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Efficacy and Safety of Esaxerenone in Hypertensive Patients with Diabetic Kidney Disease: A Multicenter, Open-Label, Prospective Study

INTRODUCTION: Clinical data of esaxerenone in hypertensive patients with diabetic kidney disease (DKD) are lacking. We evaluated the efficacy and safety of esaxerenone in patients with DKD and an inadequate response to blood pressure (BP)-lowering treatment. METHODS: In this multicenter, open-label,...

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Autores principales: Uchida, Haruhito A., Nakajima, Hirofumi, Hashimoto, Masami, Nakamura, Akihiko, Nunoue, Tomokazu, Murakami, Kazuharu, Hosoya, Takeshi, Komoto, Kiichi, Taguchi, Takashi, Akasaka, Takaaki, Shiosakai, Kazuhito, Sugimoto, Kotaro, Wada, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449923/
https://www.ncbi.nlm.nih.gov/pubmed/36070133
http://dx.doi.org/10.1007/s12325-022-02294-z
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author Uchida, Haruhito A.
Nakajima, Hirofumi
Hashimoto, Masami
Nakamura, Akihiko
Nunoue, Tomokazu
Murakami, Kazuharu
Hosoya, Takeshi
Komoto, Kiichi
Taguchi, Takashi
Akasaka, Takaaki
Shiosakai, Kazuhito
Sugimoto, Kotaro
Wada, Jun
author_facet Uchida, Haruhito A.
Nakajima, Hirofumi
Hashimoto, Masami
Nakamura, Akihiko
Nunoue, Tomokazu
Murakami, Kazuharu
Hosoya, Takeshi
Komoto, Kiichi
Taguchi, Takashi
Akasaka, Takaaki
Shiosakai, Kazuhito
Sugimoto, Kotaro
Wada, Jun
author_sort Uchida, Haruhito A.
collection PubMed
description INTRODUCTION: Clinical data of esaxerenone in hypertensive patients with diabetic kidney disease (DKD) are lacking. We evaluated the efficacy and safety of esaxerenone in patients with DKD and an inadequate response to blood pressure (BP)-lowering treatment. METHODS: In this multicenter, open-label, prospective study, patients were divided into urinary albumin-to-creatinine ratio subcohorts (UACR < 30, 30 to < 300, and 300 to < 1000 mg/gCr). Esaxerenone was initiated at 1.25 mg/day and followed by incremental dose escalation based on BP and serum potassium level monitoring. The treatment period was 12 weeks. The primary endpoint was change in morning home systolic BP/diastolic BP (SBP/DBP) from baseline to end of treatment (EOT). Secondary endpoints included achievement rate of target BP, change in UACR from baseline, and safety. RESULTS: In total, 113 patients were enrolled. Morning home SBP/DBP significantly decreased from baseline to EOT in the total population (− 11.6/− 5.2 mmHg, both p < 0.001) and in all UACR subcohorts (all p < 0.001). The target BP achievement rate was 38.5%. Significant reductions in bedtime home and office BPs were also shown in the total population and all UACR subcohorts. UACR significantly improved from baseline to EOT in the total (− 50.9%, p < 0.001) and all UACR subcohorts (all p < 0.001). Incidence of serum potassium elevation as drug-related treatment emergent adverse events was 2.7%. The change from baseline in estimated glomerular filtration rate (eGFR) was − 4.8 mL/min/1.73 m(2). CONCLUSION: Esaxerenone demonstrated a BP-lowering effect and improved albuminuria. The effects were consistent regardless of the severity of albuminuria without clinically relevant serum potassium elevation and eGFR reduction. CLINICAL TRIAL REGISTRATION: jRCTs06119002. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12325-022-02294-z.
