Chen Horng H, Sundt Thoralf M, Cook David J, Heublein Denise M, Burnett John C
Department of Internal Medicine and Division of Cardiovascular Diseases, Mayo Clinic and Foundation, 200 First St SW, Rochester, MN 55905, USA.
Circulation. 2007 Sep 11;116(11 Suppl):I134-8. doi: 10.1161/CIRCULATIONAHA.106.697250.
Renal insufficiency is associated with increased morbidity and mortality after cardiopulmonary bypass cardiac surgery. B-type natriuretic peptide is a cardiac hormone that enhances glomerular filtration rate and inhibits aldosterone. Cystatin has been shown to be a better endogenous marker of renal function than creatinine.
We performed a double-blinded placebo-controlled proof of concept pilot study in patients (n=40) with renal insufficiency preoperatively (defined as an estimated creatinine clearance of <60 mL/min determined by the Cockroft-Gault formula), undergoing cardiopulmonary bypass cardiac surgery. Patients were randomized to placebo (n=20) or i.v. low dose nesiritide (n=20; 0.005 microg/Kg/min) for 24 hours started after the induction of anesthesia and before cardiopulmonary bypass. Patients in the nesiritide group had an increase of plasma B-type natriuretic peptide and its second messenger cGMP with a decrease in plasma cystatin levels at the end of the 24-hour infusion. These changes were not observed in the placebo group. There was a significant activation of aldosterone in the placebo group at the end of the 24-hour infusion, but not in the nesiritide group. At 48 and 72 hours, there was a decrease in estimated creatinine clearance and an increase in plasma cystatin as compared with end of the 24-hour infusion in the placebo group. In contrast, renal function was preserved in the nesiritide group with no significant change in estimated creatinine clearance and a trend for plasma cystatin to increase as compared with end of the 24-hour infusion.
This proof of concept pilot study supports the conclusion that perioperative administration of low dose nesiritide is biologically active and decreases plasma cystatin in patients with renal insufficiency undergoing cardiopulmonary bypass cardiac surgery. Further studies are warranted to determine whether these physiological observations can be translated into improved clinical outcomes.
肾功能不全与体外循环心脏手术后发病率和死亡率增加相关。B型利钠肽是一种心脏激素,可提高肾小球滤过率并抑制醛固酮。胱抑素已被证明是比肌酐更好的肾功能内源性标志物。
我们对术前肾功能不全(根据Cockcroft-Gault公式定义为估计肌酐清除率<60 mL/分钟)且接受体外循环心脏手术的患者(n = 40)进行了一项双盲安慰剂对照概念验证性初步研究。患者被随机分为安慰剂组(n = 20)或静脉注射低剂量奈西立肽组(n = 20;0.005微克/千克/分钟),从麻醉诱导后且在体外循环前开始持续24小时。奈西立肽组患者在24小时输注结束时血浆B型利钠肽及其第二信使cGMP增加,血浆胱抑素水平降低。安慰剂组未观察到这些变化。安慰剂组在24小时输注结束时醛固酮有显著激活,而奈西立肽组未出现。与24小时输注结束时相比,安慰剂组在48小时和72小时时估计肌酐清除率降低,血浆胱抑素增加。相比之下,奈西立肽组肾功能得以保留,估计肌酐清除率无显著变化,与24小时输注结束时相比血浆胱抑素呈增加趋势。
这项概念验证性初步研究支持以下结论,即围手术期给予低剂量奈西立肽具有生物学活性,并可降低接受体外循环心脏手术的肾功能不全患者的血浆胱抑素水平。有必要进行进一步研究以确定这些生理观察结果是否能转化为改善的临床结局。