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Higher Hemoglobin Levels Using Darbepoetin Alfa and Kidney Outcomes in Advanced Chronic Kidney Disease Without Diabetes: a Prespecified Secondary Analysis of the PREDICT Trial

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Publisher Springer
Specialty Nephrology
Date 2023 Jun 8
PMID 37289335
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Abstract

Background: In the primary analysis of the PREDICT trial, a higher hemoglobin target (11-13 g/dl) with darbepoetin alfa did not improve renal outcomes compared with a lower hemoglobin target (9-11 g/dl) in advanced chronic kidney disease (CKD) without diabetes. Prespecified secondary analyses were performed to further study the effects of targeting higher hemoglobin levels on renal outcomes.

Methods: Patients with an estimated glomerular filtration rate (eGFR) 8-20 ml/min/1.73 m without diabetes were randomly assigned 1:1 to the high- and low-hemoglobin groups. The differences between the groups were evaluated for the following endpoints and cohort sets: eGFR and proteinuria slopes, assessed using a mixed-effects model in the full analysis set and the per-protocol set that excluded patients with off-target hemoglobin levels; the primary endpoint of composite renal outcome, evaluated in the per-protocol set using the Cox model.

Results: In the full analysis set (high hemoglobin, n = 239; low hemoglobin, n = 240), eGFR and proteinuria slopes were not significantly different between the groups. In the per-protocol set (high hemoglobin, n = 136; low hemoglobin, n = 171), the high-hemoglobin group was associated with reduced composite renal outcome (adjusted hazard ratio: 0.64; 95% confidence interval: 0.43-0.96) and an improved eGFR slope (coefficient: + 1.00 ml/min/1.73 m/year; 95% confidence interval: 0.38-1.63), while the proteinuria slope did not differ between the groups.

Conclusions: In the per-protocol set, the high-hemoglobin group demonstrated better kidney outcomes than the low-hemoglobin group, suggesting a potential benefit of maintaining higher hemoglobin levels in patients with advanced CKD without diabetes.

Clinical Trial Registration: Clinicaltrials.gov (identifier: NCT01581073).

References
1.
Iseki K, Iseki C, Ikemiya Y, Fukiyama K . Risk of developing end-stage renal disease in a cohort of mass screening. Kidney Int. 1996; 49(3):800-5. DOI: 10.1038/ki.1996.111. View

2.
Agodoa L, Appel L, Bakris G, Beck G, BOURGOIGNIE J, Briggs J . Effect of ramipril vs amlodipine on renal outcomes in hypertensive nephrosclerosis: a randomized controlled trial. JAMA. 2001; 285(21):2719-28. DOI: 10.1001/jama.285.21.2719. View

3.
Akizawa T, Macdougall I, Berns J, Bernhardt T, Staedtler G, Taguchi M . Long-Term Efficacy and Safety of Molidustat for Anemia in Chronic Kidney Disease: DIALOGUE Extension Studies. Am J Nephrol. 2019; 49(4):271-280. PMC: 6518868. DOI: 10.1159/000499111. View

4.
Macdougall I, Akizawa T, Berns J, Bernhardt T, Krueger T . Effects of Molidustat in the Treatment of Anemia in CKD. Clin J Am Soc Nephrol. 2018; 14(1):28-39. PMC: 6364546. DOI: 10.2215/CJN.02510218. View

5.
Xue J, St Peter W, Ebben J, Everson S, Collins A . Anemia treatment in the pre-ESRD period and associated mortality in elderly patients. Am J Kidney Dis. 2002; 40(6):1153-61. DOI: 10.1053/ajkd.2002.36861. View