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2019 年冠状病毒病患者的心血管疾病:临床特征及其对心脏生物标志物评估的影响。

Coronavirus disease 2019 in patients with cardiovascular disease: clinical features and implications on cardiac biomarkers assessment.

机构信息

Covid-Cardiology Unit, Madre Giuseppina Vannini Hospital.

Internal Medicine Unit.

出版信息

J Cardiovasc Med (Hagerstown). 2021 Nov 1;22(11):832-839. doi: 10.2459/JCM.0000000000001252.

Abstract

INTRODUCTION

Previous cardiovascular disease (CVD) and myocardial involvement are common in coronavirus disease-19 (COVID-19). We investigated relationships between CVD, cardiac biomarkers and outcome in COVID-19.

METHODS

We analyzed n = 252 patients from a multicenter study and provided comparison according to the presence or absence of underlying CVD. Cardiac biomarkers high-sensitivity Troponin [upper reference of normality (URN) 35 pg/ml for Troponin I and 14 pg/ml for Troponin T] and natriuretic peptides (Nt-pro-B-type natriuretic peptide, URN 300 pg/ml and B-type natriuretic peptide, URN 100 pg/ml) were both available in n = 136.

RESULTS

Mean age was 69 ± 16 years (56% men, 31% with previous CVD). Raised hs-Troponin and natriuretic peptides were detected in 36 and 50% of the cases respectively. Age, chronic obstructive pulmonary disease, hemoglobin, hs-Troponin and natriuretic peptides were independently associated with underlying CVD (P < 0.05 for all). Compared with the normal biomarkers subgroups, patients with isolated hs-Troponin elevation had higher in-hospital mortality (31 vs. 4%, P < 0.05), similar CVD prevalence (15 vs. 11%) and trend towards higher D-dimer (930 vs. 397 ng/ml, P = 0.140). Patients with both biomarkers elevated had higher age, D-dimer, CVD and in-hospital mortality prevalence compared with other subgroups (all P < 0.05 for trend). Outcome analysis revealed previous CVD [model 1: OR 2.72 (95% CI 1.14-6.49), P = 0.024. model 2: OR 2.65 (95% CI 1.05-6.71), P = 0.039], hs-Troponin (log10) [OR 2.61 (95% CI 1.21-5.66), P = 0.015] and natriuretic peptides (log10) [OR 5.84 (95%CI 2.43-14), P < 0.001] to be independently associated with in-hospital mortality.

CONCLUSION

In our population, previous CVD was part of a vulnerable phenotype including older age, comorbidities, increased cardiac biomarkers and worse prognosis. Patients with isolated increase in hs-Troponin suffered higher mortality rates despite low prevalence of CVD, possibly explained by higher COVID-19-related systemic involvement.

摘要

简介

先前的心血管疾病(CVD)和心肌受累在冠状病毒病-19(COVID-19)中很常见。我们研究了 CVD、心脏生物标志物与 COVID-19 结局之间的关系。

方法

我们分析了来自多中心研究的 252 名患者,并根据是否存在潜在 CVD 进行了比较。心脏生物标志物高敏肌钙蛋白[正常值上限(URN)为 Troponin I 35 pg/ml 和 Troponin T 14 pg/ml]和利钠肽(Nt-pro-B 型利钠肽,URN 300 pg/ml 和 B 型利钠肽,URN 100 pg/ml)均在 n = 136 例中可用。

结果

平均年龄为 69 ± 16 岁(56%为男性,31%有先前的 CVD)。分别有 36%和 50%的病例出现 hs-Troponin 和利钠肽升高。年龄、慢性阻塞性肺疾病、血红蛋白、hs-Troponin 和利钠肽均与潜在 CVD 独立相关(所有 P 值均<0.05)。与正常生物标志物亚组相比,仅 hs-Troponin 升高的患者住院死亡率更高(31% vs. 4%,P<0.05),CVD 患病率相似(15% vs. 11%),D-二聚体呈升高趋势(930 vs. 397 ng/ml,P=0.140)。与其他亚组相比,hs-Troponin 和利钠肽均升高的患者年龄更大,D-二聚体、CVD 和住院死亡率更高(所有 P 值均<0.05)。预后分析显示,先前的 CVD [模型 1:OR 2.72(95%CI 1.14-6.49),P=0.024. 模型 2:OR 2.65(95%CI 1.05-6.71),P=0.039]、hs-Troponin(log10)[OR 2.61(95%CI 1.21-5.66),P=0.015]和利钠肽(log10)[OR 5.84(95%CI 2.43-14),P<0.001]与住院死亡率独立相关。

结论

在我们的人群中,先前的 CVD 是一种脆弱表型的一部分,包括年龄较大、合并症、心脏生物标志物增加和预后较差。尽管 CVD 患病率较低,但仅 hs-Troponin 升高的患者死亡率更高,这可能是由于 COVID-19 相关的全身受累更高。

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