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Efficacy of angiotensin receptor neprilysin inhibitor in Asian patients with refractory hypertension
Sacubitril/valsartan, simultaneously inhibits neprilysin and angiotensin II receptor, showed an effect in reducing blood pressure (BP). The authors aimed to study whether it can be used as an antihypertensive agent in patients with refractory hypertension who have already been treated. A total of 66...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989761/ https://www.ncbi.nlm.nih.gov/pubmed/35253964 http://dx.doi.org/10.1111/jch.14454 |
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author | Li, Wanjing Gong, Minghui Yu, Qin Liu, Rihui Chen, Kaiming Lv, Wei Yao, Fumei Xu, Zhaolong Xu, Yi Song, Wei Jiang, Yinong |
author_facet | Li, Wanjing Gong, Minghui Yu, Qin Liu, Rihui Chen, Kaiming Lv, Wei Yao, Fumei Xu, Zhaolong Xu, Yi Song, Wei Jiang, Yinong |
author_sort | Li, Wanjing |
collection | PubMed |
description | Sacubitril/valsartan, simultaneously inhibits neprilysin and angiotensin II receptor, showed an effect in reducing blood pressure (BP). The authors aimed to study whether it can be used as an antihypertensive agent in patients with refractory hypertension who have already been treated. A total of 66 Chinese patients with refractory hypertension were enrolled. Patients received sacubitril/valsartan 200 instead of angiotensin II receptor blocker or angiotensin converting enzyme inhibitor while other agents continued. If BP was uncontrolled after 4 weeks, sacubitril/valsartan was increased to 400 mg. The BP reduction was evaluated by office BP and ambulatory BP monitoring after 8‐week treatment. The baseline office BP and mean arterial pressure (MAP) were 150.0/95.0 mmHg and 113.3 mmHg. BP and MAP reduced to 130.6/83.2 mmHg and 99.0 mmHg at week 8. Office BP and MAP reductions were 19.4/11.8 mmHg and 14.3 mmHg at endpoint (all p < .001). The 24‐h, daytime and nighttime ambulatory BP were 146.2/89.1, 148.1/90.3, and 137.5/83.7 mmHg, respectively at baseline, and BP reduced to 129.6/79.8, 130.6/81.1, and 121.7/75.8 mmHg, respectively at week 8. The 24‐h, daytime and nighttime ambulatory BP reductions were 16.6/9.3, 17.5/9.2, and 15.8/7.9 mmHg, respectively at endpoint (all p < .001). Sacubitril/valsartan significantly reduced office and ambulatory BP in refractory hypertension patients. Our study provided new evidence for sacubitril/valsartan in refractory hypertension. |
format | Online Article Text |
id | pubmed-8989761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89897612022-04-13 Efficacy of angiotensin receptor neprilysin inhibitor in Asian patients with refractory hypertension Li, Wanjing Gong, Minghui Yu, Qin Liu, Rihui Chen, Kaiming Lv, Wei Yao, Fumei Xu, Zhaolong Xu, Yi Song, Wei Jiang, Yinong J Clin Hypertens (Greenwich) Treatment Sacubitril/valsartan, simultaneously inhibits neprilysin and angiotensin II receptor, showed an effect in reducing blood pressure (BP). The authors aimed to study whether it can be used as an antihypertensive agent in patients with refractory hypertension who have already been treated. A total of 66 Chinese patients with refractory hypertension were enrolled. Patients received sacubitril/valsartan 200 instead of angiotensin II receptor blocker or angiotensin converting enzyme inhibitor while other agents continued. If BP was uncontrolled after 4 weeks, sacubitril/valsartan was increased to 400 mg. The BP reduction was evaluated by office BP and ambulatory BP monitoring after 8‐week treatment. The baseline office BP and mean arterial pressure (MAP) were 150.0/95.0 mmHg and 113.3 mmHg. BP and MAP reduced to 130.6/83.2 mmHg and 99.0 mmHg at week 8. Office BP and MAP reductions were 19.4/11.8 mmHg and 14.3 mmHg at endpoint (all p < .001). The 24‐h, daytime and nighttime ambulatory BP were 146.2/89.1, 148.1/90.3, and 137.5/83.7 mmHg, respectively at baseline, and BP reduced to 129.6/79.8, 130.6/81.1, and 121.7/75.8 mmHg, respectively at week 8. The 24‐h, daytime and nighttime ambulatory BP reductions were 16.6/9.3, 17.5/9.2, and 15.8/7.9 mmHg, respectively at endpoint (all p < .001). Sacubitril/valsartan significantly reduced office and ambulatory BP in refractory hypertension patients. Our study provided new evidence for sacubitril/valsartan in refractory hypertension. John Wiley and Sons Inc. 2022-03-07 /pmc/articles/PMC8989761/ /pubmed/35253964 http://dx.doi.org/10.1111/jch.14454 Text en © 2022 The Authors. The Journal of Clinical Hypertension published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Treatment Li, Wanjing Gong, Minghui Yu, Qin Liu, Rihui Chen, Kaiming Lv, Wei Yao, Fumei Xu, Zhaolong Xu, Yi Song, Wei Jiang, Yinong Efficacy of angiotensin receptor neprilysin inhibitor in Asian patients with refractory hypertension |
title | Efficacy of angiotensin receptor neprilysin inhibitor in Asian patients with refractory hypertension |
title_full | Efficacy of angiotensin receptor neprilysin inhibitor in Asian patients with refractory hypertension |
title_fullStr | Efficacy of angiotensin receptor neprilysin inhibitor in Asian patients with refractory hypertension |
title_full_unstemmed | Efficacy of angiotensin receptor neprilysin inhibitor in Asian patients with refractory hypertension |
title_short | Efficacy of angiotensin receptor neprilysin inhibitor in Asian patients with refractory hypertension |
title_sort | efficacy of angiotensin receptor neprilysin inhibitor in asian patients with refractory hypertension |
topic | Treatment |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989761/ https://www.ncbi.nlm.nih.gov/pubmed/35253964 http://dx.doi.org/10.1111/jch.14454 |
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