射血分数保留的心力衰竭患者在接受中枢和外周化学感受器刺激时出现异常的神经血管控制。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-06-01 Epub Date: 2024-06-15 DOI:10.1007/s10286-024-01041-4
Yufuko Kataoka, Allan R K Sales, Amanda G Rodrigues, Beatriz R Goes-Santos, Luciene F Azevedo, Raphaela V Groehs, Edna O Silva, Luciana S Santos, Patricia A Oliveira, Camila P Jordão, Ana C M Andrade, Denise M L Lobo, Eduardo Rondon, Edgar Toschi-Dias, Maria Janieire N N Alves, Dirceu R Almeida, Carlos E Negrão
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引用次数: 0

摘要

目的:射血分数降低型心力衰竭患者的中枢和外周化学感受器过敏。至于射血分数保留型心力衰竭(HFpEF)患者是否也会发生这种自律神经改变,目前仍知之甚少。我们检验了一个假设,即射血分数保留型心力衰竭患者中枢和外周化学反射对肌肉交感神经活动(MSNA)的控制发生了改变:研究对象包括年龄 55-80 岁、有心力衰竭症状、体重指数≤ 35 kg/m2、左室射血分数 > 50%、左房容积指数 > 34 mL/m2、左室舒张早期充盈速度和二尖瓣环舒张早期组织速度比值(E/e'指数)≥ 13、BNP 水平 > 35 pg/mL的患者(HFpEF,n = 9)。无射血分数保留型心力衰竭的患者(非 HFpEF,n = 9)也被纳入研究,年龄配对。外周化学感受器刺激(10% 氧气和 90% 氮气,二氧化碳滴定)和中枢化学感受器刺激(7% 二氧化碳和 93% 氧气)持续 3 分钟。用微神经电图技术评估 MSNA,用静脉阻塞血压计评估前臂血流量(FBF):结果:缺氧时,MSNA 反应更大(P高频低氧血症患者的外周和中枢化学反射对 MSNA 的控制过敏,这似乎是导致这些患者 MSNA 增加的原因。此外,HFpEF 患者的外周和中枢化学感受器刺激会导致肌肉血管收缩。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Abnormal neurovascular control during central and peripheral chemoreceptors stimulation in heart failure patients with preserved ejection fraction.

Abnormal neurovascular control during central and peripheral chemoreceptors stimulation in heart failure patients with preserved ejection fraction.

Purpose: Central and peripheral chemoreceptors are hypersensitized in patients with heart failure with reduced ejection fraction. Whether this autonomic alteration occurs in patients with heart failure with preserved ejection fraction (HFpEF) remains little known. We test the hypothesis that the central and peripheral chemoreflex control of muscle sympathetic nerve activity (MSNA) is altered in HFpEF.

Methods: Patients aged 55-80 years with symptoms of heart failure, body mass index ≤ 35 kg/m2, left ventricular ejection fraction > 50%, left atrial volume index > 34 mL/m2, left ventricular early diastolic filling velocity and early diastolic tissue velocity of mitral annulus ratio (E/e' index) ≥ 13, and BNP levels > 35 pg/mL were included in the study (HFpEF, n = 9). Patients without heart failure with preserved ejection fraction (non-HFpEF, n = 9), aged-paired, were also included in the study. Peripheral chemoreceptors stimulation (10% O2 and 90% N2, with CO2 titrated) and central chemoreceptors stimulation (7% CO2 and 93% O2) were conducted for 3 min. MSNA was evaluated by microneurography technique, and forearm blood flow (FBF) by venous occlusion plethysmography.

Results: During hypoxia, MSNA responses were greater (p < 0.001) and FBF responses were lower in patients with HFpEF (p = 0.006). Likewise, MSNA responses during hypercapnia were higher (p < 0.001) and forearm vascular conductance (FVC) levels were lower (p = 0.030) in patients with HFpEF.

Conclusions: Peripheral and central chemoreflex controls of MSNA are hypersensitized in patients with HFpEF, which seems to contribute to the increase in MSNA in these patients. In addition, peripheral and central chemoreceptors stimulation in patients with HFpEF causes muscle vasoconstriction.

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