The Place and Value of Sodium-Glucose Cotransporter 2 Inhibitors in the Evolving Treatment Paradigm for Type 2 Diabetes Mellitus: A Narrative Review.

Cardiorenal protection Cardiovascular disease Cardiovascular risk Chronic kidney disease Diabetic kidney disease Heart failure Oral glucose-lowering medicines Prescribing tools SGLT2 inhibitors Type 2 diabetes mellitus

Journal

Diabetes therapy : research, treatment and education of diabetes and related disorders
ISSN: 1869-6953
Titre abrégé: Diabetes Ther
Pays: United States
ID NLM: 101539025

Informations de publication

Date de publication:
May 2022
Historique:
received: 20 12 2021
accepted: 08 02 2022
pubmed: 22 3 2022
medline: 22 3 2022
entrez: 21 3 2022
Statut: ppublish

Résumé

Over recent years, the expanding evidence base for sodium-glucose cotransporter-2 inhibitor (SGLT2i) therapies has revealed benefits beyond their glucose-lowering efficacy in the treatment of Type 2 diabetes mellitus (T2DM), resulting in their recognition as cardiorenal medicines. While SGLT2is continue to be recommended among the second-line therapies for the treatment of hyperglycaemia, their true value now extends to the prevention of debilitating and costly cardiovascular and renal events for high-risk individuals, with particular benefit shown in reducing major adverse cardiac events and heart failure (HF) and slowing the progression of chronic kidney disease. However, SGLT2i usage is still suboptimal among groups considered to be at greatest risk of cardiorenal complications. The ongoing coronavirus disease 2019 (COVID-19) pandemic has intensified financial pressures on healthcare systems, which may hamper further investment in newer effective medicines. Emerging evidence indicates that glycaemic control should be prioritised for people with T2DM in the era of COVID-19 and practical advice on the use of T2DM medications during periods of acute illness remains important, particularly for healthcare professionals working in primary care who face multiple competing priorities. This article provides the latest update from the Improving Diabetes Steering Committee, including perspectives on the value of SGLT2is as cost-effective therapies within the T2DM treatment paradigm, with particular focus on the latest published evidence relating to the prevention or slowing of cardiorenal complications. The implications for ongoing and future approaches to diabetes care are considered in the light of the continuing coronavirus pandemic, and relevant aspects of international treatment guidelines are highlighted with practical advice on the appropriate use of SGLT2is in commonly occurring T2DM clinical scenarios. The 'SGLT2i Prescribing Tool for T2DM Management', previously published by the Steering Committee, has been updated to reflect the latest evidence and is provided in the Supplementary Materials to help support clinicians delivering T2DM care.

Identifiants

pubmed: 35307801
doi: 10.1007/s13300-022-01228-w
pii: 10.1007/s13300-022-01228-w
pmc: PMC8934539
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

847-872

Informations de copyright

© 2022. The Author(s).

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Auteurs

John P H Wilding (JPH)

Department of Cardiovascular and Metabolic Medicine, Institute of Life Course and Medical Sciences, Clinical Sciences Centre, University Hospital Aintree, Liverpool, UK. j.p.h.wilding@liverpool.ac.uk.

Marc Evans (M)

University Hospital Llandough, Cardiff, UK.

Kevin Fernando (K)

North Berwick Health Centre, North Berwick, UK.

Jose Luis Gorriz (JL)

University Hospital Clinic, University of Valencia, Valencia, Spain.

Ana Cebrian (A)

Spanish Diabetes Association, Catholic University of Murcia, Service Murciano de Salud, Cartagena, Murcia, Spain.
Centro de Salud Casco Antiguo Cartagena, Murcia, Spain.
Primary Care Research Group, Biomedical Research Institute of Murcia (IMIB), 30120, Murcia, Spain.

Jane Diggle (J)

College Lane Surgery, Ackworth, West Yorkshire, UK.

Debbie Hicks (D)

TREND Diabetes, Enfield, UK.

June James (J)

University Hospitals of Leicester NHS Trust, Leicester, UK.

Philip Newland-Jones (P)

University Hospitals Southampton NHS Foundation Trust, Southampton, UK.

Amar Ali (A)

Royal Blackburn Hospital, Lancashire, UK.

Stephen Bain (S)

Swansea University and Diabetes Research Unit, Swansea, UK.

Andrea Da Porto (A)

University of Udine, Udine, Italy.

Dipesh Patel (D)

University College London, London, UK.

Adie Viljoen (A)

Cambridge University Hospitals NHS Foundation Trust, Stevenage, UK.

David C Wheeler (DC)

University College London, London, UK.

Stefano Del Prato (S)

University of Pisa, Pisa, Italy.

Classifications MeSH