Department of Disease Control and Homeostasis, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
Department of Disease Control and Homeostasis, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
Auton Neurosci. 2018 Sep;213:8-14. doi: 10.1016/j.autneu.2018.04.006. Epub 2018 Apr 30.
Augmented sympathetic nerve activity is associated with heart failure with preserved left ventricular ejection fraction (HFpEF). Lipophilic statins reduce sympathetic nerve activity in patients with heart failure with reduced left ventricular ejection fraction. However, little is known about whether all types of statins, regardless of solubility, reduce sympathetic nerve activity in HFpEF. We evaluated the effect of atorvastatin, a lipophilic statin, and rosuvastatin, a hydrophilic statin, on muscle sympathetic nerve activity (MSNA) in HFpEF patients. This study was conducted as a prospective, randomized, open-label, crossover trial. Ten HFpEF patients with untreated hyperlipidemia participated in this study. Subjects were assigned to either the atorvastatin (lipophilic) or the rosuvastatin (hydrophilic) group with each drug administered for 8 weeks. Atorvastatin and rosuvastatin treatment resulted in a similar reduction in low-density lipoprotein cholesterol (LDL-C) levels. There was no difference in the effect of either treatment on blood pressure, heart rate, or left ventricular function. Atorvastatin significantly decreased MSNA frequency compared with baseline (31.5 ± 6.3 vs. 47.5 ± 10.7 bursts/min, p < 0.01), but rosuvastatin had no effect on MSNA (40.9 ± 7.3 bursts/min). MSNA was significantly lower in the atorvastatin group than rosuvastatin group (p < 0.05). However, the reduction in MSNA seen in either group did not correlate with the reduction in LDL-C. No significant differences were observed in either the baroreflex control of heart rate or MSNA between the two groups. These results suggest that lipophilic statins have a favorable effect on sympathetic nerve activity beyond lowering LDL-C in HFpEF, but hydrophilic statins do not.
交感神经活性增强与射血分数保留的心力衰竭(HFpEF)有关。亲脂性他汀类药物可降低射血分数降低的心力衰竭患者的交感神经活性。然而,对于所有类型的他汀类药物,无论其亲脂性如何,是否都能降低 HFpEF 患者的交感神经活性,目前知之甚少。我们评估了亲脂性阿托伐他汀和亲水性瑞舒伐他汀对 HFpEF 患者肌肉交感神经活性(MSNA)的影响。这项研究是作为一项前瞻性、随机、开放标签、交叉试验进行的。10 例未经治疗的高脂血症 HFpEF 患者参加了这项研究。受试者被分为阿托伐他汀(亲脂性)或瑞舒伐他汀(亲水性)组,每组药物治疗 8 周。阿托伐他汀和瑞舒伐他汀治疗均可使 LDL-C 水平显著降低。两种药物对血压、心率或左心室功能均无影响。与基线相比,阿托伐他汀显著降低 MSNA 频率(31.5±6.3 比 47.5±10.7 次/分,p<0.01),但瑞舒伐他汀对 MSNA 无影响(40.9±7.3 次/分)。阿托伐他汀组的 MSNA 明显低于瑞舒伐他汀组(p<0.05)。然而,两组中 MSNA 的降低与 LDL-C 的降低无关。两组间心率及 MSNA 的压力反射控制均无显著差异。这些结果表明,亲脂性他汀类药物除了降低 LDL-C 外,对 HFpEF 患者的交感神经活性有有利影响,而亲水性他汀类药物则没有。