Abstract: PO2364
DAPA-CKD: A Regional Analysis of Kidney and Cardiovascular Outcomes
Session Information
- CKD: Insights from Recent Clinical Trials and Large Real-World Effectiveness Studies
 November 04, 2021 | Location: On-Demand, Virtual Only
 Abstract Time: 10:00 AM - 12:00 PM
Category: CKD (Non-Dialysis)
- 2102 CKD (Non-Dialysis): Clinical, Outcomes, and Trials
Authors
- Correa-Rotter, Ricardo, The National Medical Science and Nutrition Institute Salvador Zubiran, Mexico City, Mexico
- Vart, Priya, University Medical Center Groningen, Groningen, Netherlands
- Jongs, Niels, University Medical Center Groningen, Groningen, Netherlands
- Hou, Fan Fan, Southern Medical University, National Clinical Research Center for Kidney Disease, Guangzhou, China
- Chertow, Glenn Matthew, Stanford University School of Medicine, Stanford, California, United States
- Langkilde, Anna Maria, AstraZeneca, Gothenburg, Sweden
- McMurray, John, University of Glasgow, Glasgow, Glasgow, United Kingdom
- Rossing, Peter, Steno Diabetes Center Copenhagen, Gentofte, Denmark
- Sjostrom, David, AstraZeneca, Gothenburg, Sweden
- Stefansson, Bergur V., AstraZeneca, Gothenburg, Sweden
- Toto, Robert D., UT Southwestern Medical Center, Dallas, Texas, United States
- Douthat, Walter, Hospital Privado Universitario de Cordoba, Cordoba, Argentina
- Escudero, Elizabeth Teresa, Hospital Arzobispo Loayza, Cayetano Heredia University, Lima, Peru
- Isidto, Rey A., Healthlink Medical, Dental, Surgical Clinics and Diagnostics Center, Iloilo City, Philippines
- Khullar, Dinesh, Max Super Speciality Hospital Saket, New Delhi, Delhi, India
- Bajaj, Harpreet S., LMC Diabetes and Endocrinology, Brampton, Ontario, Canada
- Wheeler, David C., University College London, London, London, United Kingdom
- L Heerspink, Hiddo Jan, University Medical Center Groningen, Groningen, Netherlands
Background
The DAPA-CKD trial (NCT03036150) demonstrated that dapagliflozin reduced the risk of kidney and cardiovascular (CV) events in patients with chronic kidney disease (CKD) and albuminuria, with and without type 2 diabetes. We aimed to determine whether the effects of dapagliflozin varied by pre-specified geographic region.
Methods
We randomized 4304 adults with baseline estimated glomerular filtration rate (eGFR) 25–75 mL/min/1.73m2 and urinary albumin-to-creatinine ratio 200–5000 mg/g to dapagliflozin 10mg or placebo once daily; median follow-up was 2.4 years. We compared baseline data, primary and secondary outcomes, and safety of the 4 regions (Asia, Northern America, Latin America, Europe).
Results
Compared to other regions, participants from Asia had lower body mass index, less frequent use of diuretics and better blood pressure control. The figure displays the primary and secondary outcomes by region and treatment assignment. Dapagliflozin consistently reduced the risk of the primary composite endpoint (eGFR decline ≥50%, end-stage kidney disease, or kidney or CV death) across the 4 regions by 30 to 49%, with no significant heterogeneity (p=0.77). Similarly, there was no evidence of differences in secondary outcomes between regions. Serious adverse events in the dapagliflozin and placebo groups were similar across the 4 regions.
Conclusion
Despite differences in patient characteristics, the beneficial effects of dapagliflozin on kidney and CV endpoints in patients with CKD and albuminuria were similar across pre-specified geographic regions.
Funding
- Commercial Support – AstraZeneca
 
                                            