Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.
Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts.
J Am Coll Cardiol. 2019 Mar 26;73(11):1273-1284. doi: 10.1016/j.jacc.2018.12.063.
With sacubitril/valsartan treatment, B-type natriuretic peptide (BNP) concentrations increase; it remains unclear whether change in BNP concentrations is similar across all assays for its measurement. Effects of sacubitril/valsartan on atrial natriuretic peptide (ANP) concentrations in patients are unknown. Lastly, the impact of neprilysin inhibition on mid-regional pro-ANP (MR-proANP), N-terminal pro-BNP (NT-proBNP), proBNP, or C-type natriuretic peptide (CNP) is not well understood.
This study sought to examine the effects of sacubitril/valsartan on results from different natriuretic peptide assays.
Twenty-three consecutive stable patients with heart failure and reduced ejection fraction were initiated and titrated on sacubitril/valsartan. Change in ANP, MR-proANP, BNP (using 5 assays), NT-proBNP (3 assays), proBNP, and CNP were measured over 3 visits.
Average time to 3 follow-up visits was 22, 46, and 84 days. ANP rapidly and substantially increased with initiation and titration of sacubitril/valsartan, more than doubling by the first follow-up visit (+105.8%). Magnitude of ANP increase was greatest in those with concentrations above the median at baseline (+188%) compared with those with lower baseline concentrations (+44%); ANP increases were sustained. Treatment with sacubitril/valsartan led to inconsistent changes in BNP, which varied across methods assessed. Concentrations of MR-proANP, NT-proBNP, and proBNP variably declined after treatment; whereas CNP concentrations showed no consistent change.
Initiation and titration of sacubitril/valsartan led to variable changes in concentrations of multiple natriuretic peptides. These results provide important insights into the effects of sacubitril/valsartan treatment on individual patient results, and further suggest the benefit of neprilysin inhibition may be partially mediated by increased ANP concentrations.
沙库巴曲缬沙坦治疗后,B 型利钠肽(BNP)浓度升高;但其测量的所有检测方法中 BNP 浓度的变化是否相似尚不清楚。沙库巴曲缬沙坦对心房利钠肽(ANP)浓度在患者中的影响尚不清楚。最后,脑啡肽酶抑制对中段利钠肽前体(MR-proANP)、N 末端 pro-BNP(NT-proBNP)、proBNP 或 C 型利钠肽(CNP)的影响尚不清楚。
本研究旨在研究沙库巴曲缬沙坦对不同利钠肽检测结果的影响。
连续纳入 23 例稳定的射血分数降低的心力衰竭患者,给予沙库巴曲缬沙坦起始治疗和滴定治疗。在 3 次就诊时测量 ANP、MR-proANP、BNP(使用 5 种检测方法)、NT-proBNP(3 种检测方法)、proBNP 和 CNP 的变化。
平均 3 次随访时间为 22、46 和 84 天。随着沙库巴曲缬沙坦的起始和滴定治疗,ANP 迅速且大幅升高,在首次随访时增加了一倍以上(+105.8%)。与基线时浓度较低的患者(+44%)相比,基线时浓度处于中位数以上的患者(+188%)的 ANP 增加幅度更大;ANP 增加持续存在。沙库巴曲缬沙坦治疗导致 BNP 的变化不一致,这在评估的各种方法中都有所不同。MR-proANP、NT-proBNP 和 proBNP 的浓度在治疗后不同程度下降;而 CNP 浓度没有一致变化。
沙库巴曲缬沙坦的起始和滴定治疗导致多种利钠肽浓度的变化。这些结果为沙库巴曲缬沙坦治疗对个体患者结果的影响提供了重要的见解,并进一步表明脑啡肽酶抑制的益处可能部分通过增加 ANP 浓度介导。