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Updated: Jul 28, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Dapagliflozin in people with chronic kidney disease
Rochelle D Sylvester1, Teck K Khong2
1Clinical Pharmacology, St George's University of London, London, UK.
Insights
Dapagliflozin significantly slowed chronic kidney disease progression in patients with and without diabetes. This sodium-glucose cotransporter-2 inhibitor demonstrated substantial renal benefits, offering a new treatment avenue.
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Chronic kidney disease (CKD) affects millions globally, leading to kidney failure.
- Current treatments for CKD primarily manage symptoms and slow progression.
- There is a need for therapies that target underlying disease mechanisms to preserve kidney function.
Purpose of the Study:
- To evaluate the efficacy of dapagliflozin in slowing the progression of CKD.
- To assess the impact of dapagliflozin on kidney and cardiovascular outcomes in patients with CKD.
Main Methods:
- A large-scale, randomized, placebo-controlled trial involving patients with CKD.
- Participants received dapagliflozin or a placebo, with outcomes monitored over time.
- Key endpoints included a composite of kidney function decline and cardiovascular events.
Main Results:
- Dapagliflozin significantly reduced the risk of CKD progression by 30% compared to placebo.
- The drug demonstrated a 30% reduction in the risk of cardiovascular death or heart failure hospitalization.
- Adverse events were generally similar between the dapagliflozin and placebo groups.
Conclusions:
- Dapagliflozin is effective in slowing the progression of chronic kidney disease.
- The sodium-glucose cotransporter-2 inhibitor offers significant cardiorenal protection.
- Dapagliflozin represents a major advancement in CKD management for a broad patient population.
Abstract:
Commentary on: Heerspink HJL, Stefánsson BV, Correa-Rotter R, et al Dapagliflozin in patients with chronic kidney disease. N Engl J Med 2020;383:1436-46. Series Editor: Dr Teck Khong, DTB Associate Editor, Clinical Pharmacology, St George's, University of London, UK.
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