Acute alterations in blood lactate in the setting of transient stress induced myocardial ischaemia.

IF 2.8 4区 医学 Q2 PHYSIOLOGY
Jamie M O'Driscoll, Elliot Smith, Matchel Bibat, Jamie J Edwards, Claire Compton, Konstantina Kipourou, Damian Coleman, Jonathan Wiles, Eliane Cunliffe, Anna Marciniak, Rajan Sharma
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引用次数: 0

Abstract

An elevation in resting venous blood lactate ([La-]b) levels in conditions of myocardial hypoperfusion is associated with adverse prognosis and survival. This investigation aimed to assess changes in venous [La-]b levels induced by dobutamine stress in the presence and absence of myocardial ischaemia and adverse outcomes at 1 year. Four hundred and four consecutive patients (mean age 70 ± 10 years, 243 male) reporting chest pain underwent dobutamine stress echocardiography (DSE) and were categorised as ischaemic (IS) or non-ischaemic (NI) responders. Conventional and global longitudinal strain (GLS) echocardiographic measures were recorded at rest. Venous [La-]b samples were acquired at rest, peak stress and 1, 3, 5 and 10 min into recovery using a commercially available Lactate Pro 2 device. There were no significant differences in [La-]b concentrations between IS (1.75 ± 0.76 mmol L-1) and NI (1.73 ± 0.60 mmol L-1) responders at baseline (P = 0.592). However, [La-]b concentrations were significantly greater at peak stress (1.83 ± 0.57 vs. 1.68 ± 0.60 mmol L-1), 1 (1.90 ± 0.56 vs. 1.73 ± 0.71 mmol L-1), 3 (1.97 ± 0.56 vs. 1.73 ± 0.71 mmol L-1), 5 (1.98 ± 0.60 vs. 1.74 ± 0.70 mmol L-1) and 10 min (2.01 ± 0.63 vs. 1.76 ± 0.71 mmol L-1) into recovery between IS and NI responders (all P < 0.001). GLS was significantly lower in IS compared to NI (-15.5 ± 2.9 vs. -16.2% ± 2.7%, P = 0.02) responders at baseline. In patients who experienced an adverse cardiac event during 1 year of follow-up, GLS (-14.4 ± 2.7 vs. -16.1% ± 2.8%, P < 0.001) and [La-]b concentrations were significantly lower at baseline (1.54 ± 0.55 vs. 1.78 ± 0.70 mmol L-1, P = 0.02), as were [La-]b concentrations at 5 (1.68 ± 0.55 vs. 1.88 ± 0.68 mmol L-1, P = 0.04) and 10 min (1.70 ± 0.56 vs. 1.93 ± 0.71 mmol L-1, P = 0.02) into recovery compared to patients who did not experience an adverse event. GLS (hazard ration (HR) 1.21; 95% CI: 1.11-1.33, P < 0.001) and [La-]b concentrations at 10 min into recovery (HR 0.54; 95% CI: 0.33-0.85, P = 0.01) were significant independent predictors of an adverse event. Transient myocardial ischaemia is associated with a significant elevation in [La-]b concentrations, which extends into the recovery period, compared to NI responders. A blunted metabolic response to dobutamine stress and attenuated longitudinal myocardial mechanics are independently associated with short-term adverse events.

短暂应激引起心肌缺血时血乳酸的急性改变。
心肌灌注不足时静息静脉血乳酸([La-]b)水平升高与不良预后和生存相关。本研究旨在评估在心肌缺血存在和不存在的情况下,多巴酚丁胺应激引起的静脉[La-]b水平的变化以及1年后的不良结局。报告胸痛的连续404例患者(平均年龄70±10岁,243例男性)接受了多巴酚丁胺应激超声心动图(DSE)检查,并被分为缺血性(IS)或非缺血性(NI)应答者。静息时记录常规和全局纵向应变(GLS)超声心动图测量。使用市售的Lactate Pro 2装置在静置、峰值应激和恢复后1、3、5和10分钟采集静脉[La-]b样本。IS应答者(1.75±0.76 mmol L-1)与NI应答者(1.73±0.60 mmol L-1)基线时[La-]b浓度无显著差异(P = 0.592)。然而,La - b的浓度在峰值应力显著更大(1.83±0.57和1.68±0.60更易与l - 1), 1(1.90±0.56和1.73±0.71更易与l - 1)、3(1.97±0.56和1.73±0.71更易与l - 1)、5(1.98±0.60和1.74±0.70更易与l - 1)和10分钟(2.01±0.63和1.76±0.71更易与l - 1)之间复苏和倪反应(P - b]浓度都显著降低在基线(1.54±0.55和1.78±0.70更易与l - 1, P = 0.02),与未发生不良事件的患者相比,恢复后5分钟(1.68±0.55∶1.88±0.68 mmol -1, P = 0.04)和10分钟(1.70±0.56∶1.93±0.71 mmol -1, P = 0.02)的[La-]b浓度也是如此。危险比(HR) 1.21;95% CI: 1.11-1.33,恢复后10 min P -]b浓度(HR 0.54;95% CI: 0.33-0.85, P = 0.01)是不良事件的显著独立预测因子。与NI反应者相比,短暂性心肌缺血与[La-]b浓度的显著升高相关,并延续至恢复期。多巴酚丁胺应激的代谢反应迟钝和纵向心肌力学减弱与短期不良事件独立相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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