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Cardiorenal protective effects of canagliflozin in CREDENCE according to glucose lowering

INTRODUCTION: Relationships between glycemic-lowering effects of sodium glucose co-transporter 2 inhibitors and impact on kidney and cardiovascular outcomes are uncertain. RESEARCH DESIGN AND METHODS: We analyzed 4395 individuals with prebaseline and postbaseline hemoglobin A1c (HbA1c) randomized to...

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Autores principales: Charytan, David M, Mahaffey, Kenneth W, Jardine, Meg J, Cannon, Christopher P, Neal, Bruce, Lambers Heerspink, Hiddo J, Agarwal, Rajiv, Bakris, George L, de Zeeuw, Dick, Levin, Adeera, Pollock, Carol, Zhang, Hong, Zinman, Bernard, Rosenthal, Norman, Perkovic, Vlado, Di Tanna, Gian Luca, Yu, Jie, Rogers, Kris, Arnott, Clare, Wheeler, David C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277062/
https://www.ncbi.nlm.nih.gov/pubmed/37311602
http://dx.doi.org/10.1136/bmjdrc-2022-003270
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author Charytan, David M
Mahaffey, Kenneth W
Jardine, Meg J
Cannon, Christopher P
Neal, Bruce
Lambers Heerspink, Hiddo J
Agarwal, Rajiv
Bakris, George L
de Zeeuw, Dick
Levin, Adeera
Pollock, Carol
Zhang, Hong
Zinman, Bernard
Rosenthal, Norman
Perkovic, Vlado
Di Tanna, Gian Luca
Yu, Jie
Rogers, Kris
Arnott, Clare
Wheeler, David C
author_facet Charytan, David M
Mahaffey, Kenneth W
Jardine, Meg J
Cannon, Christopher P
Neal, Bruce
Lambers Heerspink, Hiddo J
Agarwal, Rajiv
Bakris, George L
de Zeeuw, Dick
Levin, Adeera
Pollock, Carol
Zhang, Hong
Zinman, Bernard
Rosenthal, Norman
Perkovic, Vlado
Di Tanna, Gian Luca
Yu, Jie
Rogers, Kris
Arnott, Clare
Wheeler, David C
author_sort Charytan, David M
collection PubMed
description INTRODUCTION: Relationships between glycemic-lowering effects of sodium glucose co-transporter 2 inhibitors and impact on kidney and cardiovascular outcomes are uncertain. RESEARCH DESIGN AND METHODS: We analyzed 4395 individuals with prebaseline and postbaseline hemoglobin A1c (HbA1c) randomized to canagliflozin (n=2193) or placebo (n=2202) in The Canagliflozin and Renal Events in Diabetes with Established Nephropathy Clinical Evaluation trial. Effects on HbA1c were assessed using mixed models. Mediation of treatment effects by achieved glycemic control was analyzed using proportional hazards regression with and without adjustment for achieved HbA1c. End points included combined kidney or cardiovascular death, end-stage kidney disease or doubling of serum creatinine (primary trial outcome), and individual end point components. RESULTS: HbA1c lowering was modified by baseline estimated glomerular filtration rate (eGFR). For baseline eGFR 60–90, 45–59, and 30–44 mL/min/1.73 m(2), overall HbA1c (canagliflozin vs placebo) decreased by −0.24%, −0.14%, and −0.08% respectively and likelihood of >0.5% decrease in HbA1c decreased with ORs of 1.47 (95% CI 1.27 to 1.67), 1.12 (0.94 to 1.33) and 0.99 (0.83 to 1.18), respectively. Adjustment for postbaseline HbA1c marginally attenuated canagliflozin effects on primary and kidney composite outcomes: unadjusted HR 0.67 (95% CI 0.57 to 0.80) and 0.66 (95% CI 0.53 to 0.81); adjusted for week 13 HbA1c, HR 0.71 (95% CI 0.060 to 0.84) and 0.68 (95% CI 0.55 to 0.83). Results adjusted for time-varying HbA1c or HbA1c as a cubic spline were similar and consistent with preserved clinical benefits across a range of excellent and poor glycemic control. CONCLUSIONS: The glycemic effects of canagliflozin are attenuated at lower eGFR but effects on kidney and cardiac end points are preserved. Non-glycemic effects may be primarily responsible for the kidney and cardioprotective benefits of canagliflozin.22
