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(8):14-20.
To assess effects of 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 (QOL), parameters of left ventricular (LV) remodeling, main indices of 24-h heart rate variability (HRV) and NH profile in patients with stable mild-to-moderate congestive heart failure (CHF).
Sixty three 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), B+V (n = 23) and combination of B+Q + V (n = 18). 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), QOL, 2D-echocardiography, plasma renin 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 three 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, respectively. QOL 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. Plasma NE concentrations decreased maximally in B+Q group (from 650 to 430 pg/ml, p = 0.007). The lesser 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-II 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, QOL 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)及其与β-肾上腺素能阻滞剂比索洛尔(B)联合使用的不同神经激素(NH)调节变体,对稳定的轻至中度充血性心力衰竭(CHF)患者的功能状态、生活质量(QOL)、左心室(LV)重构参数、24小时心率变异性(HRV)主要指标和NH谱的影响。
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II-III级)且LV EF<40%的患者,按1:1:1随机分配至以下治疗变体之一:B+Q(n = 22)、B+V(n = 23)和B+Q + V联合治疗(n = 18)。基线时,本研究所有患者均接受基础B治疗,根据研究设计,随机将Q或V添加到B治疗中。在基线、随机分组后3个月和6个月时,对纽约心脏协会功能分级(NYHA FC)、6分钟步行试验(6MT)、QOL、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)浓度和24小时HRV参数进行研究。
在研究期间,所有三个治疗组的NYHA FC均有改善,B+Q、B+V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联合治疗组的QOL下降最大(从45分降至21分)。到研究结束时,所有组的LV容积均显著减小,LV射血分数(EF)增加。与B+Q和B+V组相比,三联组合对LV容积和LVEF变化没有额外影响。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联合治疗组的效果较小,B+V组的NE无变化。在研究结束时,B+Q+V组的E浓度显著增加(从215 pg/ml增至295 pg/ml,p = 0.024)。在研究期间,B+Q组的血浆A-II浓度与基线无差异,但在B+V组显著增加,在B+Q+V组增加最大(从11.4 pg/ml增至23.5 pg/ml,p = 0.009)。到研究结束时,仅B+V组的血浆Ald浓度仍显著降低。所有3个治疗组的BNP水平均显著降低。在3个月随访时,B+Q组的HRV指标在时域和频域均有显著变化,且在第24个月时SDNN增加(p = 0.039)。这些变化在研究结束时变得不显著。B+Q+V组的效果较小,到研究结束时SDNN有增加但不显著的趋势。B+V组的HRV指标未改善。
在轻至中度CHF患者中,长期治疗期间,B+Q+V三联组合在功能状态、QOL和LV重构参数方面,与B+Q和B+V相比无显著优势。在本研究的CHF患者中,与B+V和B+Q+V组相比,B+Q组合对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组合可能对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。