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- PMID: 33747548
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Article: Cardiovascular Outcomes in Trials of New Antidiabetic Drug Classes
Title | Cardiovascular Outcomes in Trials of New Antidiabetic Drug Classes |
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Authors | |
Keywords | Antidiabetic drug sodium–glucose co-transporter 2 inhibitor glucagon-like peptide 1 receptor agonist dipeptidyl peptidase-4 inhibitor type 2 diabetes |
Issue Date | 2021 |
Publisher | Radcliffe Cardiology. The Journal's web site is located at https://www.cfrjournal.com/ |
Citation | Cardiac Failure Review, 2021, v. 7, p. article no. e04 How to Cite? |
Abstract | Type 2 diabetes is among the most prevalent chronic diseases worldwide and the prevention of associated cardiovascular complications is an important treatment goal. Sodium–glucose co-transporter 2 (SGLT2) inhibitors, glucagon-like peptide 1 (GLP-1) receptor agonists and dipeptidyl peptidase-4 (DPP-4) inhibitors are second-line options after metformin, while cardiovascular outcome trials have been conducted to establish the cardiovascular safety of these antidiabetic drug classes. SGLT2 inhibitors have been shown to have the best overall mortality, renal and cardiovascular outcomes. Reduction in hospitalisation for heart failure is particularly consistent. GLP-1 receptor agonists have also showed some benefits, especially in stroke prevention. DPP-4 inhibitors showed neutral effects on cardiovascular outcomes, but may increase the incidence of heart failure. Favourable outcomes observed in trials of SGLT2 inhibitors mean that these should be the preferred second-line option. DPP-4 inhibitors are useful for patients with diabetes at low cardiovascular risk. |
Persistent Identifier | http://hdl.handle.net/10722/304691 |
ISSN | 2023 Impact Factor: 4.2 2023 SCImago Journal Rankings: 0.975 |
PubMed Central ID |
DC Field | Value | Language |
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dc.contributor.author | Lo, CWH | - |
dc.contributor.author | Fei, Y | - |
dc.contributor.author | Cheung, BMY | - |
dc.date.accessioned | 2021-10-05T02:33:46Z | - |
dc.date.available | 2021-10-05T02:33:46Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Cardiac Failure Review, 2021, v. 7, p. article no. e04 | - |
dc.identifier.issn | 2057-7540 | - |
dc.identifier.uri | http://hdl.handle.net/10722/304691 | - |
dc.description.abstract | Type 2 diabetes is among the most prevalent chronic diseases worldwide and the prevention of associated cardiovascular complications is an important treatment goal. Sodium–glucose co-transporter 2 (SGLT2) inhibitors, glucagon-like peptide 1 (GLP-1) receptor agonists and dipeptidyl peptidase-4 (DPP-4) inhibitors are second-line options after metformin, while cardiovascular outcome trials have been conducted to establish the cardiovascular safety of these antidiabetic drug classes. SGLT2 inhibitors have been shown to have the best overall mortality, renal and cardiovascular outcomes. Reduction in hospitalisation for heart failure is particularly consistent. GLP-1 receptor agonists have also showed some benefits, especially in stroke prevention. DPP-4 inhibitors showed neutral effects on cardiovascular outcomes, but may increase the incidence of heart failure. Favourable outcomes observed in trials of SGLT2 inhibitors mean that these should be the preferred second-line option. DPP-4 inhibitors are useful for patients with diabetes at low cardiovascular risk. | - |
dc.language | eng | - |
dc.publisher | Radcliffe Cardiology. The Journal's web site is located at https://www.cfrjournal.com/ | - |
dc.relation.ispartof | Cardiac Failure Review | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Antidiabetic drug | - |
dc.subject | sodium–glucose co-transporter 2 inhibitor | - |
dc.subject | glucagon-like peptide 1 receptor agonist | - |
dc.subject | dipeptidyl peptidase-4 inhibitor | - |
dc.subject | type 2 diabetes | - |
dc.title | Cardiovascular Outcomes in Trials of New Antidiabetic Drug Classes | - |
dc.type | Article | - |
dc.identifier.email | Cheung, BMY: mycheung@hkucc.hku.hk | - |
dc.identifier.authority | Cheung, BMY=rp01321 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.15420/cfr.2020.19 | - |
dc.identifier.pmid | 33747548 | - |
dc.identifier.pmcid | PMC7970669 | - |
dc.identifier.hkuros | 326196 | - |
dc.identifier.volume | 7 | - |
dc.identifier.spage | article no. e04 | - |
dc.identifier.epage | article no. e04 | - |
dc.publisher.place | United Kingdom | - |