Liao Min-Tsun, Chen Chun-Kai, Lin Ting-Tse, Cheng Li-Ying, Ting Hung-Wen, Liu Yen-Bin
Division of Cardiology, Department of Medicine, National Taiwan University Hospital Hsinchu Branch, Hsinchu 300, Taiwan.
Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei 100, Taiwan.
J Clin Med. 2020 Nov 16;9(11):3677. doi: 10.3390/jcm9113677.
Atrial fibrillation (AF) is associated with morbidity and mortality. Modern pacemakers can detect atrial high-rate episodes (AHREs) as a surrogate for AF. It remains controversial whether inflammation is a cause or a consequence of AF. This study investigated whether the inflammatory biomarker high-sensitivity C-reactive protein (hs-CRP) can predict subsequent AHREs. This study gathered prospective data from patients with pacemakers and a left ventricle EF ≥ 50% between 2015 and 2019. The hs-CRP and other cardiac biomarkers at baseline and device-detected AHREs, defined as atrial rate ≥ 180 bpm and duration ≥ 6 min, were determined. Cox regression analysis was used to estimate the independent predictors for AHREs. A total of 171 consecutive patients were included. During the median follow-up of 614 days, 66 patients (39%) developed subsequent AHREs. In the univariate Cox regression analysis, sick sinus syndrome ( = 0.005), prior AF ( < 0.001), mitral A velocity ( = 0.008), and hs-CRP ( = 0.013) showed significant association with the increased risk of AHREs. In the multivariate Cox regression model, hs-CRP (HR = 1.121, 95% confidence interval = 1.015-1.238, = 0.024) retained its significance. Our results suggest that elevated hs-CRP could predict subsequent AHREs and that inflammation could play a role in AF pathogenesis in patients with preserved EF.
心房颤动(AF)与发病率和死亡率相关。现代起搏器可检测到心房高频率发作(AHREs)作为AF的替代指标。炎症是AF的原因还是结果仍存在争议。本研究调查了炎症生物标志物高敏C反应蛋白(hs-CRP)是否能预测随后的AHREs。本研究收集了2015年至2019年间有起搏器且左心室射血分数(EF)≥50%的患者的前瞻性数据。测定了基线时的hs-CRP和其他心脏生物标志物以及设备检测到的AHREs,AHREs定义为心房率≥180次/分钟且持续时间≥6分钟。采用Cox回归分析来估计AHREs的独立预测因素。共纳入171例连续患者。在中位随访614天期间,66例患者(39%)出现了随后的AHREs。在单变量Cox回归分析中,病态窦房结综合征(P = 0.005)、既往AF(P < 0.001)、二尖瓣A峰速度(P = 0.008)和hs-CRP(P = 0.013)与AHREs风险增加显著相关。在多变量Cox回归模型中,hs-CRP(风险比[HR] = 1.121,95%置信区间 = 1.015 - 1.238,P = 0.024)仍具有显著性。我们的结果表明,hs-CRP升高可预测随后的AHREs,并且炎症可能在EF保留的患者的AF发病机制中起作用。