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Effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease

Alacepril is a relatively novel angiotensin-converting enzyme inhibitor; however, the safety, tolerance, and efficacy of alacepril in terms of cough suppression in dogs with mitral valve disease (MVD) remain unknown. The aim of this study was to investigate the safety, tolerance, and cough suppressi...

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Autores principales: HORI, Yasutomo, NAKAMURA, Kensuke, KANNO, Nobuyuki, HITOMI, Makoto, YAMASHITA, Yohei, HOSAKA, Satoshi, ISAYAMA, Noriko, MIMURA, Takahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115264/
https://www.ncbi.nlm.nih.gov/pubmed/29937457
http://dx.doi.org/10.1292/jvms.17-0557
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author HORI, Yasutomo
NAKAMURA, Kensuke
KANNO, Nobuyuki
HITOMI, Makoto
YAMASHITA, Yohei
HOSAKA, Satoshi
ISAYAMA, Noriko
MIMURA, Takahiro
author_facet HORI, Yasutomo
NAKAMURA, Kensuke
KANNO, Nobuyuki
HITOMI, Makoto
YAMASHITA, Yohei
HOSAKA, Satoshi
ISAYAMA, Noriko
MIMURA, Takahiro
author_sort HORI, Yasutomo
collection PubMed
description Alacepril is a relatively novel angiotensin-converting enzyme inhibitor; however, the safety, tolerance, and efficacy of alacepril in terms of cough suppression in dogs with mitral valve disease (MVD) remain unknown. The aim of this study was to investigate the safety, tolerance, and cough suppression efficacy of alacepril in dogs with MVD. This was a multi-center, prospective study. Forty-two dogs with echocardiographic or radiographic evidence of cardiac enlargement in addition to cough were enrolled. Dogs were treated with alacepril (1.0–3.0 mg/kg/day) for at least 4 weeks. One dog (2.4%) developed complications, including appetite loss, lethargy, and vomiting. Thirty-six dogs were re-evaluated after 4 weeks of treatment. Cough resolved or improved in 20 dogs (55.6%) after treatment. Based on the efficacy of alacepril, the dogs were divided into an effective group (n=20) and an ineffective group (n=16). After treatment, the left ventricular end-diastolic internal diameter corrected for body weight was significantly increased from baseline in the ineffective group but was significantly decreased in the effective group. Univariate binomial logistic regression analyses showed that high atrial natriuretic peptide level, N-terminal pro-B-type natriuretic peptide level, and E wave velocity at baseline were significantly correlated with alacepril inefficacy. Alacepril as treatment for MVD is well tolerated in most dogs, and different conditions of cardiac loading may influence the effect of the drug. Alacepril is expected to improve the quality of life of dogs with early stage MVD.
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spelling pubmed-61152642018-09-24 Effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease HORI, Yasutomo NAKAMURA, Kensuke KANNO, Nobuyuki HITOMI, Makoto YAMASHITA, Yohei HOSAKA, Satoshi ISAYAMA, Noriko MIMURA, Takahiro J Vet Med Sci Internal Medicine Alacepril is a relatively novel angiotensin-converting enzyme inhibitor; however, the safety, tolerance, and efficacy of alacepril in terms of cough suppression in dogs with mitral valve disease (MVD) remain unknown. The aim of this study was to investigate the safety, tolerance, and cough suppression efficacy of alacepril in dogs with MVD. This was a multi-center, prospective study. Forty-two dogs with echocardiographic or radiographic evidence of cardiac enlargement in addition to cough were enrolled. Dogs were treated with alacepril (1.0–3.0 mg/kg/day) for at least 4 weeks. One dog (2.4%) developed complications, including appetite loss, lethargy, and vomiting. Thirty-six dogs were re-evaluated after 4 weeks of treatment. Cough resolved or improved in 20 dogs (55.6%) after treatment. Based on the efficacy of alacepril, the dogs were divided into an effective group (n=20) and an ineffective group (n=16). After treatment, the left ventricular end-diastolic internal diameter corrected for body weight was significantly increased from baseline in the ineffective group but was significantly decreased in the effective group. Univariate binomial logistic regression analyses showed that high atrial natriuretic peptide level, N-terminal pro-B-type natriuretic peptide level, and E wave velocity at baseline were significantly correlated with alacepril inefficacy. Alacepril as treatment for MVD is well tolerated in most dogs, and different conditions of cardiac loading may influence the effect of the drug. Alacepril is expected to improve the quality of life of dogs with early stage MVD. The Japanese Society of Veterinary Science 2018-06-22 2018-08 /pmc/articles/PMC6115264/ /pubmed/29937457 http://dx.doi.org/10.1292/jvms.17-0557 Text en ©2018 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Internal Medicine
HORI, Yasutomo
NAKAMURA, Kensuke
KANNO, Nobuyuki
HITOMI, Makoto
YAMASHITA, Yohei
HOSAKA, Satoshi
ISAYAMA, Noriko
MIMURA, Takahiro
Effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease
title Effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease
title_full Effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease
title_fullStr Effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease
title_full_unstemmed Effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease
title_short Effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease
title_sort effects of the angiotensin-converting enzyme inhibitor alacepril in dogs with mitral valve disease
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115264/
https://www.ncbi.nlm.nih.gov/pubmed/29937457
http://dx.doi.org/10.1292/jvms.17-0557
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