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口服酮酯治疗射血分数降低的心力衰竭患者的心血管效应:一项随机、对照、双盲试验。

Cardiovascular Effects of Oral Ketone Ester Treatment in Patients With Heart Failure With Reduced Ejection Fraction: A Randomized, Controlled, Double-Blind Trial.

机构信息

Department of Cardiology (K.B.-H., N.G., K.H.C., B.L., M.J.A., S.H.P., R.N., H.W.), Aarhus University Hospital, Denmark.

Department of Clinical Medicine, Faculty of Health, Aarhus University, Denmark (K.B.-H., N.G., K.H.C., B.L., S.H.P., N.M., H.W.).

出版信息

Circulation. 2024 May 7;149(19):1474-1489. doi: 10.1161/CIRCULATIONAHA.123.067971. Epub 2024 Mar 27.

Abstract

BACKGROUND

Heart failure triggers a shift in myocardial metabolic substrate utilization, favoring the ketone body 3-hydroxybutyrate as energy source. We hypothesized that 14-day treatment with ketone ester (KE) would improve resting and exercise hemodynamics and exercise capacity in patients with heart failure with reduced ejection fraction.

METHODS

In a randomized, double-blind cross-over study, nondiabetic patients with heart failure with reduced ejection fraction received 14-day KE and 14-day isocaloric non-KE comparator regimens of 4 daily doses separated by a 14-day washout period. After each treatment period, participants underwent right heart catheterization, echocardiography, and blood sampling at plasma trough levels and after dosing. Participants underwent an exercise hemodynamic assessment after a second dosing. The primary end point was resting cardiac output (CO). Secondary end points included resting and exercise pulmonary capillary wedge pressure and peak exercise CO and metabolic equivalents.

RESULTS

We included 24 patients with heart failure with reduced ejection fraction (17 men; 65±9 years of age; all White). Resting CO at trough levels was higher after KE compared with isocaloric comparator (5.2±1.1 L/min versus 5.0±1.1 L/min; difference, 0.3 L/min [95% CI, 0.1-0.5), and pulmonary capillary wedge pressure was lower (8±3 mm Hg versus 11±3 mm Hg; difference, -2 mm Hg [95% CI, -4 to -1]). These changes were amplified after KE dosing. Across all exercise intensities, KE treatment was associated with lower mean exercise pulmonary capillary wedge pressure (-3 mm Hg [95% CI, -5 to -1] ) and higher mean CO (0.5 L/min [95% CI, 0.1-0.8]), significantly different at low to moderate steady-state exercise but not at peak. Metabolic equivalents remained similar between treatments. In exploratory analyses, KE treatment was associated with 18% lower NT-proBNP (N-terminal pro-B-type natriuretic peptide; difference, -98 ng/L [95% CI, -185 to -23]), higher left ventricular ejection fraction (37±5 versus 34±5%; =0.01), and lower left atrial and ventricular volumes.

CONCLUSIONS

KE treatment for 14 days was associated with higher CO at rest and lower filling pressures, cardiac volumes, and NT-proBNP levels compared with isocaloric comparator. These changes persisted during exercise and were achieved on top of optimal medical therapy. Sustained modulation of circulating ketone bodies is a potential treatment principle in patients with heart failure with reduced ejection fraction.

REGISTRATION

URL: https://www.clinicaltrials.gov; Unique identifier: NCT05161650.

摘要

背景

心力衰竭会引发心肌代谢底物利用的转变,有利于酮体 3-羟基丁酸作为能量来源。我们假设,酮酯(KE)治疗 14 天可改善射血分数降低的心力衰竭患者的静息和运动血液动力学及运动能力。

方法

在一项随机、双盲交叉研究中,射血分数降低的心力衰竭的非糖尿病患者接受了 14 天的 KE 和 14 天等热量非 KE 对照治疗方案,每天 4 次剂量,间隔 14 天洗脱期。在每个治疗期后,参与者在血浆谷水平和给药后进行右心导管检查、超声心动图和血液采样。在第二次给药后,参与者进行了运动血液动力学评估。主要终点是静息心输出量(CO)。次要终点包括静息和运动肺毛细血管楔压以及峰值运动 CO 和代谢当量。

结果

我们纳入了 24 名射血分数降低的心力衰竭患者(17 名男性;65±9 岁;均为白人)。KE 组在谷水平时的静息 CO 高于等热量对照(5.2±1.1 L/min 与 5.0±1.1 L/min;差异为 0.3 L/min [95%CI,0.1-0.5]),肺毛细血管楔压更低(8±3 mm Hg 与 11±3 mm Hg;差异为-2 mm Hg [95%CI,-4 至-1])。这些变化在 KE 给药后放大。在所有运动强度下,KE 治疗与较低的平均运动肺毛细血管楔压(-3 mm Hg [95%CI,-5 至-1])和较高的平均 CO(0.5 L/min [95%CI,0.1-0.8])相关,在低至中度稳定运动时差异显著,但在峰值时无差异。两种治疗方法的代谢当量保持相似。在探索性分析中,KE 治疗与 N 端脑利钠肽前体(NT-proBNP)降低 18%相关(差值为-98 ng/L [95%CI,-185 至-23]),左心室射血分数升高(37±5 与 34±5%;=0.01),左心房和心室容积降低。

结论

与等热量对照相比,KE 治疗 14 天可使静息时 CO 升高,充盈压、心脏容积和 NT-proBNP 水平降低。这些变化在运动期间持续存在,并在最佳药物治疗的基础上得以实现。持续调节循环酮体可能是射血分数降低的心力衰竭患者的一种潜在治疗原则。

登记

网址:https://www.clinicaltrials.gov;唯一标识符:NCT05161650。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c18/11081479/f24cc110ebdf/cir-149-1474-g001.jpg

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