Dose Timing of an Angiotensin II Receptor Blocker/Calcium Channel Blocker Combination in Hypertensive Patients With Paroxysmal Atrial Fibrillation

Kazuomi Kario, Satoshi Hoshide, Kazuaki Uchiyama, Tetsuro Yoshida, Osamu Okazaki, Takao Noshiro, Hirotaka Aoki, Hiroyuki Mizuno, Yuri Matsumoto, Kazuomi Kario, Satoshi Hoshide, Kazuaki Uchiyama, Tetsuro Yoshida, Osamu Okazaki, Takao Noshiro, Hirotaka Aoki, Hiroyuki Mizuno, Yuri Matsumoto

Abstract

It has long been thought that there is a close association between hypertension and atrial fibrillation (AF). However, the efficacy of an angiotensin II receptor blocker for the prevention of organ damage in hypertensive individuals with AF is still controversial. The present study was a multicentered, prospective, randomized, open-label clinical trial investigating the differences in the effect of treatment with telmisartan/amlodipine combination tablets on blood pressure (BP) levels and BP variability between morning and bedtime administration in hypertensive patients with paroxysmal AF, using ambulatory BP monitoring (ABPM) and home BP. With this treatment, the patients' 24-hour BP, nighttime BP, preawake BP, and morning BP shown by ABPM were significantly reduced, and the antihypertensive effects were similar regardless of the timing of the drug administration. The standard deviation of day-by-day home systolic BP and the maximum home systolic BP were also significantly reduced, and these effects were similar regardless of the treatment timing. The N-terminal pro-brain natriuretic peptide level was significantly decreased only in the bedtime administration group. A larger study will demonstrate whether the bedtime administration of telmisartan/amlodipine combination tablets maximizes the risk-lowering effect against AF recurrence in paroxysmal AF hypertensive patients.

Trial registration: ClinicalTrials.gov NCT01748253.

©2016 Wiley Periodicals, Inc.

Figures

Figure 1
Figure 1
Study design. ABPM indicates ambulatory blood pressure monitoring; BP, blood pressure.
Figure 2
Figure 2
Patient disposition. One patient randomized to the morning group actually took the tablet at bedtime; two patients randomized to the bedtime group took the tablet in the morning. Therefore, the full analysis set consisted of 42 patients in the morning group and 39 patients in the bedtime group.

Source: PubMed

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