Abstract: SA-OR36
Effects of Dapagliflozin on Anemia in Patients With CKD With or Without Type 2 Diabetes: A Pre-Specified Analysis of the DAPA-CKD Trial
Session Information
- High-Impact CKD Potpourri: Something for Everyone
November 05, 2022 | Location: W307, Orange County Convention Center‚ West Building
Abstract Time: 05:15 PM - 05:24 PM
Category: Anemia and Iron Metabolism
- 200 Anemia and Iron Metabolism
Authors
- L Heerspink, Hiddo Jan, Universiteit Groningen Faculteit Medische Wetenschappen, Groningen, Groningen, Netherlands
- Koshino, Akihiko, Universiteit Groningen Faculteit Medische Wetenschappen, Groningen, Groningen, Netherlands
- Schechter, Meir, Universiteit Groningen Faculteit Medische Wetenschappen, Groningen, Groningen, Netherlands
- Vart, Priya, Universiteit Groningen Faculteit Medische Wetenschappen, Groningen, Groningen, Netherlands
- Jongs, Niels, Universiteit Groningen Faculteit Medische Wetenschappen, Groningen, Groningen, Netherlands
- Chertow, Glenn, Stanford Medicine, Stanford, California, United States
- Toto, Robert D., UT Southwestern Medical Center, Department of Internal Medicine, Dallas, Texas, United States
- Rossing, Peter, Steno Diabetes Center Copenhagen, Herlev, Denmark
- Correa-Rotter, Ricardo, National Medical Science and Nutrition Institute Salvador Zubiran, Mexico City, Mexico, Mexico
- McMurray, John, University of Glasgow Institute of Cardiovascular and Medical Sciences, Glasgow, Glasgow, United Kingdom
- Langkilde, Anna Maria, AstraZeneca, BioPharmaceuticals R&D, Gothenburg, Västergötland, Sweden
- Wheeler, David C., University College London Faculty of Medical Sciences, London, London, United Kingdom
Background
Anemia is a common complication of chronic kidney disease (CKD) and is associated with worse outcomes. The sodium-glucose cotransporter 2 inhibitor dapagliflozin increased erythropoietin and hematocrit (Hct) and corrected anemia in patients with heart failure. We examined the effect of dapagliflozin in preventing and correcting anemia in patients with CKD with or without type 2 diabetes (T2D).
Methods
The DAPA-CKD study randomized patients with eGFR 25-75 mL/min/1.73m2 and UACR 200-5000 mg/g to dapagliflozin 10mg or placebo. Hct was measured at baseline, 14 days, 2 and 4 months, and every 4 months thereafter. Anemia was defined as Hct levels <39% in males or <36% in females. Investigators’ reporting was used to define anemia-related adverse events. The effect of dapagliflozin on Hct was assessed using mixed effect model for repeated measures. Treatment effect in preventing and reversing anemia was assessed by Cox proportional hazard regression models.
Results
Of patients with Hct levels at baseline (N=4292 [99.7%]; mean Hct 38.9%), 1549 (36.1%) had anemia. Patients with anemia had lower mean eGFR (40 vs 45mL/min/1.73m2) and higher median UACR (1124 vs 877mg/g) compared to those without anemia. Over 2.4 years’ median follow-up, dapagliflozin increased absolute Hct levels vs placebo by 2.3% (95%CI 2.1-2.5; p<0.001). In patients without anemia at baseline, 134 (9.7%) developed anemia with dapagliflozin vs 228 (17.0%) with placebo (HR 0.53; 95%CI 0.43-0.66; p<0.001). Dapagliflozin reduced the risk of anemia-related adverse events compared to placebo (HR 0.46; 95%CI 0.23-0.95; p=0.04). In patients with anemia at baseline, anemia was corrected in 343 patients (47.5%) receiving dapagliflozin and 192 (24.8%) receiving placebo (HR 2.27; 95%CI 1.90-2.71; p<0.001). The effects of dapagliflozin in preventing and correcting anemia were consistent in patients with and without T2D (p interaction ≥0.83).
Conclusion
The effects of dapagliflozin on Hct may support its role in prevention and treatment of anemia in patients with CKD with or without T2D.
Funding
- Commercial Support – AstraZeneca