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spelling pubmed-102770622023-06-19 Cardiorenal protective effects of canagliflozin in CREDENCE according to glucose lowering Charytan, David M Mahaffey, Kenneth W Jardine, Meg J Cannon, Christopher P Neal, Bruce Lambers Heerspink, Hiddo J Agarwal, Rajiv Bakris, George L de Zeeuw, Dick Levin, Adeera Pollock, Carol Zhang, Hong Zinman, Bernard Rosenthal, Norman Perkovic, Vlado Di Tanna, Gian Luca Yu, Jie Rogers, Kris Arnott, Clare Wheeler, David C BMJ Open Diabetes Res Care Cardiovascular and Metabolic Risk INTRODUCTION: Relationships between glycemic-lowering effects of sodium glucose co-transporter 2 inhibitors and impact on kidney and cardiovascular outcomes are uncertain. RESEARCH DESIGN AND METHODS: We analyzed 4395 individuals with prebaseline and postbaseline hemoglobin A1c (HbA1c) randomized to canagliflozin (n=2193) or placebo (n=2202) in The Canagliflozin and Renal Events in Diabetes with Established Nephropathy Clinical Evaluation trial. Effects on HbA1c were assessed using mixed models. Mediation of treatment effects by achieved glycemic control was analyzed using proportional hazards regression with and without adjustment for achieved HbA1c. End points included combined kidney or cardiovascular death, end-stage kidney disease or doubling of serum creatinine (primary trial outcome), and individual end point components. RESULTS: HbA1c lowering was modified by baseline estimated glomerular filtration rate (eGFR). For baseline eGFR 60–90, 45–59, and 30–44 mL/min/1.73 m(2), overall HbA1c (canagliflozin vs placebo) decreased by −0.24%, −0.14%, and −0.08% respectively and likelihood of >0.5% decrease in HbA1c decreased with ORs of 1.47 (95% CI 1.27 to 1.67), 1.12 (0.94 to 1.33) and 0.99 (0.83 to 1.18), respectively. Adjustment for postbaseline HbA1c marginally attenuated canagliflozin effects on primary and kidney composite outcomes: unadjusted HR 0.67 (95% CI 0.57 to 0.80) and 0.66 (95% CI 0.53 to 0.81); adjusted for week 13 HbA1c, HR 0.71 (95% CI 0.060 to 0.84) and 0.68 (95% CI 0.55 to 0.83). Results adjusted for time-varying HbA1c or HbA1c as a cubic spline were similar and consistent with preserved clinical benefits across a range of excellent and poor glycemic control. CONCLUSIONS: The glycemic effects of canagliflozin are attenuated at lower eGFR but effects on kidney and cardiac end points are preserved. Non-glycemic effects may be primarily responsible for the kidney and cardioprotective benefits of canagliflozin.22 BMJ Publishing Group 2023-06-13 /pmc/articles/PMC10277062/ /pubmed/37311602 http://dx.doi.org/10.1136/bmjdrc-2022-003270 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Cardiovascular and Metabolic Risk
Charytan, David M
Mahaffey, Kenneth W
Jardine, Meg J
Cannon, Christopher P
Neal, Bruce
Lambers Heerspink, Hiddo J
Agarwal, Rajiv
Bakris, George L
de Zeeuw, Dick
Levin, Adeera
Pollock, Carol
Zhang, Hong
Zinman, Bernard
Rosenthal, Norman
Perkovic, Vlado
Di Tanna, Gian Luca
Yu, Jie
Rogers, Kris
Arnott, Clare
Wheeler, David C
Cardiorenal protective effects of canagliflozin in CREDENCE according to glucose lowering
title Cardiorenal protective effects of canagliflozin in CREDENCE according to glucose lowering
title_full Cardiorenal protective effects of canagliflozin in CREDENCE according to glucose lowering
title_fullStr Cardiorenal protective effects of canagliflozin in CREDENCE according to glucose lowering
title_full_unstemmed Cardiorenal protective effects of canagliflozin in CREDENCE according to glucose lowering
title_short Cardiorenal protective effects of canagliflozin in CREDENCE according to glucose lowering
title_sort cardiorenal protective effects of canagliflozin in credence according to glucose lowering
topic Cardiovascular and Metabolic Risk
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277062/
https://www.ncbi.nlm.nih.gov/pubmed/37311602
http://dx.doi.org/10.1136/bmjdrc-2022-003270
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