Evidence map›Paper›PMID 40741027›Full record

ArticleWorld journal of cardiology2025

Impact of glucagon-like peptide-1 receptor agonists on the incidence of atrial fibrillation.

Krzysztof Glaser, Wojciech Glaser, Luca Marino, Marek Ruchala, Federico Bilotta

Abstract read
In one paragraph

Article in World journal of cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

5 authors.

Krzysztof GlaserDepartment of Endocrinology, Metabolism and Internal Medicine, Poznan University of Medical Sciences, Poznan 60-355, Poland. glaser.krzysztof@gmail.com.
Wojciech GlaserFaculty of Medical Sciences, Medical University of Silesia, Katowice 40-055, Poland.
Luca MarinoDepartment of Mechanical and Aerospace Engineering, Sapienza University of Rome, Rome 00185, Italy.
Marek RuchalaDepartment of Endocrinology, Metabolism and Internal Medicine, Poznan University of Medical Sciences, Poznan 60-355, Poland.
Federico BilottaDepartment of Anesthesiology, Critical Care and Pain Medicine, Tor Vergata University, 00133 Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtrial fibrillation (AF) stands as the most prevalent type of arrhythmia, affecting approximately 60 million individuals world-wide. Although antiarrhythmic drugs (AADs) remain the gold standard for AF treatment, glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are arising as potential therapeutic alternatives.

aimTo evaluate the impact of GLP-1 RAs on the incidence of AF.

methodsInclusion criteria included systematic reviews (SRs) that based their analyses on clinical trials, observational studies, controlled trials and network meta-analyses. A total of 8 SRs were selected for data extraction, focusing on semaglutide, liraglutide and dulaglutide. Additionally, the effects of GLP-1 RAs on AF incidence were compared with those of sodium-glucose co-transporter 2 (SGLT2) inhibitors.

resultsFindings indicate that semaglutide, evaluated in the largest patient cohort across the 8 SRs, consistently reduced AF incidence. However, dulaglutide and liraglutide exhibited inconsistent effects. Notably, as opposed to variable outcomes associated with GLP-1 RAs, SGLT2 inhibitors a class of antidiabetic agents with weight-reducing properties exhibit significant cardiovascular benefits, including reductions in both AF and atrial flutter.

conclusionGLP-1 RAs emerge as a promising and potential alternative for AADs in reduction of incidence of AF. However, further research is required to fully determine their therapeutic potential and long-term cardiovascular effects.

Indexed as

Antiobesity medicationAtrial fibrillationDulaglutideGlucagon-like peptide-1 receptor agonistsLiraglutideSemaglutide

Identifiers

PMID40741027
PMCPMC12304861

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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.