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血管紧张素受体/脑啡肽酶抑制剂治疗慢性收缩性心力衰竭后生物活性肾上腺髓质素浓度升高。

Increased concentrations of bioactive adrenomedullin subsequently to angiotensin-receptor/neprilysin-inhibitor treatment in chronic systolic heart failure.

机构信息

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Complexity Research, Vienna, Austria.

出版信息

Br J Clin Pharmacol. 2021 Mar;87(3):916-924. doi: 10.1111/bcp.14442. Epub 2020 Jul 20.

Abstract

AIMS

The clinically investigated rationale for neprilysin (NEP)-inhibition by angiotensinreceptor-NEPinhibitor (ARNi) therapy is to induce elevations in endogenous natriuretic peptides. NEP, however, cleaves a broad spectrum of substrates, which partially hold significant implications in heart failure with reduced ejection fraction (HFrEF). The effect of NEP inhibition on these peptides has not been investigated thoroughly. This study explored the response of adrenomedullin (ADM) regulation to the initiation of ARNi.

METHODS

Seventy-four patients with stable HFrEF and initiation of ARNi were prospectively enrolled, 67 patients on continuous angiotensin-converting-enzyme inhibitor(ACEi)/angiotensin-receptor blocker (ARB) therapy served as control. Plasma bioactive-ADM (bio-ADM), mid-regional-pro-ADM (MR-proADM), B-typenatriuretic peptide (BNP) and N-terminal-pro-BNP (NT-proBNP) were determined at baseline, short-term, 1-year and 2-year follow up.

RESULTS

Following ARNi initiation both bio-ADM and MR-proADM concentrations were significantly increased at early and long-term follow up (bio-ADM [pg/mL]: 26.0 [interquartile range {IQR}: 17.7-37.5] vs. 50.8 [IQR: 36.5-78.1] vs. 54.6 [IQR: 42.0-97.1] vs. 57.4 [IQR: 48.5-161.6]; MR-proADM [nmol/L]: 0.87 [IQR: 0.64-1.12] vs. 1.25 [IQR: 0.93-1.79] vs. 1.42 [IQR: 0.95-1.90] vs. 1.60 [IQR: 1.12-2.46], P < .0001 for all). The ratios bio-ADM/MR-proADM and BNP/NT-proBNP increased during ARNi-therapy proving improved availability of bioactive peptides. The proportional increase of bio-ADM markedly exceeded BNP increase. Patients converted to ARNi showed similar biomarker patterns irrespective of baseline renin-angiotensin system blocker therapy, i.e. ACEi or ARB (P > .05 for all), indicating that activation of the ADM-axis arises particularly from NEPinhibition.

CONCLUSION

The significant increase of MR-proADM and bio-ADM together with an elevated bioADM/MR-proADM ratio suggest both enhanced formation and reduced breakdown of bioactive ADM following the initiation of ARNi. Activation of the ADM-axis represents a so far unrecognized effect of ARNi.

摘要

目的

血管紧张素受体-脑啡肽酶抑制剂(ARNi)治疗通过抑制脑啡肽酶(NEP),使内源性利钠肽水平升高,这是临床研究中使用 NEP 抑制剂的基本原理。然而,NEP 可切割广泛的底物,其中部分在射血分数降低的心力衰竭(HFrEF)中具有重要意义。NEP 抑制对这些肽的影响尚未得到充分研究。本研究旨在探讨 NEP 抑制对肾上腺髓质素(ADM)调节的影响。

方法

前瞻性纳入 74 例稳定的射血分数降低的心力衰竭且开始使用 ARNi 的患者,以 67 例持续接受血管紧张素转换酶抑制剂(ACEi)/血管紧张素受体阻滞剂(ARB)治疗的患者作为对照。基线、短期、1 年和 2 年随访时测定生物活性 ADM(bio-ADM)、中段 pro-ADM(MR-proADM)、B 型利钠肽(BNP)和 N 端 pro-BNP(NT-proBNP)。

结果

ARNi 治疗后,早期和长期随访时 bio-ADM 和 MR-proADM 浓度均显著升高(bio-ADM[pg/ml]:26.0[四分位距{IQR}:17.7-37.5]vs.50.8[IQR:36.5-78.1]vs.54.6[IQR:42.0-97.1]vs.57.4[IQR:48.5-161.6];MR-proADM[nmol/L]:0.87[IQR:0.64-1.12]vs.1.25[IQR:0.93-1.79]vs.1.42[IQR:0.95-1.90]vs.1.60[IQR:1.12-2.46],所有 P 值均<.0001)。ARNi 治疗期间,bio-ADM/MR-proADM 和 BNP/NT-proBNP 比值升高,表明生物活性肽的可用性提高。bio-ADM 的比例增加明显超过 BNP 的增加。转换为 ARNi 的患者无论基线肾素-血管紧张素系统阻滞剂治疗(即 ACEi 或 ARB)如何,均表现出相似的生物标志物模式(所有 P 值均>.05),这表明 ADM 轴的激活特别源于 NEP 抑制。

结论

MR-proADM 和 bio-ADM 的显著增加以及 bioADM/MR-proADM 比值升高提示,ARNi 起始后,生物活性 ADM 的形成增加,而分解减少。ADM 轴的激活代表了 ARNi 的一种迄今尚未被认识到的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e3/9328655/b2ba13e863bb/BCP-87-916-g003.jpg

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