Hillock R J, Frampton C M, Yandle T G, Troughton R W, Lainchbury J G, Richards A M
Christchurch Cardioendocrine Research Group, Christchurch School of Medicine and Health Sciences and Christchurch Hospital, Christchurch, New Zealand.
Heart. 2008 May;94(5):617-22. doi: 10.1136/hrt.2006.110239. Epub 2007 Jul 16.
Natriuretic peptides have actions likely to ameliorate cardiac dysfunction. B-type natriuretic peptide (BNP) is indicated as treatment for decompensated cardiac failure.
To determine the utility of BNP in acute myocardial infarction (MI).
Double-blind randomised placebo-controlled trial.
Tertiary hospital coronary care unit.
28 patients with acute MI with delayed or failed reperfusion and moderate left ventricular dysfunction.
Infusion of BNP or placebo for 60 hours after MI.
Neurohormonal activation and renal function in response to BNP infusion, secondary end points of echocardiographic measures of left ventricular function and dimension.
BNP infusion resulted in a significant rise in BNP (276 pg/l vs 86 pg/l, p = 0.001). NT-proBNP levels were suppressed by BNP infusion (p = 0.002). Atrial natriuretic peptide (ANP) and NT-proANP levels fell with a significant difference in the pattern between BNP infusion and placebo during the first 5 days (p<0.005). C-type natriuretic peptide (CNP) and NT-proCNP levels rose during the infusion with higher levels than placebo at all measurements during the first 3 days (p<0.01). Cyclic guanosine monophosphate (cGMP) was raised during the infusion period showing a peak of 23 pmol/l on day 2 (placebo 8.9 pmol/l, p = 0.002), with a correlation between BNP and cGMP levels (p<0.001). Glomerular filtration rate (GFR) fell with BNP infusion but was not significantly lower than with placebo (71.0 (5.6) vs 75.8 (5.4) ml/min/1.73 m2, p = 0.62). Patients receiving nesiritide exhibited favourable trends in left ventricular remodelling.
Nesiritide, given soon after MI, induced increments in plasma cGMP and CNP and decrements in other endogenous cardiac peptides with a neutral effect on renal function and a trend towards favourable ventricular remodelling.
利钠肽具有改善心脏功能障碍的作用。B型利钠肽(BNP)被用作失代偿性心力衰竭的治疗药物。
确定BNP在急性心肌梗死(MI)中的作用。
双盲随机安慰剂对照试验。
三级医院冠心病监护病房。
28例急性MI患者,再灌注延迟或失败,伴有中度左心室功能障碍。
MI后60小时输注BNP或安慰剂。
输注BNP后的神经激素激活和肾功能,左心室功能和大小的超声心动图测量的次要终点。
输注BNP导致BNP显著升高(276 pg/l对86 pg/l,p = 0.001)。NT-proBNP水平被BNP输注抑制(p = 0.002)。在前5天内,心房利钠肽(ANP)和NT-proANP水平下降,BNP输注组和安慰剂组的下降模式有显著差异(p<0.005)。C型利钠肽(CNP)和NT-proCNP水平在输注期间升高,在前3天的所有测量中均高于安慰剂组(p<0.01)。环磷酸鸟苷(cGMP)在输注期间升高,在第2天达到峰值23 pmol/l(安慰剂组为8.9 pmol/l,p = 0.002),BNP与cGMP水平之间存在相关性(p<0.001)。肾小球滤过率(GFR)在输注BNP后下降,但不显著低于安慰剂组(71.0(5.6)对75.8(5.4)ml/min/1.73 m2,p = 0.62)。接受奈西立肽治疗的患者在左心室重构方面呈现出有利趋势。
MI后早期给予奈西立肽可使血浆cGMP和CNP升高,其他内源性心脏肽降低,对肾功能无明显影响,并具有改善心室重构的趋势。