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Cardiovascular effects of incretin-based drugs in patients with and without a history of heart failure: a protocol for a systematic review, meta-analysis and trial sequential analysis of randomised controlled trials.

BMJ open
January 1, 1970
Mohammed El-Sheikh et al. (8 authors)
Journal ArticleHuman Study
Extracted Claims (12)
InterventionDirectionEndpointPopulationDosageImpactClaim #
incretin-based drugs, including glucagon-like peptide-1 (GLP-1) receptor agonists (RAs) and dual glucose-dependent insulinotropic polypeptide (GIP)/GLP-1 RAs
increase
cardiovascular outcomes
patients with type 2 diabetes mellitus and obesity
-
have shown cardiovascular benefits
#1
incretin-based drugs, including glucagon-like peptide-1 (GLP-1) receptor agonists (RAs) and dual glucose-dependent insulinotropic polypeptide (GIP)/GLP-1 RAs
no change
cardiac structure and function
patients with and without a history of heart failure (HF)
-
effects remain uncertain
#2
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
cardiovascular mortality
patients with and without a history of HF
-
effects
#3
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
HF hospitalisation
patients with and without a history of HF
-
effects
#4
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
myocardial infarction
patients with and without a history of HF
-
effects
#5
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
stroke
patients with and without a history of HF
-
effects
#6
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
heart rate
patients with and without a history of HF
-
effects
#7
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
systolic blood pressure
patients with and without a history of HF
-
effects
#8
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
N-terminal pro B-type natriuretic peptide
patients with and without a history of HF
-
effects
#9
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
left ventricular ejection fraction
patients with and without a history of HF
-
effects
#10
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
left ventricular end-diastolic volume
patients with and without a history of HF
-
effects
#11
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide
neutral
left ventricular end-systolic volume
patients with and without a history of HF
-
effects
#12
Abstract

BACKGROUND: Incretin-based drugs, including glucagon-like peptide-1 (GLP-1) receptor agonists (RAs) and dual glucose-dependent insulinotropic polypeptide (GIP)/GLP-1 RAs, are increasingly used in the management of type 2 diabetes mellitus and obesity. While these agents have shown cardiovascular benefits, their effects on both cardiovascular outcomes and cardiac structure and function remain uncertain-particularly in patients with and without a history of heart failure (HF). METHODS AND ANALYSIS: We will conduct a systematic review and search major medical databases (Cochrane Central Register of Controlled Trials (CENTRAL), Medical Literature Analysis and Retrieval System Online (MEDLINE), Excerpta Medica Database (EMBASE), Latin American and Caribbean Health Sciences Literature (LILACS), Science Citation Index Expanded (SCI-EXPANDED) and Conference Proceedings Citation Index-Science (CPCI-S)), as well as clinical trial registries from their inception and onwards to identify relevant randomised trials. The literature search is scheduled for July 2025. Two review authors will independently extract data and assess risk of bias. We will include randomised controlled trials assessing the effects of cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatide in patients with and without a history of HF. The primary outcome will be cardiovascular mortality. Secondary outcomes will include HF hospitalisation, myocardial infarction, stroke, heart rate, systolic blood pressure, N-terminal pro B-type natriuretic peptide, left ventricular ejection fraction, left ventricular end-diastolic volume and left ventricular end-systolic volume. Data will be synthesised by aggregate data meta-analyses and trial sequential analysis. Risk of bias will be assessed with the Cochrane Risk of Bias tool, version 2, and the certainty of the evidence will be assessed by Grading of Recommendations, Assessment, Development and Evaluations (GRADE). ETHICS AND DISSEMINATION: As this study is a systematic review based on secondary analysis of published data, ethical approval is not required. Findings will be published in international peer-reviewed scientific journals. PROSPERO REGISTRATION NUMBER: CRD420251003374.

Medical Subject Headings (MeSH)
HumansHeart FailureSystematic Reviews as TopicIncretinsRandomized Controlled Trials as TopicMeta-Analysis as TopicDiabetes Mellitus, Type 2Research DesignGlucagon-Like Peptide-1 Receptor Agonists
Study Links
PubMed ID40976663
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