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16
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Evidence suggests Semaglutide maydecreaseMortality.

14 studies (18 claims)

Moderate consensus

Study Claims

16 of 19
InterventionDirectionEndpointTypePopulationDosageTitle
highly potent incretin receptor agonists semaglutide and tirzepatideDecreases - reduced riskpremature mortality
Human
patients with type 2 diabetes and obesityGLP-1 physiology in obesity and development of incretin-based drugs for chronic weight management.
GLP-1RAs semaglutide and tirzepatideDecreases - had a lower riskall-cause mortality
Human
adults with type 2 diabetes and obesityNeurodegeneration and Stroke After Semaglutide and Tirzepatide in Patients With Diabetes and Obesity.
GLP-1RAs semaglutide and tirzepatideDecreases - greater benefitsrisk of dementia, stroke, and all-cause mortality
Human
patients aged 60 years or olderNeurodegeneration and Stroke After Semaglutide and Tirzepatide in Patients With Diabetes and Obesity.
GLP-1RAs semaglutide and tirzepatideDecreases - greater benefitsrisk of dementia, stroke, and all-cause mortality
Human
womenNeurodegeneration and Stroke After Semaglutide and Tirzepatide in Patients With Diabetes and Obesity.
GLP-1RAs semaglutide and tirzepatideDecreases - greater benefitsrisk of dementia, stroke, and all-cause mortality
Human
patients with a body mass index of 30 to 40Neurodegeneration and Stroke After Semaglutide and Tirzepatide in Patients With Diabetes and Obesity.
semaglutideDecreases - reduced the risk ofall-cause mortality
Human
patients with HFpEF or HFmrEFComparative Effectiveness of Glucagon-like Peptide-1- Receptor Agonists in Patients With Heart Failure With Preserved or Minimally Reduced Ejection Fraction: A Comprehensive Bayesian Network Meta-Analysis and Network Meta-Regression.
semaglutideNo effect - did not affectcardiovascular mortality
Human
patients with HFpEF or HFmrEFComparative Effectiveness of Glucagon-like Peptide-1- Receptor Agonists in Patients With Heart Failure With Preserved or Minimally Reduced Ejection Fraction: A Comprehensive Bayesian Network Meta-Analysis and Network Meta-Regression.
semaglutideDecreases - conclusively shown to have cardioprotective effectscardiovascular mortality
Human
patients with diabetesNot specifiedEvidence-Based Cardiovascular Risk Management in Diabetes.cited 10×
semaglutideNo effect - absence of reductioncardiovascular mortality
Human
Cardiovascular outcome studies with incretin-based therapies: Comparison between DPP-4 inhibitors and GLP-1 receptor agonists.
semaglutideDecreases - showed more than 40% risk reductioncomposite of hospitalization for heart failure or all-cause mortality
Human
patients with cardiometabolic HFpEFSemaglutide and Tirzepatide in Patients With Heart Failure With Preserved Ejection Fraction.
once weekly semaglutideDecreases - decreased the incidencemajor adverse CV events and mortality
Human
Glucagon-like Peptide-1 Receptor Agonists and Cardiovascular Events: Class Effects versus Individual Patterns.
liraglutide and semaglutideDecreases - proved to be superiorCV morbidity and mortality
Human
patients with type 2 diabetesClinical implications of current cardiovascular outcome trials with sodium glucose cotransporter-2 (SGLT2) inhibitors.
Oral semaglutideDecreases - shows more significant advantages in reducingall-cause mortality
Human
patientsComparison of the efficacy and safety of GLP-1 receptor agonists on cardiovascular events and risk factors: A review and network meta-analysis.
Oral semaglutideDecreases - shows more significant advantages in reducingcardiovascular mortality
Human
patientsComparison of the efficacy and safety of GLP-1 receptor agonists on cardiovascular events and risk factors: A review and network meta-analysis.
semaglutide 2.4mg scDecreases - has shown a reductioncardiovascular mortality
Human
GLP-1 receptor agonists in obesity treatment: Effects on cardiometabolic variables and cardiovascular disease.
cagrilintide/semaglutide, liraglutide, semaglutide and tirzepatideNo effect - effectscardiovascular mortality
Human
patients with and without a history of HFCardiovascular 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.