BLOOD PRESSURE LOWERING EFFICACY OF SACUBITRIL/ALLISARTAN VERSUS OLMESARTAN IN CHINESE HYPERTENSIVE PATIENTS WITH A NON-DIPPING BLOOD PRESSURE PATTERN

Objective: Abnormal nocturnal blood pressure dipping profile is an important cardiovascular risk factor in patients with hypertension. This analysis aimed to investigate the effects of Sacubitril/Allisartan on blood pressure in Chinese patients with mild to moderate hypertension and a nighttime non-dipping pattern. Design and method: We performed analysis of data from a randomized clinical trial that compared the blood pressure-lowering effect at 12 weeks of treatment with Sacubitril/Allisartan (240 or 480 mg/d) and Olmesartan (20 mg/d). Nighttime non-dipping pattern was defined as mean nighttime (10 pm-6 am) ambulatory blood pressure fall of <10% versus daytime (6 am-10 pm) ambulatory blood pressure. The outcome measures included clinical and 24-hour, daytime, and nighttime ambulatory blood pressure. Results: Of the 1197 randomized patients of the trial, 497 (41.5%) patients had a nighttime non-dipping pattern and were included in this analysis. The least square mean (±standard error) changes from baseline in 24 h mean ambulatory systolic/diastolic blood pressure (maSBP/maDBP) in the Sacubitril/Allisartan 240 and 480 mg/day groups were -10.3 ± 1.1/-5.3 ± 0.6 and -13.7 ± 1.1/-6.7 ± 0.6 mmHg, respectively. The reductions in nighttime maSBP were significantly greater with both doses of Sacubitril/Allisartan compared with Olmesartan 20 mg (-12.7±1.2/6.3±0.7 mmHg, with a difference of -3.8 [-7.2 to -0.4] mmHg, P=0.029 for Sacubitril/Allisartan 240 mg and -7.5 [-10.9 to -4.1] mmHg, P<0.001 for Sacubitril/Allisartan 480 mg). The 24-h mean ambulatory blood pressure and nighttime maSBP reductions in non-dipper patients tended to be dose-dependent for Sacubitril/Allisartan. At 12 weeks of treatment, the prevalence of dippers was higher in the Sacubitril/Allisartan 240 and 480 mg groups than in the Olmesartan 20 mg group for both systolic (46.9% and 47.9% vs 33.7%) and diastolic blood pressure (42.0% and 40.2% vs 26.5%), being statistically significant for the 480 mg group (P=0.011, 0.008, and 0.002 respectively). Conclusions: Sacubitril/Allisartan is particularly effective in reducing nighttime blood pressure and in reversing the non-dipping to dipping nighttime blood pressure pattern.

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Journal
Journal of Hypertension
Published
2025-05-01
DOI
https://doi.org/10.1097/01.hjh.0001117384.06706.dd
Primary Topic
Blood Pressure and Hypertension Studies
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article
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article

BLOOD PRESSURE LOWERING EFFICACY OF SACUBITRIL/ALLISARTAN VERSUS OLMESARTAN IN CHINESE HYPERTENSIVE PATIENTS WITH A NON-DIPPING BLOOD PRESSURE PATTERN

Shao-Xing Chen, Jin Zhang, Ji‐Guang Wang, Zichen Liu et al.
Journal of Hypertension
Blood Pressure and Hypertension Studies
article

BLOOD PRESSURE LOWERING EFFICACY OF SACUBITRIL/ALLISARTAN VERSUS OLMESARTAN IN CHINESE HYPERTENSIVE PATIENTS WITH A NON-DIPPING BLOOD PRESSURE PATTERN

Shao-Xing Chen, Jin Zhang, Ji‐Guang Wang, Zichen Liu, Jinfeng Li, Yan Li, Qiang Wang, Jingchao Sun, Wenjie Xu, Qian Ge, Xiangnan Zhou, Xiaohong Lu, Jie Yan, Wei Zhang
article en

Abstract

Objective: Abnormal nocturnal blood pressure dipping profile is an important cardiovascular risk factor in patients with hypertension. This analysis aimed to investigate the effects of Sacubitril/Allisartan on blood pressure in Chinese patients with mild to moderate hypertension and a nighttime non-dipping pattern. Design and method: We performed analysis of data from a randomized clinical trial that compared the blood pressure-lowering effect at 12 weeks of treatment with Sacubitril/Allisartan (240 or 480 mg/d) and Olmesartan (20 mg/d). Nighttime non-dipping pattern was defined as mean nighttime (10 pm-6 am) ambulatory blood pressure fall of <10% versus daytime (6 am-10 pm) ambulatory blood pressure. The outcome measures included clinical and 24-hour, daytime, and nighttime ambulatory blood pressure. Results: Of the 1197 randomized patients of the trial, 497 (41.5%) patients had a nighttime non-dipping pattern and were included in this analysis. The least square mean (±standard error) changes from baseline in 24 h mean ambulatory systolic/diastolic blood pressure (maSBP/maDBP) in the Sacubitril/Allisartan 240 and 480 mg/day groups were -10.3 ± 1.1/-5.3 ± 0.6 and -13.7 ± 1.1/-6.7 ± 0.6 mmHg, respectively. The reductions in nighttime maSBP were significantly greater with both doses of Sacubitril/Allisartan compared with Olmesartan 20 mg (-12.7±1.2/6.3±0.7 mmHg, with a difference of -3.8 [-7.2 to -0.4] mmHg, P=0.029 for Sacubitril/Allisartan 240 mg and -7.5 [-10.9 to -4.1] mmHg, P<0.001 for Sacubitril/Allisartan 480 mg). The 24-h mean ambulatory blood pressure and nighttime maSBP reductions in non-dipper patients tended to be dose-dependent for Sacubitril/Allisartan. At 12 weeks of treatment, the prevalence of dippers was higher in the Sacubitril/Allisartan 240 and 480 mg groups than in the Olmesartan 20 mg group for both systolic (46.9% and 47.9% vs 33.7%) and diastolic blood pressure (42.0% and 40.2% vs 26.5%), being statistically significant for the 480 mg group (P=0.011, 0.008, and 0.002 respectively). Conclusions: Sacubitril/Allisartan is particularly effective in reducing nighttime blood pressure and in reversing the non-dipping to dipping nighttime blood pressure pattern.

Journal of HypertensionVol. 43(Suppl 1)
Shanghai Jiao Tong University (CN), Ruijin Hospital (CN), Shanghai Institute of Hypertension (CN), State Key Laboratory of Medical Genomics
Zero hunger
Openalex Percentile: Top 80%
Blood Pressure and Hypertension Studies
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