Cardiovascular protection with sodium-glucose co-transporter-2 inhibitors in type 2 diabetes: Does it apply to all patients?


Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
09 2020
Historique:
received: 02 12 2019
revised: 04 04 2020
accepted: 05 04 2020
pubmed: 15 4 2020
medline: 25 6 2021
entrez: 15 4 2020
Statut: ppublish

Résumé

Patients with type 2 diabetes (T2D) are at an increased risk of cardiovascular disease (CVD). Cardiovascular risk in these patients should be considered as a continuum, and comprehensive treatment strategies should aim to target multiple disease risk factors. Large-scale clinical trials of sodium-glucose co-transporter-2 (SGLT2) inhibitors have shown an impact on cardiovascular outcomes, including heart failure hospitalization and cardiovascular death, which appears to be independent of their glucose-lowering efficacy. Reductions in major cardiovascular events appear to be greatest in patients with established CVD, particularly those with prior myocardial infarction, but are independent of heart failure or renal risk. Most large-scale trials of SGLT2 inhibitors predominantly include patients with T2D with pre-existing CVD and high cardiovascular risk at baseline, limiting their applicability to patients typically observed in clinical practice. Real-world evidence from observational studies suggests that there might also be beneficial effects of SGLT2 inhibitors on heart failure hospitalization and all-cause mortality in various cohorts of lower risk patients. The most common adverse events reported in clinical and observational studies are genital infections; however, the overall risk of these events appears to be low and easily managed. Similar safety profiles have been reported for elderly and younger patients. There is still some debate regarding the safety of canagliflozin in patients at high risk of fracture and amputation. Outstanding questions include specific patterns of cardiovascular protection according to baseline risk.

Identifiants

pubmed: 32285611
doi: 10.1111/dom.14055
pmc: PMC7496739
doi:

Substances chimiques

Sodium-Glucose Transporter 2 Inhibitors 0
Symporters 0
Sodium 9NEZ333N27
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1481-1495

Subventions

Organisme : AstraZeneca
Pays : International

Informations de copyright

© 2020 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

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Auteurs

Francesco Giorgino (F)

Department of Emergency and Organ Transplantation, University of Bari Aldo Moro, Bari, Italy.

Jiten Vora (J)

Department of Diabetes and Endocrinology, University of Liverpool, Liverpool, UK.

Peter Fenici (P)

AstraZeneca, Cambridge, UK.

Anna Solini (A)

Department of Surgical, Medical, Molecular and Critical Area Pathology, University of Pisa, Pisa, Italy.

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