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First published online November 15, 2007
J Nucl Med 2007, doi:10.2967/jnumed.107.045427
© 2007 by Society of Nuclear Medicine
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Additive Effects of Spironolactone and Candesartan on Cardiac Sympathetic Nerve Activity and Left Ventricular Remodeling in Patients with Congestive Heart Failure

Shu Kasama 1*, Takuji Toyama 2, Hiroyuki Sumino 3, Naoya Matsumoto 4, Yuichi Sato 4, Hisao Kumakura 3, Yoshiaki Takayama 3, Shuichi Ichikawa 3, Tadashi Suzuki 2, and Masahiko Kurabayashi 2

1 Department of Cardiovascular Medicine, Gunma University School of Medicine, Maebashi, Japan; Department of Internal Medicine, Cardiovascular Hospital of Central Japan, Gunma, Japan
2 Department of Cardiovascular Medicine, Gunma University School of Medicine, Maebashi, Japan
3 Department of Internal Medicine, Cardiovascular Hospital of Central Japan, Gunma, Japan
4 Department of Cardiology, Nihon University School of Medicine, Tokyo, Japan

* To whom correspondence should be addressed. E-mail: s-kasama{at}bay.wind.ne.jp.


   Abstract

The activation of the renin–angiotensin–aldosterone system prevents the uptake of norepinephrine in the myocardium. However, the additive effects of combined spironolactone and candesartan on cardiac sympathetic nerve activity (CSNA) have not been determined. We investigated the effects of the angiotensin-receptor blocker candesartan alone and in combination with spironolactone on CSNA in patients with congestive heart failure (CHF). Methods: Fifty patients with CHF (left ventricular ejection fraction [LVEF] < 45%) were randomly assigned to candesartan plus spironolactone (group A; n = 25) or to candesartan alone (group B; n = 25). All patients were also treated with a loop diuretic. The delayed percent denervation, delayed heart-to-mediastinum count (H/M) ratio, and washout rate (WR) were determined from 123I-metaiodobenzylguanidine (MIBG) scintigraphy, and plasma brain natriuretic peptide (BNP) concentration was measured before and 6 mo after treatment. The LV end-diastolic volume (LVEDV), LV end-systolic volume (LVESV), and LVEF were also determined by echocardiography. Results: After 6 mo, all of these parameters were improved in both groups. However, the degree of change in the percent denervation was -14 ± 12 in group A and -7 ± 10 in group B (P < 0.05); the change in the H/M ratio was 0.19 ± 0.18 in group A and 0.08 ± 0.14 in group B (P < 0.05), the change in WR was -12% ± 8% in group A and -5% ± 13% in group B (P < 0.05), and the change in plasma BNP was -100 ± 83 pg/mL in group A and -43 ± 97 pg/mL in group B (P < 0.05). The degree of change in LVEDV, LVESV, and LVEF in group A tended to be better than that in group B, but these changes were not statistically significant. Moreover, there were significant correlations between changes in the 123I-MIBG scintigraphic findings and changes in the LVEDV (% denervation, r = 0.692, P < 0.001; H/M ratio, r = -0.437, P < 0.05; and WR, r = 0.505, P < 0.01) or the LVESV (% denervation, r = 0.663, P < 0.001; H/M ratio, r = -0.438, P < 0.05; and WR, r = 0.532, P < 0.01) in group A. In contrast, there was no relationship between these parameters in group B. Conclusion: These findings indicate that the combination of spironolactone and candesartan may be more beneficial for CSNA and LV performance than candesartan alone in patients with CHF.

Key Words: angiotensin, aldosterone, sympathetic nervous system




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