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Published on: July 3, 2013
Kidney and heart failure outcomes associated with SGLT2 inhibitor use
Annemarie B van der Aart-van der Beek1,2, Rudolf A de Boer3, Hiddo J L Heerspink4,5
1Department of Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, Netherlands.
Insights
Sodium-glucose co-transporter 2 (SGLT2) inhibitors offer significant cardiovascular and kidney benefits for patients with chronic kidney disease (CKD) and heart failure. These agents are safe and effective across diverse patient groups, including those without diabetes.
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Chronic kidney disease (CKD) and heart failure are major global health concerns with high morbidity and mortality.
- Existing pharmacological treatments have limitations in improving outcomes for these conditions.
- Sodium-glucose co-transporter 2 (SGLT2) inhibitors, initially for type 2 diabetes, showed potential cardiovascular and renal benefits.
Purpose of the Study:
- To evaluate the cardiovascular and kidney protective effects of SGLT2 inhibitors in patients with CKD or heart failure.
- To assess the consistency of these benefits across various patient subgroups.
- To investigate the safety profile of SGLT2 inhibitors in these populations.
Main Methods:
- Clinical trials were conducted to assess SGLT2 inhibitors in patients with CKD and heart failure.
- Dedicated trials focused on cardiovascular and renal outcomes.
- Post-hoc analyses examined effects on specific complications like anemia and hyperkalemia, and safety parameters.
Main Results:
- SGLT2 inhibitors demonstrated consistent benefits in cardiovascular and renal outcomes across diverse patient subgroups, including those with and without type 2 diabetes, varying CKD stages, and different heart failure types.
- In patients with CKD, SGLT2 inhibitors were found to reduce the risk of anemia and hyperkalemia.
- Safety assessments indicated that SGLT2 inhibitors are generally well-tolerated, with no increased risk of hypoglycemia or acute kidney injury in the studied populations.
Conclusions:
- SGLT2 inhibitors represent a novel and effective treatment option for patients suffering from CKD and heart failure.
- Their benefits extend to patients irrespective of diabetes status, CKD stage, or heart failure classification.
- The favorable safety profile further supports their use in managing these complex conditions.
Abstract:
Chronic kidney disease (CKD) and heart failure affect many people worldwide. Despite the availability of pharmacological treatments, both diseases remain associated with considerable morbidity and mortality. After observations that sodium-glucose co-transporter 2 (SGLT2) inhibitors - originally developed as glucose-lowering agents - improved cardiovascular and renal outcomes in patients with type 2 diabetes, dedicated trials were initiated to evaluate the cardiovascular and kidney protective effects in patients with CKD or heart failure. The results of these clinical trials and subsequent detailed analyses have shown that the benefits of SGLT2 inhibitors are consistent across many patient subgroups, including those with and without type 2 diabetes, at different stages of CKD, and in patients with heart failure with preserved or reduced ejection fraction. In addition, post-hoc analyses revealed that SGLT2 inhibitors reduce the risk of anaemia and hyperkalaemia in patients with CKD. With respect to their safety, SGLT2 inhibitors are generally well tolerated. More specifically, no increased risk of hypoglycaemia has been observed in patients with CKD or heart failure without diabetes and they do not increase the risk of acute kidney injury. SGLT2 inhibitors therefore provide clinicians with an exciting new treatment option for patients with CKD and heart failure.
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