergiuseppe Agostoni and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Antioxidants (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.4field-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

18 citing papers in PubMed, 27 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Veronika A MyasoedovaCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.ORCID 0000-0001-8414-5300
Michele BozziCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.
Vincenza ValerioCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.
Donato MoschettaCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.ORCID 0000-0002-7746-8539
Ilaria MassaiuCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.
Valentina RusconiCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.
Daniele Di NapoliDepartment of Medicine, Surgery and Dentistry, University of Salerno, 84084 Fisciano, Italy.
Michele CiccarelliDepartment of Medicine, Surgery and Dentistry, University of Salerno, 84084 Fisciano, Italy.ORCID 0000-0003-2379-1960
Valentina ParisiDepartment of Translational Medical Sciences, Federico II University, 80138 Naples, Italy.
Piergiuseppe AgostoniCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.
Stefano GenoveseCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.
Paolo PoggioCentro Cardiologico Monzino IRCCS, 20138 Milan, Italy.ORCID 0000-0002-7225-3379
Centro Cardiologico Monzino · ITUniversity of Salerno · ITFederico II University Hospital · IT

Funding

European Union - Next Generation EU - NRRP M6C2 - Investment 2.1 Enhancement and strengthening of biomedical research in the NHS PNRR-MAD-2022-12376009Fondazone Gigi & Pupa Ferrari ONLUS FPF-14Italian Ministry of Health Ricerca Corrente to Centro Cardiologico Monzino IRCCS
6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2DM) is a prevalent and complex metabolic disorder associated with various complications, including cardiovascular diseases. Sodium-glucose co-transporter 2 inhibitors (SGLT2i) and glucagon-like peptide 1 receptor agonists (GLP1-RA) have emerged as novel therapeutic agents for T2DM, primarily aiming to reduce blood glucose levels. However, recent investigations have unveiled their multifaceted effects, extending beyond their glucose-lowering effect. SGLT2i operate by inhibiting the SGLT2 receptor in the kidneys, facilitating the excretion of glucose through urine, leading to reduced blood glucose levels, while GLP1-RA mimic the action of the GLP1 hormone, stimulating glucose-dependent insulin secretion from pancreatic islets. Both SGLT2i and GLP1-RA have shown remarkable benefits in reducing major cardiovascular events in patients with and without T2DM. This comprehensive review explores the expanding horizons of SGLT2i and GLP1-RA in improving cardiovascular health. It delves into the latest research, highlighting the effects of these drugs on heart physiology and metabolism. By elucidating their diverse mechanisms of action and emerging evidence, this review aims to recapitulate the potential of SGLT2i and GLP1-RA as therapeutic options for cardiovascular health beyond their traditional role in managing T2DM.

Indexed as

cardio-metabolismepicardial adipose tissuefibrosisglucagon-like peptide 1 receptor agonistsinflammationoxidative stresssodium-glucose cotransporter 2 inhibitors

Identifiers

PMID38275636
PMCPMC10812629
OpenAlexW4389991782

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.