TY - JOUR
T1 - The predictability of renin–angiotensin–aldosterone system factors for clinical outcome in patients with acute decompensated heart failure
AU - Nakada, Yasuki
AU - Takahama, Hiroyuki
AU - Kanzaki, Hideaki
AU - Sugano, Yasuo
AU - Hasegawa, Takuya
AU - Ohara, Takahiro
AU - Amaki, Makoto
AU - Funada, Akira
AU - Yoshida, Akemi
AU - Yasuda, Satoshi
AU - Ogawa, Hisao
AU - Anzai, Toshihisa
N1 - Funding Information:
We thank Akiko Kada for her helpful advice regarding the statistical analyses. Funding Japan Cardiovascular Research Foundation (grant to H.T.)
Publisher Copyright:
© 2015, Springer Japan.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Although counter-regulation between B-type natriuretic peptide (BNP) levels and renin–angiotensin–aldosterone system (RAAS) activation in heart failure (HF) has been suggested, whether the regulation is preserved in acute decompensated heart failure (ADHF) patients remains unclear. This study aimed to determine: (1) the relationship between RAAS activation and clinical outcomes in ADHF patients, and (2) the relationships between plasma BNP levels and degrees of activation in RAAS factors. This study included ADHF patients (n = 103, NYHA3-4, plasma BNP > 200 pg/ml). We studied the predictability of RAAS factors for cardiovascular events and the relationships between plasma BNP levels and the degrees of activation in RAAS factors, which were evaluated by plasma renin activity (PRA) and aldosterone concentration (PAC). PRA was a strong predictor of cardiovascular (CV) events over 1 year, even after accounting for plasma BNP levels (hazard ratio (HR): 1.04, CI [1.02–1.06], p < 0.01) and medication such as RAAS blockers (HR: 1.03, CI [1.01–1.05], p < 0.01), whereas PAC was borderline-significant (univariate analysis, p = 0.06). Cut-off value of PRA (5.3 ng/ml/h) was determined by AUC curve. Of the enrolled patients, higher PRA was found in 40 % of them. Although no correlation between the plasma BNP levels and PRA was found (p = 0.36), after adjusting for hemodynamic parameters, eGFR and medication, a correlation was found between them (p = 0.01). Elevated RAAS factors were found in a substantial number of ADHF patients with high plasma BNP levels in the association with hemodynamic state, which predicts poor clinical outcomes. The measurements of RAAS factors help to stratify ADHF patients at risk for further CV events.
AB - Although counter-regulation between B-type natriuretic peptide (BNP) levels and renin–angiotensin–aldosterone system (RAAS) activation in heart failure (HF) has been suggested, whether the regulation is preserved in acute decompensated heart failure (ADHF) patients remains unclear. This study aimed to determine: (1) the relationship between RAAS activation and clinical outcomes in ADHF patients, and (2) the relationships between plasma BNP levels and degrees of activation in RAAS factors. This study included ADHF patients (n = 103, NYHA3-4, plasma BNP > 200 pg/ml). We studied the predictability of RAAS factors for cardiovascular events and the relationships between plasma BNP levels and the degrees of activation in RAAS factors, which were evaluated by plasma renin activity (PRA) and aldosterone concentration (PAC). PRA was a strong predictor of cardiovascular (CV) events over 1 year, even after accounting for plasma BNP levels (hazard ratio (HR): 1.04, CI [1.02–1.06], p < 0.01) and medication such as RAAS blockers (HR: 1.03, CI [1.01–1.05], p < 0.01), whereas PAC was borderline-significant (univariate analysis, p = 0.06). Cut-off value of PRA (5.3 ng/ml/h) was determined by AUC curve. Of the enrolled patients, higher PRA was found in 40 % of them. Although no correlation between the plasma BNP levels and PRA was found (p = 0.36), after adjusting for hemodynamic parameters, eGFR and medication, a correlation was found between them (p = 0.01). Elevated RAAS factors were found in a substantial number of ADHF patients with high plasma BNP levels in the association with hemodynamic state, which predicts poor clinical outcomes. The measurements of RAAS factors help to stratify ADHF patients at risk for further CV events.
KW - Acute decompensated heart failure
KW - BNP
KW - Renin–angiotensin–aldosterone system
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U2 - 10.1007/s00380-015-0688-7
DO - 10.1007/s00380-015-0688-7
M3 - Article
C2 - 25964073
AN - SCOPUS:84929179739
SN - 0910-8327
VL - 31
SP - 925
EP - 931
JO - Heart and Vessels
JF - Heart and Vessels
IS - 6
ER -