Skvortsov A A, Mareev V Iu, Nasonova S N, Sychev A V, Arbolishvili G N, Baklanova N A, Masenko V P, Belenkov Iu N
Ter Arkh. 2006;78(9):61-71.
To assess different variants of neurohormonal (NH) modulation with angiotensin converting enzyme (ACE-I) quinapril (Q), angiotensin-receptor blocker (ARB) valsartan (V) and their combination in addition to beta-adrenergic blocker bisoprolol (B) on functional status, quality of life (QL), parameters of left ventricular (LP) remodeling, main indices of 24-h heart rate variability (HRV) and NH profile in patients with stable mild-to-moderate CHF.
63 patients with CHF (NYHA class II-III) as a result of ischemic heart disease and dilated cardiomyopathy with LV EF < 40% were randomly assigned to one of the treatment variants on 1:1:1 basis: B+Q (n = 22; mean daily dose of B-5.5 mg; Q-15.4 mg), B+V (n = 23; mean daily dose of B = 4.8 mg; V = 128 mg) and combination of B+Q+V (n = 18; mean daily dose of B = 4.1 mg; Q = 12 mg; V = 82 mg). At baseline, all the patients in this study were on background B treatment and according to the study design Q or V were then added to B at randomization. NYHA FC, 6-min walking test (6MT), QL, 2D-echocardiography, plasma rennin activity (PRA), angiotensin II (AT-II), aldosterone (Ald), norepinephrine (NE), epinephrine (E), brain natriuretic peptide (BNP) concentrations and 24-hour HRV parameters were investigated at baseline, 3 and 6 months after randomization.
During the study NYHA FC improvement was revealed in all 3 treatment groups with comparative significant changes in 6MT distance by 20.4%, 19.1% and 19.4% in B+Q, B+V and B+Q+V groups. QL maximally decreased in B+V combination (from 45 to 21 points). LV volumes significantly decreased and LV ejection fraction (EF) increased in all groups to the end of the study. Triple combination had no additional effect on LV volumes and LVEF changes compared to B+Q and B+V groups. Maximally plasma NE concentrations decreased in B+Q group (from 650 to 430 pg/ml, p = 0.007). A worse effect was observed in the combination of B+Q+V, with any NE changes in B+V group. The E concentration increased significantly (from 215 to 295 pg/ml, p = 0.024) in the B+Q+V group at the end of the study. Plasma A-H concentration did not differ from the baseline during the study in B+Q group, but significantly increased in B+V group and maximally in B+Q+V group (from 11.4 to 23.5 pg/ml, p = 0.009). To the end of the study plasma Ald concentrations remain reduced significantly only in B+V group. The level of BNP significantly decreased in all 3 treatment groups. Significant changes in HRV indices, both in time and frequency domain, were revealed in the B+Q group at 3-month follow-up and SDNN increased on month 24 (p = 0.039). These changes became insignificant at the end of the study. The lesser effect was revealed in B+Q+V group, with insignificant trend toward an increase of SDNN to the end of the study. HRV indices did not improve in the B+V group.
During long-term treatment the triple combination of B+Q+V has no significant advantages over B+Q and B+V by the functional status, QL and parameters of LV remodeling in patients with mild-to-moderate CHF. The combination of B+Q has more potent effect on 24-hour HRV parameters, sympatho-adrenal activity and renal function compared to B+V and B+Q+V groups in CHF patients in our study. The combination B+Q+V may have a negative effect on NH profile (excessive activation of ATII and E) in CHF patients. The triple combination is not recommended for therapy of stable mild-to-moderate CHF patients.
评估血管紧张素转换酶抑制剂(ACE-I)喹那普利(Q)、血管紧张素受体阻滞剂(ARB)缬沙坦(V)及其联合用药,以及β-肾上腺素能阻滞剂比索洛尔(B)对稳定的轻至中度慢性心力衰竭(CHF)患者功能状态、生活质量(QL)、左心室(LV)重构参数、24小时心率变异性(HRV)主要指标和神经激素(NH)谱的不同影响。
63例因缺血性心脏病和扩张型心肌病导致CHF(纽约心脏协会心功能分级II-III级)且左室射血分数(LV EF)<40%的患者,按1:1:1比例随机分配至以下治疗组之一:B+Q组(n = 22;B平均日剂量5.5 mg;Q平均日剂量15.4 mg)、B+V组(n = 23;B平均日剂量4.8 mg;V平均日剂量128 mg)和B+Q+V联合组(n = 18;B平均日剂量4.1 mg;Q平均日剂量12 mg;V平均日剂量82 mg)。基线时,本研究所有患者均接受B治疗,根据研究设计,随机分组时将Q或V加至B治疗中。在基线、随机分组后3个月和6个月时,对纽约心脏协会心功能分级(NYHA FC)、6分钟步行试验(6MT)、QL、二维超声心动图、血浆肾素活性(PRA)、血管紧张素II(AT-II)、醛固酮(Ald)、去甲肾上腺素(NE)、肾上腺素(E)、脑钠肽(BNP)浓度及24小时HRV参数进行研究。
研究期间,所有3个治疗组的NYHA FC均有改善,B+Q组、B+V组和B+Q+V组的6MT距离分别有20.4%、19.1%和19.4%的比较显著变化。B+V联合组的QL下降最大(从45分降至21分)。至研究结束时,所有组的LV容积均显著减小,左室射血分数(EF)增加。与B+Q组和B+V组相比,三联组合对LV容积和LVEF变化无额外影响。B+Q组的血浆NE浓度下降最大(从650 pg/ml降至430 pg/ml,p = 0.007)。B+Q+V联合组效果较差,B+V组的NE无变化。研究结束时,B+Q+V组的E浓度显著升高(从215 pg/ml升至295 pg/ml,p = 0.024)。研究期间,B+Q组的血浆A-H浓度与基线无差异,但B+V组显著升高,B+Q+V组升高最大(从'11.4 pg/ml升至23.5 pg/ml,p = 0.009)。至研究结束时,仅B+V组的血浆Ald浓度仍显著降低。所有3个治疗组的BNP水平均显著下降。B+Q组在3个月随访时HRV指标在时域和频域均有显著变化,且24个月时的标准偏差(SDNN)增加(p = 0.039)。这些变化在研究结束时变得不显著。B+Q+V组效果较差,至研究结束时SDNN有不显著的增加趋势。B+V组的HRV指标未改善。
在轻至中度CHF患者中,长期治疗时B+Q+V三联组合在功能状态、QL和LV重构参数方面相对于B+Q组和B+V组无显著优势。在本研究的CHF患者中,与B+V组和B+Q+V组相比,B+Q联合用药对24小时HRV参数、交感-肾上腺活动和肾功能有更强的作用。B+Q+V联合用药可能对CHF患者的NH谱有负面影响(ATII和E过度激活)。不推荐三联组合用于稳定的轻至中度CHF患者的治疗。