有氧运动对心脏的保护:一项随机试验。

IF 5.6
Claire Maufrais, Matthieu Josse, Laure Patrier, Myriam Isnard, Antoine Grandperrin, Cécile Turc-Baron, Stéphane Nottin, Jean-Paul Cristol, Doria Boulghobra, Cyril Reboul, Philippe Obert
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引用次数: 0

摘要

背景和假设:在血液透析(HD)期间,与短暂性缺血事件相关的左心室(LV)区域壁运动异常(RWMAs)已得到充分证明。分析内运动(IDE)减少了hd诱导的rwma的整体发生。然而,其在左室壁内的心脏保护作用的区域化及其潜在的机制尚不清楚。方法:我们进行了一项前瞻性、交叉、随机试验。72例患者接受了两个疗程:标准HD (HD- cont)和HD + 30分钟有氧运动(HD- ex)。在(T0)和峰值应力(hd结束前30min, Tpeak)时测量分段纵向应变(LS)。一个18段模型确定了rwma,定义为与T0相比,峰值时LS降低20%。为了评估循环因子的影响,我们测量了用人血浆超滤液预处理的分离大鼠心肌细胞在缺氧/再氧化(A/R)后的分数缩短,Ca2+瞬态和自发Ca2+波(SCaW)(在两次会议的Tpeak获得)。结果:与HD-CONT相比,IDE显著降低了HD-EX期间的rwma(估计差异:1.1段,95%CI: 0.33/1.90, p=0.009)。在HD-CONT期间观察到rwma的基底-根尖梯度,与根尖相比,根尖的患病率更高(p=0.03)。这种梯度在HD-EX期间被消除,表明有更大的心尖保护作用。与用HD-CONT超滤液预处理的细胞相比,用HD-EX超滤液预处理的心肌细胞改善了A/R后的分数缩短、Ca2+处理和SCaW。结论:IDE限制hd诱导的rwma,循环体液因子可能有助于这种心脏保护。ide诱导的rwma效益在顶端更大。需要进一步的研究来阐明IDE对局部心肌功能的异质性益处的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardioprotection from intradialytic exercise: a randomized trial.

Background and hypothesis: Left ventricular (LV) regional wall motion abnormalities (RWMAs) related to transient ischemic events are well-documented during hemodialysis (HD). Intradialytic exercise (IDE) reduces the global occurrence of HD-induced RWMAs. However, the regionalization of its cardioprotective effects within the LV wall, and its underlying mechanisms remain unclear.

Methods: We conducted a prospective, crossover, randomized trial. 72 patients underwent two sessions: standard HD (HD-CONT) and HD with 30min of aerobic exercise (HD-EX). Segmental longitudinal strains (LS) were measured before (T0) and at peak stress (30min before HD-ending, Tpeak). An 18-segment model identified RWMAs, defined as a 20% LS reduction at Tpeak compared to T0. To evaluate the impact of circulating factors, we measured fractional shortening, Ca2+ transients and spontaneous Ca2+ waves (SCaW) following anoxia/reoxygenation (A/R) in isolated rat cardiomyocytes pre-treated with human plasma ultrafiltrates (obtained at Tpeak in both sessions).

Results: IDE significantly reduced RWMAs during HD-EX compared to HD-CONT (estimated difference: 1.1 segment, 95%CI: 0.33/1.90, p=0.009). A baso-apical gradient of RWMAs was observed during HD-CONT, with higher prevalence at the apex compared to the base (p=0.03). This gradient was abolished during HD-EX, suggesting greater apical cardioprotection. Pre-treatment of cardiomyocytes with ultrafiltrates from HD-EX improved fractional shortening, Ca2+ handlings and SCaW following A/R compared to cells pre-treated with ultrafiltrates from HD-CONT.

Conclusions: IDE limits HD-induced RWMAs, and circulating humoral factors may contribute to this cardioprotection. IDE-induced benefits on RWMAs were greater at the apex. Further studies are needed to elucidate the mechanisms underlying the heterogeneous benefits of IDE on regional myocardial function.

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