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白细胞介素-6升高是新冠病毒相关心率校正QT间期延长的关键致病因素。

Interleukin-6 Elevation Is a Key Pathogenic Factor Underlying COVID-19-Associated Heart Rate-Corrected QT Interval Prolongation.

作者信息

Lazzerini Pietro Enea, Accioli Riccardo, Acampa Maurizio, Zhang Wen-Hui, Verrengia Decoroso, Cartocci Alessandra, Bacarelli Maria Romana, Xin Xiaofeng, Salvini Viola, Chen Ke-Su, Salvadori Fabio, D'errico Antonio, Bisogno Stefania, Cevenini Gabriele, Marzotti Tommaso, Capecchi Matteo, Laghi-Pasini Franco, Chen Long, Capecchi Pier Leopoldo, Boutjdir Mohamed

机构信息

Department of Medical Sciences, Surgery and Neurosciences, University of Siena, Siena, Italy.

Stroke Unit, University Hospital of Siena, Siena, Italy.

出版信息

Front Cardiovasc Med. 2022 May 19;9:893681. doi: 10.3389/fcvm.2022.893681. eCollection 2022.

Abstract

BACKGROUND

Heart rate-corrected QT interval (QTc) prolongation is prevalent in patients with severe coronavirus disease 2019 (COVID-19) and is associated with poor outcomes. Recent evidence suggests that the exaggerated host immune-inflammatory response characterizing the disease, specifically interleukin-6 (IL-6) increase, may have an important role, possibly direct effects on cardiac electrophysiology. The aim of this study was to dissect the short-term discrete impact of IL-6 elevation on QTc in patients with severe COVID-19 infection and explore the underlying mechanisms.

METHODS

We investigated the following mechanisms: (1) the QTc duration in patients with COVID-19 during the active phase and recovery, and its association with C-reactive protein (CRP) and IL-6 levels; (2) the acute impact of IL-6 administration on QTc in an guinea pig model; and (3) the electrophysiological effects of IL-6 on ventricular myocytes .

RESULTS

In patients with active severe COVID-19 and elevated IL-6 levels, regardless of acute myocardial injury/strain and concomitant QT-prolonging risk factors, QTc was significantly prolonged and rapidly normalized in correlation with IL-6 decrease. The direct administration of IL-6 in an guinea pig model acutely prolongs QTc duration. Moreover, ventricular myocytes incubated with IL-6 show evident prolongation in the action potential, along with significant inhibition in the rapid delayed rectifier potassium current (I).

CONCLUSION

For the first time, we demonstrated that in severe COVID-19, systemic inflammatory activation can promote QTc prolongation IL-6 elevation, leading to ventricular electric remodeling. Despite being transitory, such modifications may significantly contribute to arrhythmic events and associated poor outcomes in COVID-19. These findings provide a further rationale for current anti-inflammatory treatments for COVID-19, including IL-6-targeted therapies.

摘要

背景

校正心率后的QT间期(QTc)延长在重症2019冠状病毒病(COVID-19)患者中很常见,且与不良预后相关。最近的证据表明,该疾病所特有的过度的宿主免疫炎症反应,特别是白细胞介素-6(IL-6)升高,可能起重要作用,可能对心脏电生理有直接影响。本研究的目的是剖析IL-6升高对重症COVID-19感染患者QTc的短期离散影响,并探索其潜在机制。

方法

我们研究了以下机制:(1)COVID-19患者在急性期和恢复期的QTc持续时间,及其与C反应蛋白(CRP)和IL-6水平的关系;(2)在豚鼠模型中给予IL-6对QTc的急性影响;(3)IL-6对心室肌细胞的电生理作用。

结果

在活动性重症COVID-且IL-6水平升高的患者中,无论有无急性心肌损伤/劳损以及伴随的QT延长危险因素,QTc均显著延长,并随着IL-6降低而迅速恢复正常。在豚鼠模型中直接给予IL-6可急性延长QTc持续时间。此外,用IL-6孵育的心室肌细胞动作电位明显延长,同时快速延迟整流钾电流(I)受到显著抑制。

结论

我们首次证明,在重症COVID-19中,全身炎症激活可通过IL-6升高促进QTc延长,导致心室电重构。尽管这种改变是暂时的,但可能会显著促成COVID-19中的心律失常事件及相关不良预后。这些发现为目前针对COVID-19的抗炎治疗,包括靶向IL-6的疗法,提供了进一步的理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d99/9161021/dcd86a91c877/fcvm-09-893681-g001.jpg

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