Aronson Doron, Burger Andrew J
Division of Cardiology, Rambam Medical Center, Haifa, Israel.
Am Heart J. 2004 Nov;148(5):e16. doi: 10.1016/j.ahj.2004.05.027.
Previous studies have suggested that natriuretic peptides may have direct sympathoinhibitory effects. Nesiritide (recombinant human B-type natriuretic peptide) has been recently approved for treatment of decompensated congestive heart failure (CHF). We sought to assess the effects of nesiritide compared with dobutamine on time-domain indices of heart rate variability (HRV) in patients with decompensated CHF.
The study population consisted of 185 patients, who were randomized to intravenous nesiritide at a low (0.015 microg/kg/min, n = 56) or high (0.03 microg/kg/min, n = 58) dose, or to dobutamine (> or = 5 microg/kg/min, n = 58). Time-domain HRV indices were obtained from 24-hour Holter recordings immediately before and during study drug therapy.
Dobutamine therapy resulted in a decrease in standard deviation of the R-R intervals over a 24-hour period (SDNN), standard deviation of all 5-minute mean R-R intervals (SDANN), and the percentage of R-R intervals with >50 ms variation (pNN50) (all P < .05). Low-dose nesiritide induced an increase in SDNN (P < .05), and high-dose nesiritide resulted in a nonsignificant decrease in all measures of HRV. A significant interaction was noted between baseline HRV and the effect of vasoactive therapy on HRV (P = .028). Therefore, the effect of nesiritide and dobutamine was analyzed in relation to baseline HRV. In the dobutamine group, patients with moderately depressed HRV at baseline displayed a reduction in SDNN (P = .01), SDANN (P = .01), pNN50 (P = .04), and the square root of mean squared differences of successive R-R intervals (RMSSD) (P = .05), whereas no significant changes occurred in patients with severely depressed HRV. In the low-dose nesiritide group, patients with severely depressed HRV displayed an increase in SDNN (P = .001), SDANN (P = .02), and RMSSD (P = .01), with no significant changes in patients with moderately depressed HRV. HRV response to high-dose nesiritide was similar to that of dobutamine.
Low-dose nesiritide therapy in patients with decompensated CHF improves indices of overall HRV and parasympathetic modulation, particularly if HRV is severely depressed at baseline. Dobutamine and possibly high-dose nesiritide can potentially lead to further deterioration of autonomic dysregulation.
既往研究提示利钠肽可能具有直接的交感神经抑制作用。奈西立肽(重组人B型利钠肽)最近已被批准用于治疗失代偿性充血性心力衰竭(CHF)。我们旨在评估奈西立肽与多巴酚丁胺相比对失代偿性CHF患者心率变异性(HRV)时域指标的影响。
研究人群包括185例患者,他们被随机分为低剂量(0.015μg/kg/min,n = 56)或高剂量(0.03μg/kg/min,n = 58)静脉注射奈西立肽组,或多巴酚丁胺组(≥5μg/kg/min,n = 58)。在研究药物治疗前及治疗期间,通过24小时动态心电图记录获取时域HRV指标。
多巴酚丁胺治疗导致24小时内R-R间期标准差(SDNN)、所有5分钟平均R-R间期标准差(SDANN)以及R-R间期变化>50ms的百分比(pNN50)降低(均P <.05)。低剂量奈西立肽使SDNN升高(P <.05),高剂量奈西立肽导致所有HRV指标出现非显著性降低。观察到基线HRV与血管活性治疗对HRV的影响之间存在显著交互作用(P = 0.028)。因此,分析了奈西立肽和多巴酚丁胺相对于基线HRV的效应。在多巴酚丁胺组中,基线时HRV中度降低的患者SDNN(P = 0.01)、SDANN(P = 0.01)、pNN50(P = 0.04)以及连续R-R间期均方根差值(RMSSD)(P = 0.05)降低,而HRV严重降低的患者无显著变化。在低剂量奈西立肽组中,HRV严重降低的患者SDNN(P = 0.001)、SDANN(P = 0.02)和RMSSD(P = 0.01)升高,HRV中度降低的患者无显著变化。高剂量奈西立肽的HRV反应与多巴酚丁胺相似。
失代偿性CHF患者接受低剂量奈西立肽治疗可改善整体HRV指标和副交感神经调节,特别是如果基线时HRV严重降低。多巴酚丁胺以及可能的高剂量奈西立肽可能会导致自主神经调节异常进一步恶化。