Evidence map›Paper›PMID 38136567›Full record

ReviewBiomolecules2023

Beyond the Cardiovascular Effects of Glucagon-like Peptide-1 Receptor Agonists: Body Slimming and Plaque Stabilization. Are New Statins Born?

Dalgisio Lecis, Francesca Romana Prandi, Lucy Barone, Martina Belli, Domenico Sergi, Susanna Longo, Saverio Muscoli, Francesco Romeo, Massimo Federici, Stamatios Lerakis and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
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.

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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. 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 3 institutions in 2 countries.

Dalgisio LecisDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.
Francesca Romana PrandiDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0003-1878-8871
Lucy BaroneDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0001-9476-9168
Martina BelliDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0003-3648-9277
Domenico SergiDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.
Susanna LongoDepartment of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.
Saverio MuscoliDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0002-4037-7561
Francesco RomeoFaculty of Medicine, UniCamillus-Saint Camillus International University of Health and Medical Sciences, 00131 Rome, Italy.
Massimo FedericiDepartment of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.
Stamatios LerakisDivision of Cardiology, Mount Sinai Hospital, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, New York, NY 10029, USA.
Francesco BarillàDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.
University of Rome Tor Vergata · ITMount Sinai Hospital · USSaint Camillus International University of Health and Medical Sciences · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atherosclerosis is a chronic inflammatory disease characterized by lipid and inflammatory cell deposits in the inner layer of large- and medium-sized elastic and muscular arteries. Diabetes mellitus (DM) significantly increases the risk of cardiovascular diseases and the overall and cardiovascular mortality, and it is a pro-atherogenic factor that induces atherosclerosis development and/or accelerates its progression through a multifactorial process. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are a new class of drugs, belonging to the armamentarium to fight type 2 DM, that have shown robust reductions in atherosclerotic events and all-cause mortality in all studies. Preclinical studies have shown that GLP-1RAs play a role in the immunomodulation of atherosclerosis, affecting multiple pathways involved in plaque development and progression. In this review, we wanted to explore the translational power of such preclinical studies by analyzing the most recent clinical trials investigating the atheroprotective effect of GLP-1RAs.

Indexed as

AtherosclerosisCardiovascular DiseasesDiabetes Mellitus, Type 2Hydroxymethylglutaryl-CoA Reductase InhibitorsGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsHumansHypoglycemic AgentsGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsHydroxymethylglutaryl-CoA Reductase InhibitorsHypoglycemic Agentsatherosclerosiscardiovascular diseasediabetes mellitusGLP-1RAsprevention

Identifiers

PMID38136567
PMCPMC10741698
OpenAlexW4388938779

What Socratic holds

Texttitle and abstract
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.