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spelling pubmed-94499232022-09-07 Efficacy and Safety of Esaxerenone in Hypertensive Patients with Diabetic Kidney Disease: A Multicenter, Open-Label, Prospective Study Uchida, Haruhito A. Nakajima, Hirofumi Hashimoto, Masami Nakamura, Akihiko Nunoue, Tomokazu Murakami, Kazuharu Hosoya, Takeshi Komoto, Kiichi Taguchi, Takashi Akasaka, Takaaki Shiosakai, Kazuhito Sugimoto, Kotaro Wada, Jun Adv Ther Original Research INTRODUCTION: Clinical data of esaxerenone in hypertensive patients with diabetic kidney disease (DKD) are lacking. We evaluated the efficacy and safety of esaxerenone in patients with DKD and an inadequate response to blood pressure (BP)-lowering treatment. METHODS: In this multicenter, open-label, prospective study, patients were divided into urinary albumin-to-creatinine ratio subcohorts (UACR < 30, 30 to < 300, and 300 to < 1000 mg/gCr). Esaxerenone was initiated at 1.25 mg/day and followed by incremental dose escalation based on BP and serum potassium level monitoring. The treatment period was 12 weeks. The primary endpoint was change in morning home systolic BP/diastolic BP (SBP/DBP) from baseline to end of treatment (EOT). Secondary endpoints included achievement rate of target BP, change in UACR from baseline, and safety. RESULTS: In total, 113 patients were enrolled. Morning home SBP/DBP significantly decreased from baseline to EOT in the total population (− 11.6/− 5.2 mmHg, both p < 0.001) and in all UACR subcohorts (all p < 0.001). The target BP achievement rate was 38.5%. Significant reductions in bedtime home and office BPs were also shown in the total population and all UACR subcohorts. UACR significantly improved from baseline to EOT in the total (− 50.9%, p < 0.001) and all UACR subcohorts (all p < 0.001). Incidence of serum potassium elevation as drug-related treatment emergent adverse events was 2.7%. The change from baseline in estimated glomerular filtration rate (eGFR) was − 4.8 mL/min/1.73 m(2). CONCLUSION: Esaxerenone demonstrated a BP-lowering effect and improved albuminuria. The effects were consistent regardless of the severity of albuminuria without clinically relevant serum potassium elevation and eGFR reduction. CLINICAL TRIAL REGISTRATION: jRCTs06119002. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12325-022-02294-z. Springer Healthcare 2022-09-07 2022 /pmc/articles/PMC9449923/ /pubmed/36070133 http://dx.doi.org/10.1007/s12325-022-02294-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Uchida, Haruhito A.
Nakajima, Hirofumi
Hashimoto, Masami
Nakamura, Akihiko
Nunoue, Tomokazu
Murakami, Kazuharu
Hosoya, Takeshi
Komoto, Kiichi
Taguchi, Takashi
Akasaka, Takaaki
Shiosakai, Kazuhito
Sugimoto, Kotaro
Wada, Jun
Efficacy and Safety of Esaxerenone in Hypertensive Patients with Diabetic Kidney Disease: A Multicenter, Open-Label, Prospective Study
title Efficacy and Safety of Esaxerenone in Hypertensive Patients with Diabetic Kidney Disease: A Multicenter, Open-Label, Prospective Study
title_full Efficacy and Safety of Esaxerenone in Hypertensive Patients with Diabetic Kidney Disease: A Multicenter, Open-Label, Prospective Study
title_fullStr Efficacy and Safety of Esaxerenone in Hypertensive Patients with Diabetic Kidney Disease: A Multicenter, Open-Label, Prospective Study
title_full_unstemmed Efficacy and Safety of Esaxerenone in Hypertensive Patients with Diabetic Kidney Disease: A Multicenter, Open-Label, Prospective Study
title_short Efficacy and Safety of Esaxerenone in Hypertensive Patients with Diabetic Kidney Disease: A Multicenter, Open-Label, Prospective Study
title_sort efficacy and safety of esaxerenone in hypertensive patients with diabetic kidney disease: a multicenter, open-label, prospective study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449923/
https://www.ncbi.nlm.nih.gov/pubmed/36070133
http://dx.doi.org/10.1007/s12325-022-02294-z
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