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SGLT2 Inhibitors: Cardiovascular Benefits Beyond HbA1c-Translating Evidence into Practice
Amar Ali1, Steve Bain2, Debbie Hicks3
1Oakenhurst Medical Practice, Blackburn, UK.
Insights
Sodium-glucose co-transporter-2 inhibitors (SGLT2i) reduce cardiovascular disease (CVD) risk in type 2 diabetes mellitus (T2DM). This guidance helps healthcare professionals use SGLT2i therapies to maximize benefits for T2DM patients with CVD risk.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Cardiovascular disease (CVD), including heart failure (HF), is a major cause of death in type 2 diabetes mellitus (T2DM).
- Shared risk factors and overlapping outcomes link CVD and T2DM.
- Sodium-glucose co-transporter-2 inhibitors (SGLT2i) show proven cardiovascular (CV) benefits in T2DM patients.
Purpose of the Study:
- To provide practical, evidence-based guidance on using SGLT2i therapies in T2DM management.
- To stratify guidance by CVD risk in T2DM patients.
- To support healthcare professionals in selecting appropriate SGLT2i therapies.
Main Methods:
- Review of recent cardiovascular outcomes trials (CVOTs) and real-world studies.
- Building upon previous consensus documents on SGLT2i use in T2DM.
- Focus on maximizing pleiotropic benefits of SGLT2i for CVD risk reduction.
Main Results:
- SGLT2i therapies demonstrate robust evidence in reducing adverse CV outcomes for T2DM patients.
- Guidance addresses the need for updated treatment recommendations reflecting new evidence.
- Practical advice is offered for optimizing SGLT2i use in T2DM with varying CVD risk.
Conclusions:
- SGLT2i are valuable in managing T2DM, particularly for reducing CVD risk.
- Updated guidance is crucial as some clinical guidelines lag behind current evidence.
- This paper empowers HCPs to effectively utilize SGLT2i for CVD prevention in T2DM.
Abstract:
Cardiovascular disease (CVD), including heart failure (HF), is a leading cause of morbidity and mortality in people with type 2 diabetes mellitus (T2DM). CVD and T2DM share common risk factors for development and progression, and there is significant overlap between the conditions in terms of worsening outcomes. In assessing the cardiovascular (CV) safety profiles of anti-diabetic drugs, sodium-glucose co-transporter-2 inhibitor (SGLT2i) therapies have emerged with robust evidence for reducing the risk of adverse CVD outcomes in people with T2DM who have either established CVD or are at risk of developing CVD. A previous consensus document from the Improving Diabetes Steering Committee has examined the potential role of SGLT2is in T2DM management and considered the risk-benefit profile of the class and the appropriate place for these medicines within the T2DM pathway. This paper builds on these findings and presents practical guidance for maximising the pleiotropic benefits of this class of medicines in people with T2DM in terms of reducing adverse CVD outcomes. The Improving Diabetes Steering Committee aims to offer evidence-based practical guidance for the use of SGLT2i therapies in people with T2DM stratified by CVD risk. This is of particular importance currently because some treatment guidelines have not been updated to reflect recent evidence from cardiovascular outcomes trials (CVOTs) and real-world studies that complement the CVOTs. The Improving Diabetes Steering Committee seeks to support healthcare professionals (HCPs) in appropriate treatment selection for people with T2DM who are at risk of developing or have established CVD and examines the role of SGLT2i therapy for these people.Funding: Napp Pharmaceuticals Limited.
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