Academic Journal

Canagliflozin and iron metabolism in the CREDENCE trial

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Canagliflozin and iron metabolism in the CREDENCE trial
Συγγραφείς: Koshino, A, Heerspink, HJL, Jongs, N, Badve, SV, Arnott, C, Neal, B, Jardine, M, Mahaffey, KW, Pollock, C, Perkovic, V, Hansen, MK, Bakker, SJL, Wada, T, Neuen, BL
Πηγή: urn:ISSN:0931-0509 ; urn:ISSN:1460-2385 ; Nephrology Dialysis Transplantation, 40, 4, 696-706
Στοιχεία εκδότη: Oxford University Press (OUP)
Έτος έκδοσης: 2025
Συλλογή: UNSW Sydney (The University of New South Wales): UNSWorks
Θεματικοί όροι: 32 Biomedical and Clinical Sciences, 3202 Clinical Sciences, Clinical Trials and Supportive Activities, Cardiovascular, Diabetes, Hematology, Clinical Research, Kidney Disease, Dietary Supplements, Nutrition, 6.1 Pharmaceuticals, 5.1 Pharmaceuticals, Renal and urogenital, 3 Good Health and Well Being, Humans, Male, Canagliflozin, Female, Middle Aged, Iron, Renal Insufficiency, Chronic, Aged, Sodium-Glucose Transporter 2 Inhibitors, Diabetes Mellitus, Type 2, Double-Blind Method, Follow-Up Studies, Prognosis, Glomerular Filtration Rate
Περιγραφή: Background. Studies in patients with heart failure have indicated that sodium-glucose cotransporter 2 (SGLT2) inhibitors increase iron use and enhance erythropoiesis. In this post hoc analysis of the Canagliflozin and Renal Endpoints in Diabetes with Established Nephropathy Clinical Evaluation (CREDENCE) trial, we evaluated the effects of canagliflozin on iron metabolism in patients with chronic kidney disease (CKD) and whether the effects of canagliflozin on hemoglobin and cardiorenal outcomes were modified by iron deficiency. Methods. We measured serum iron, total iron binding capacity (TIBC), transferrin saturation (TSAT) and ferritin at baseline and 12 months. The effects of canagliflozin, relative to placebo, on iron markers were assessed with analysis of covariance. Interactions between baseline iron deficiency, defined as TSAT <20%, and the effects of canagliflozin on hemoglobin and cardiorenal outcomes were evaluated with mixed effect models and Cox regression models, respectively. Results. Of 4401 participants randomized in CREDENCE, 2416 (54.9%) had iron markers measured at baseline, of whom 924 (38.2%) were iron deficient. Canagliflozin, compared with placebo, increased TIBC by 2.1% [95% confidence interval (CI) 0.4, 3.8; P = .014] and decreased ferritin by 11.5% (95% CI 7.1, 15.7; P < .001) with no clear effect on serum iron or TSAT. Canagliflozin increased hemoglobin over the trial duration by 7.3 g/L (95% CI 6.2, 8.5; P < .001) and 6.7 g/L (95% CI 5.2, 8.2; P < .001) in patients with and without iron deficiency, respectively (P for interaction = .38). The relative effect of canagliflozin on the primary outcome of doubling of serum creatinine, kidney failure or death due to cardiovascular disease or kidney failure (hazard ratio 0.70, 95% CI 0.56, 0.87) was consistent regardless of iron deficiency (P for interaction = .83), as were effects on other cardiovascular and mortality outcomes (all P for interactions ≥0.10). Conclusion. Iron deficiency is highly prevalent in patients with type 2 ...
Τύπος εγγράφου: article in journal/newspaper
Περιγραφή αρχείου: application/pdf
Γλώσσα: unknown
Relation: https://hdl.handle.net/1959.4/104434; https://doi.org/10.1093/ndt/gfae198
DOI: 10.1093/ndt/gfae198
Διαθεσιμότητα: https://hdl.handle.net/1959.4/104434
https://unsworks.unsw.edu.au/bitstreams/938a192a-8a6c-42ac-9bd6-9005506bb034/download
https://doi.org/10.1093/ndt/gfae198
Rights: open access ; https://purl.org/coar/access_right/c_abf2 ; CC BY ; https://creativecommons.org/licenses/by/4.0/ ; free_to_read
Αριθμός Καταχώρησης: edsbas.2618E8F2
Βάση Δεδομένων: BASE