Accioli Riccardo, Lazzerini Pietro Enea, Salvini Viola, Cartocci Alessandra, Verrengia Decoroso, Marzotti Tommaso, Salvadori Fabio, Bisogno Stefania, Cevenini Gabriele, Voglino Michele, Gallo Severino, Pacini Sabrina, Pazzaglia Martina, Tansini Angelica, Otranto Ambra, Laghi-Pasini Franco, Acampa Maurizio, Boutjdir Mohamed, Capecchi Pier Leopoldo
Department of Medical Sciences, Surgery and Neurosciences University of Siena Siena Italy.
Division of Internal Medicine and Geriatrics, Electroimmununology Unit University Hospital of Siena Siena Italy.
J Arrhythm. 2024 Jul 31;40(5):1137-1148. doi: 10.1002/joa3.13114. eCollection 2024 Oct.
Severely ill patients with coronavirus disease 2019 (COVID-19) show an increased risk of new-onset atrioventricular blocks (AVBs), associated with high rates of short-term mortality. Recent data suggest that the uncontrolled inflammatory activation observed in these patients, specifically interleukin (IL)-6 elevation, may play an important pathogenic role by directly affecting cardiac electrophysiology. The aim of our study was to assess the acute impact of IL-6 changes on electrocardiographic indices of atrioventricular conduction in severe COVID-19.
We investigated (1) the behavior of PR-interval and PR-segment in patients with severe COVID-19 during active phase and recovery, and (2) their association with circulating IL-6 levels over time.
During active disease, COVID-19 patients showed a significant increase of PR-interval and PR-segment. Such atrioventricular delay was transient as these parameters rapidly normalized during recovery. PR-indices significantly correlated with circulating IL-6 levels over time. All these changes and correlations persisted also in the absence of laboratory signs of cardiac strain/injury or concomitant treatment with PR-prolonging drugs, repurposed or not.
Our study provides evidence that in patients with severe COVID-19 and high-grade systemic inflammation, IL-6 elevation is associated with a significant delay of atrioventricular conduction, independent of concomitant confounding factors. While transient, such alterations may enhance the risk of severe AVB and associated short-term mortality. Our data provide further support to current anti-inflammatory strategies for severe COVID-19, including IL-6 antagonists.
2019年冠状病毒病(COVID-19)重症患者新发房室传导阻滞(AVB)的风险增加,且短期死亡率较高。近期数据表明,在这些患者中观察到的不受控制的炎症激活,特别是白细胞介素(IL)-6升高,可能通过直接影响心脏电生理发挥重要的致病作用。我们研究的目的是评估IL-6变化对重症COVID-19患者房室传导心电图指标的急性影响。
我们调查了(1)重症COVID-19患者在急性期和恢复期PR间期和PR段的变化情况,以及(2)它们随时间与循环IL-6水平的关联。
在疾病活动期,COVID-19患者的PR间期和PR段显著增加。这种房室延迟是短暂的,因为这些参数在恢复过程中迅速恢复正常。PR指标随时间与循环IL-6水平显著相关。所有这些变化和相关性在没有心脏应变/损伤的实验室迹象或未使用或已重新利用的延长PR药物治疗的情况下也持续存在。
我们的研究提供了证据,表明在重症COVID-19和高度全身炎症患者中,IL-6升高与房室传导显著延迟相关,且独立于伴随的混杂因素。虽然这种改变是短暂的,但可能会增加严重AVB及相关短期死亡率的风险。我们的数据为当前针对重症COVID-19的抗炎策略,包括IL-6拮抗剂,提供了进一步支持。