Fiedler Lukas, Motloch Lukas J, Jirak Peter, Gumerov Ruslan, Davtyan Paruir, Gareeva Diana, Lakman Irina, Tataurov Alexandr, Lasinova Gulnaz, Pavlov Valentin, Hauptmann Laurenz, Kopp Kristen, Hoppe Uta C, Lichtenauer Michael, Pistulli Rudin, Dieplinger Anna-Maria, Zagidullin Naufal
University Clinic for Internal Medicine II, Paracelsus Medical University, 5020 Salzburg, Austria.
Department of Internal Medicine, Cardiology, Nephrology and Intensive Care Medicine, Hospital Wiener Neustadt, 2700 Wiener Neustadt, Austria.
Biomedicines. 2022 Nov 10;10(11):2889. doi: 10.3390/biomedicines10112889.
Introduction: COVID-19 survivors reveal an increased long-term risk for cardiovascular disease. Biomarkers like troponins and sST-2 improve stratification of cardiovascular risk. Nevertheless, their prognostic value for identifying long-term cardiovascular risk after having survived COVID-19 has yet to be evaluated. Methods: In this single-center study, admission serum biomarkers of sST-2 and hs-TnI in a single cohort of 251 hospitalized COVID-19 survivors were evaluated. Concentrations were correlated with major cardiovascular events (MACE) defined as cardiovascular death and/or need for cardiovascular hospitalization during follow-up after hospital discharge [FU: 415 days (403; 422)]. Results: MACE was a frequent finding during FU with an incidence of 8.4% (cardiovascular death: 2.8% and/or need for cardiovascular hospitalization: 7.2%). Both biomarkers were reliable indicators of MACE (hs-TnI: sensitivity = 66.7% & specificity = 65.7%; sST-2: sensitivity = 33.3% & specificity = 97.4%). This was confirmed in a multivariate proportional-hazards analysis: besides age (HR = 1.047, 95% CI = 1.012−1.084, p = 0.009), hs-TnI (HR = 4.940, 95% CI = 1.904−12.816, p = 0.001) and sST-2 (HR = 10.901, 95% CI = 4.509−29.271, p < 0.001) were strong predictors of MACE. The predictive value of the model was further improved by combining both biomarkers with the factor age (concordance index hs-TnI + sST2 + age = 0.812). Conclusion: During long-term FU, hospitalized COVID-19 survivors, hs-TnI and sST-2 at admission, were strong predictors of MACE, indicating both proteins to be involved in post-acute sequelae of COVID-19.
新冠病毒病(COVID-19)幸存者显示出心血管疾病的长期风险增加。肌钙蛋白和可溶性生长刺激表达基因2(sST-2)等生物标志物可改善心血管风险分层。然而,它们在识别COVID-19康复后的长期心血管风险方面的预后价值尚未得到评估。方法:在这项单中心研究中,对251名住院COVID-19幸存者的单队列中入院时的血清sST-2和高敏肌钙蛋白I(hs-TnI)生物标志物进行了评估。浓度与主要心血管事件(MACE)相关,MACE定义为出院后随访期间的心血管死亡和/或心血管住院需求[随访:415天(403;422)]。结果:随访期间MACE很常见,发生率为8.4%(心血管死亡:2.8%和/或心血管住院需求:7.2%)。两种生物标志物都是MACE的可靠指标(hs-TnI:敏感性 = 66.7%,特异性 = 65.7%;sST-2:敏感性 = 33.3%,特异性 = 97.4%)。这在多变量比例风险分析中得到证实:除年龄外(风险比[HR] = 1.047,95%置信区间[CI] = 1.012−1.084,p = 0.009),hs-TnI(HR = 4.940,95% CI = 1.904−12.816,p = 0.001)和sST-2(HR = 10.901,95% CI = 4.509−29.271,p < 0.001)是MACE的强预测因子。通过将两种生物标志物与年龄因素相结合,模型的预测价值进一步提高(hs-TnI + sST2 + 年龄的一致性指数 = 0.812)。结论:在长期随访期间,住院COVID-19幸存者入院时的hs-TnI和sST-2是MACE的强预测因子,表明这两种蛋白质都参与了COVID-19的急性后遗症。