TY - JOUR
T1 - Influence of left ventricular ejection fraction on the effects of supplemental use of angiotensin receptor blocker olmesartan in hypertensive patients with heart failure
AU - SUPPORT Trial Investigators
AU - Miura, Masanobu
AU - Sakata, Yasuhiko
AU - Miyata, Satoshi
AU - Shiba, Nobuyuki
AU - Takahashi, Jun
AU - Nochioka, Kotaro
AU - Takada, Tsuyoshi
AU - Saga, Chiharu
AU - Shinozaki, Tsuyoshi
AU - Sugi, Masafumi
AU - Nakagawa, Makoto
AU - Sekiguchi, Nobuyo
AU - Komaru, Tatsuya
AU - Kato, Atsushi
AU - Fukuchi, Mitsumasa
AU - Nozaki, Eiji
AU - Hiramoto, Tetsuya
AU - Inoue, Kanichi
AU - Goto, Toshikazu
AU - Ohe, Masatoshi
AU - Tamaki, Kenji
AU - Ibayashi, Setsuro
AU - Ishide, Nobumasa
AU - Maruyama, Yukio
AU - Tsuji, Ichiro
AU - Shimokawa, Hiroaki
N1 - Publisher Copyright:
© 2016, Japanese Circulation Society. All rights reserved.
PY - 2016
Y1 - 2016
N2 - Background: There is no robust evidence of pharmacological interventions to improve mortality in heart failure (HF) patients with preserved left ventricular ejection fraction (LVEF) (HFpEF). In this subanalysis study of the SUPPORT Trial, we addressed the influence of LVEF on the effects of olmesartan in HF. Methods and Results: Among 1,147 patients enrolled in the SUPPORT Trial, we examined 429 patients with reduced LVEF (HFrEF, LVEF <50%) and 709 with HFpEF (LVEF ≥50%). During a median follow-up of 4.4 years, 21.9% and 12.5% patients died in the HFrEF and HFpEF groups, respectively. In HFrEF patients, the addition of olmesartan to the combination of angiotensin-converting enzyme inhibitor (ACEI) and β-blocker (BB) was associated with increased incidence of death (hazard ratio (HR) 2.26, P=0.002) and worsening renal function (HR 2.01, P=0.01), whereas its addition to ACEI or BB alone was not. In contrast, in HFpEF patients, the addition of olmesartan to BB alone was significantly associated with reduced mortality (HR 0.32, P=0.03), whereas with ACEIs alone or in combination with BB and ACEI was not. The linear mixed-effect model showed that in HFpEF, the urinary albumin/ creatinine ratio was unaltered when BB were combined with olmesartan, but significantly increased when not combined with olmesartan (P=0.01). Conclusions: LVEF substantially influences the effects of additive use of olmesartan, with beneficial effects noted when combined with BB in hypertensive HFpEF patients.
AB - Background: There is no robust evidence of pharmacological interventions to improve mortality in heart failure (HF) patients with preserved left ventricular ejection fraction (LVEF) (HFpEF). In this subanalysis study of the SUPPORT Trial, we addressed the influence of LVEF on the effects of olmesartan in HF. Methods and Results: Among 1,147 patients enrolled in the SUPPORT Trial, we examined 429 patients with reduced LVEF (HFrEF, LVEF <50%) and 709 with HFpEF (LVEF ≥50%). During a median follow-up of 4.4 years, 21.9% and 12.5% patients died in the HFrEF and HFpEF groups, respectively. In HFrEF patients, the addition of olmesartan to the combination of angiotensin-converting enzyme inhibitor (ACEI) and β-blocker (BB) was associated with increased incidence of death (hazard ratio (HR) 2.26, P=0.002) and worsening renal function (HR 2.01, P=0.01), whereas its addition to ACEI or BB alone was not. In contrast, in HFpEF patients, the addition of olmesartan to BB alone was significantly associated with reduced mortality (HR 0.32, P=0.03), whereas with ACEIs alone or in combination with BB and ACEI was not. The linear mixed-effect model showed that in HFpEF, the urinary albumin/ creatinine ratio was unaltered when BB were combined with olmesartan, but significantly increased when not combined with olmesartan (P=0.01). Conclusions: LVEF substantially influences the effects of additive use of olmesartan, with beneficial effects noted when combined with BB in hypertensive HFpEF patients.
KW - Angiotensin II receptor blocker
KW - Heart failure with preserved ejection fraction
KW - Hypertension
KW - Olmesartan
KW - Prognosis
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U2 - 10.1253/circj.CJ-16-0577
DO - 10.1253/circj.CJ-16-0577
M3 - Article
C2 - 27628221
AN - SCOPUS:84988664223
SN - 1346-9843
VL - 80
SP - 2155
EP - 2164
JO - Circulation Journal
JF - Circulation Journal
IS - 10
ER -