Dose-Dependent Prognostic Effect of Carvedilol in Patients With Chronic Heart Failure::Special Reference to Ranscardiac Gradient of Norepinephrine

K. Nishiyama, T. Tsutamoto, Masayuki Yamaji, Chiho Kawahara, Takashi Yamamoto, M. Fujii, M. Horie
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引用次数: 2

Abstract

he β-blockers improve cardiac function and prolong survival in patients with systolic chronic heart failure (CHF).1–4 In the Multicenter Oral Carvedilol Heart Failure Assessment (MOCHA) trial, carvedilol (6.25– 25 mg/day) was associated with dose-related improvements in left ventricular (LV) function and survival in heart failure (HF) patients in a population that was 77% Caucasian.5 However, the response to carvedilol may vary among different ethnic groups6–9 and indeed, the dose of carvedilol for treatment in Japanese is 10–20 mg/day, which is less than half of the dose used in Western patients.10,11 In the Multicenter Carvedilol Heart Failure Dose Assessment (MUCHA) trial, low-dose carvedilol (5 mg/day group or 20 mg/day group) improved the LV ejection fraction (LVEF) and reduced cardiovascular hospitalization in Japanese patients with CHF.12 In addition, carvedilol therapy achieved a dose-related improvement in CHF and LVEF; cardiovascular hospitalization was markedly reduced. However, the relationship between the dose-dependent improvement of carvedilol and prognosis in Japanese patients with CHF remains unknown. Cardiac sympathetic nerve activity (CSA) plays an important role in the pathophysiology of CHF.13–17 We previously reported that CSA plays an important role in the pathophysiology of CHF, independent of hemodynamic overload, and that the transcardiac gradient of norepinephrine (NE) is a more reliable biomarker of CSA than the peripheral venous NE level.18,19 Moreover, carvedilol treatment has been reported as associated with a significant reduction in the transcardiac gradient of NE, without any changes in the plasma arterial NE, in patients with CHF.20 There has not previously been a study correlating the transcardiac gradient of NE, brain natriuretic peptide (BNP) and N-terminal BNP (NT-proBNP) with the dose of carvedilol. In the present study, we investigated the relationship of these parameters with the prognosis of CHF in the same population.
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卡维地洛对慢性心力衰竭患者的剂量依赖性预后影响:特别参考去甲肾上腺素的心肌梯度
β受体阻滞剂可改善收缩期慢性心力衰竭(CHF)患者的心功能并延长生存期。1-4在多中心口服卡维地洛心力衰竭评估(MOCHA)试验中,卡维地洛(6.25 - 25mg /天)与心力衰竭(HF)患者左心室(LV)功能和生存率的剂量相关改善相关,该试验中白人占77%。5然而,不同种族对卡维地洛的反应可能不同6 - 9,事实上,卡维地洛在日本的治疗剂量为10 - 20mg /天,不到西方患者使用剂量的一半。10,11在多中心卡维地洛心力衰竭剂量评估(MUCHA)试验中,低剂量卡维地洛(5mg /天组或20mg /天组)改善了日本CHF患者的左室射血分数(LVEF)并降低了心血管住院率。12此外,卡维地洛治疗实现了CHF和LVEF的剂量相关改善;心血管住院治疗明显减少。然而,卡维地洛剂量依赖性改善与日本CHF患者预后之间的关系尚不清楚。心脏交感神经活动(CSA)在CHF的病理生理中起重要作用。13 - 17我们之前报道过CSA在CHF的病理生理中起重要作用,独立于血流动力学超载,并且去甲肾上腺素(NE)的经心梯度是CSA比外周静脉NE水平更可靠的生物标志物。18,19此外,据报道,卡维地洛治疗可显著降低chf患者的NE经心梯度,而血浆动脉NE无任何变化。20此前没有研究将NE、脑利钠肽(BNP)和n端BNP (NT-proBNP)的经心梯度与卡维地洛的剂量联系起来。在本研究中,我们研究了这些参数与同一人群中CHF预后的关系。
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