Observational studyBMC nephrology2026
Patient characteristics and treatment efficacy after switching to hypoxia-inducible factor-prolyl hydroxylase inhibitors from erythropoiesis-stimulating agents in non-dialysis-dependent chronic kidney disease patients: the Reach-J CKD cohort study.
Observational study in BMC nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
15 authors.
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Abstract
backgroundHypoxia-inducible factor-prolyl hydroxylase inhibitors (HIF-PHIs) are likely to be effective in patients with anemia in chronic kidney disease (CKD) who are resistant to treatment with erythropoiesis-stimulating agents (ESAs). However, few studies assess HIF-PHIs in patients with elevated ERI who do not yet require hemodialysis.
methodsThis multicenter, prospective, observational study utilized data from the Reach-J study to explore the characteristics of Japanese patients with anemia in CKD (stage G3b-5) who switched from ESAs to HIF-PHIs. We also examined changes in hemoglobin levels following switching.
resultsWe assessed 447 patients who continued ESA treatment and 34 patients who switched from ESAs to HIF-PHIs (mean age: 74 years). Patients who switched had numerically higher mean erythropoietin resistance index (ERI) and numerically lower hemoglobin than those who continued ESA treatment. Mean hemoglobin levels increased following switching (9.9 g/dL vs. 10.6 g/dL; p = 0.004). After 3 months, hemoglobin levels increased in both high and low ERI subgroups (high ERI: 9.7 g/dL to 11.1 g/dL, low ERI: 10.6 g/dL to 11.8 g/dL). Hemoglobin levels did not notably decrease before or after the start of hemodialysis in two HIF-PHI-treated patients.
conclusionsPatients who switched to HIF-PHIs had low hemoglobin levels and high ERI compared with those who continued ESA treatment. Both high ERI and low ERI groups had increased hemoglobin levels after switching.
trial registrationUMIN Clinical Trials Registry (UMIN000022145, registration date: 30 April 2016).
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