Comparison of blood pressure variability between losartan and amlodipine in essential hypertension (COMPAS-BPV)

Jun Won Lee, Eunhee Choi, Jung Woo Son, Young Jin Youn, Sung Gyun Ahn, Min Soo Ahn, Jang Young Kim, Seung Hwan Lee, Junghan Yoon, Dong Ryeol Ryu, Sang Min Park, Kyung Soon Hong, Byung Su Yoo

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

BACKGROUND: Antihypertensive therapy using renin-angiotensin system blockers and calcium channel blockers to target blood pressure variability (BPV) has not yet been established. We aimed to compare the ability of losartan and amlodipine to lower BPV and systolic blood pressure (SBP) in essential hypertensive patients. METHODS: Patients were randomly assigned either losartan 50 mg or amlodipine 5 mg. Medications were uptitrated and hydrochlorothiazide was added according to protocol for 6 months. The primary endpoint was the office visit-to-visit SD of SBP. The secondary endpoints included average real variability (ARV), office SBP, and home SBP. RESULTS: The losartan group (n = 71) and amlodipine group (n = 73) finished the scheduled visits between April 2013 and May 2017. The office visit-to-visit SD of SBP was comparable between the losartan and amlodipine groups (11.0 ± 4.2 vs. 10.5 ± 3.8, P = 0.468). The office visit-to-visit ARV of SBP was significantly elevated in the losartan group (10.6 ± 4.3 vs. 9.1 ± 3.4, P = 0.02). The absolute SBP decrement from baseline to 6 months was similar between groups, although the office mean SBP at 6 months was higher in the losartan group (132.3 ± 12.9 vs. 127.5 ± 9.0 mm Hg, P = 0.011). In home blood pressure analysis, evening day-to-day BPV indexes (SD and ARV) were significantly higher in the losartan group at 6 months. CONCLUSIONS: The lowering effect of the office visit-to-visit SD of SBP was similar between losartan and amlodipine. However, the losartan group showed a higher office visit-to-visit ARV of SBP and evening day-to-day home BPV indexes. Therefore, amlodipine may be better to lower BPV in essential hypertensive patients.

Original languageEnglish
Pages (from-to)748-755
Number of pages8
JournalAmerican journal of hypertension
Volume33
Issue number8
DOIs
Publication statusPublished - 2020 Aug 1

Bibliographical note

Funding Information:
This study was supported by Pfizer Inc., New York, NY (WS2124990). As this is an investigator-initiated trial, the authors designed and conducted the study. The funding body does not interfere with the analysis and interpretation of the data.

Publisher Copyright:
© American Journal of Hypertension, Ltd 2020. All rights reserved.

All Science Journal Classification (ASJC) codes

  • Internal Medicine

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