Dapagliflozin improves hemoglobin and anemia in chronic kidney disease: a systematic review and meta-analysis
Clinical Snapshot
PICO Framework
| P — Population | Patients with chronic kidney disease (CKD) and anemia |
| I — Intervention | Dapagliflozin (SGLT2 inhibitor) |
| C — Comparator | Control groups (placebo or standard care) |
| O — Outcomes | Hemoglobin levels, hematocrit, anemia outcomes, adverse events, mortality |
Bottom Line
This meta-analysis of eight studies suggests dapagliflozin may modestly improve hemoglobin levels in CKD patients by approximately 4.4 g/L. While statistically significant, the clinical significance is questionable given the small effect size and wide confidence intervals. The mechanism appears independent of glycemic control, potentially involving erythropoietin pathways. Safety profile was favourable with reduced overall adverse events and mortality. However, the evidence remains insufficient to recommend dapagliflozin specifically for CKD anemia management. The modest hemoglobin improvement may be a beneficial secondary effect in patients already prescribed SGLT2 inhibitors for established indications. Clinicians should await dedicated anemia-focused randomised trials before considering this as primary anemia therapy. Current evidence supports continuing established anemia treatments while recognising potential additive benefits in patients on dapagliflozin for other indications.
Key Findings
P Value: p = 0.02
Effect Size: Mean difference 4.37 g/L for hemoglobin
Primary Outcome: Hemoglobin increase of 4.37 g/L (95% CI: 0.71-8.03)
Nnt Or Sensitivity: Hematocrit sensitivity analysis: MD = 2.15% (95% CI: 1.86-2.44, p < 0.00001)
Confidence Interval: 95% CI: 0.71-8.03
Clinical Application
Dapagliflozin readily available but requires monitoring for ketoacidosis and volume depletion in CKD patients PBS-subsidised for diabetes and heart failure; TGA-approved but not specifically for CKD anemia; would require off-label use pending dedicated trials CKD patients with anemia, particularly those already on SGLT2 inhibitors for diabetes or cardiovascular protection
Abstract
Anemia becomes increasingly prevalent as kidney function declines. Current treatments carry multiple safety risks. Sodium-glucose cotransporter 2 inhibitors (SGLT2i), dapagliflozin, have emerged as background anemia modulator, a promising alternative, showing protective effects against anemia. This study synthesizes evidence on dapagliflozin's potential to improve anemia in chronic kidney disease (CKD) patients. A systematic review and meta-analysis was performed according to Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) guidelines, including eight studies identified from six databases. Risk of bias was assessed using tools appropriate for each study design (RoB 2, NOS, JBI). Data were pooled using a random-effects model with RevMan 5.4. The primary analysis for hemoglobin demonstrated significant increase (MD = 4.37; 95% CI = 0.71-8.03; p = 0.02) and remained significant in the sensitivity analysis (MD = 4.11; 95% CI = 0.19-8.04; p = 0.04). A sensitivity analysis for hematocrit revealed a highly significant increase (MD = 2.15; 95% CI = 1.86-2.44; p < 0.00001). In the sensitivity analysis for adverse events dapagliflozin significantly reduced the overall risk (RR = 0.77; 95% CI = 0.59-0.99; p = 0.04). This finding was associated with significantly lower mortality (RR = 0.67; p = 0.02), while no significant differences were observed for cardiovascular (p = 0.22) or genitourinary events (p = 0.70). Dapagliflozin is associated with clinically meaningful improvements in hemoglobin and anemia outcomes in CKD. These findings suggest a potential erythropoietic benefit beyond glycemic control, although dedicated anemia-focused trials are needed to confirm clinical applicability.
References
- 1.Irvania, Naufal, A., Tsauri, Ats, G. A., Yantisetiasti, Anglita, & Sofiatin, Y. (2026). Dapagliflozin improves hemoglobin and anemia in chronic kidney disease: a systematic review and meta-analysis. Renal Failure, 48(1). https://doi.org/10.1080/0886022X.2026.2636407
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