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SAVOR-TIMI to DECLARE-TIMI: A Review on Cardiovascular Outcome Trials of Incretin-modulators and Gliflozins.

Indian J Endocrinol Metab · 2019

Last updated 2026-05-28

Since 2008, studies have tested diabetes drugs for their effects on heart health in people with type 2 diabetes and high heart disease risk. Some drugs, like saxagliptin, were neutral for heart outcomes but increased hospital stays for heart failure. Others, like empagliflozin and canagliflozin, reduced major heart events and heart failure hospitalizations. Among GLP-1 drugs, liraglutide, semaglutide, and albiglutide lowered major heart events, with liraglutide also reducing heart-related and overall deaths.

AI summary of the abstract below.

JournalIndian J Endocrinol Metab, 2019
Citations2
Relative citation ratio0.08
NIH percentile6
Molecules
Conditions studied Type 2 Diabetes, Cardiovascular Risk Reduction

Abstract

INTRODUCTION: Since 2008 United State (US) food drug administration mandate, several newer anti-diabetic drugs (ADD) have undergone a mandatory cardiovascular (CV) outcome trial (CVOT) in type diabetes (T2DM) patients with high CV risk. These includes CVOT done with dipeptidyl-peptidase-4 inhibitors, sodium-glucose co-transporter-2 inhibitors and glucagon-like peptide-1 receptor agonist (GLP-1RAs). Several double-blind, randomized, placebo-controlled CVOT have been presented and published in the last decade (2008-2018). AIMS AND OBJECTIVES: We systematically searched the database of PubMed and ClinicalTrials.gov from January 1, 2008 to December 31, 2018 using specific key words. Subsequently, we pooled the data of different cardiovascular endpoints and made a comparative forest plot using GraphPad software Inc. Prism Version 8, US. RESULTS AND CONCLUSION: Saxagliptin, alogliptin, sitagliptin and linagliptin are CV neutral drugs. Saxagliptin showed a significantly higher hospitalization due to heart failure (HHF). Empagliflozin and canagliflozin have shown a significant reduction in composite of 3-point major cardiac adverse events (3P-MACE). Additionally, empagliflozin, canagliflozin and dapagliflozin significantly reduced the HHF and the composite of CV death or HHF. Moreover, empagliflozin showed significant reduction in CV- and all-cause death in patients with T2DM with established CV disease. While both exendin-backbone-based GLP-1RAs such as lixisenatide and extended-release exenatide were CV neutral; GLP-1-backbone-based GLP-1RAs such as liraglutide, semaglutide and albiglutide shown a significant reduction in the composite of 3-P MACE. Additionally, liraglutide shown a significant reduction in CV- and all-cause death. Moreover, semaglutide reduced non-fatal stroke and albiglutide reduced myocardial infarction, while extended-release exenatide reduced all-cause death; however, value of significance for these outcomes should be considered nominal.

Verbatim abstract via PubMed 31161099 ↗