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半胱天冬酶-3和心肌肌钙蛋白I在评估儿童新冠病毒病和多系统炎症综合征心血管风险中的预后价值

Prognostic Value of Caspase-3 and Cardiac Troponin I in Assessing Cardiovascular Risk in Pediatric COVID-19 and Multisystem Inflammatory Syndrome.

作者信息

Kozak Kateryna, Pavlyshyn Halyna, Vari Sandor George

机构信息

Department of Pediatrics, No.2, I. Horbachevsky Ternopil National Medical University, Ternopil, Ukraine.

International Research and Innovation in Medicine Program, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

出版信息

J Multidiscip Healthc. 2025 May 30;18:3009-3019. doi: 10.2147/JMDH.S514776. eCollection 2025.

DOI:10.2147/JMDH.S514776
PMID:40463585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12132052/
Abstract

PURPOSE

The studies of COVID-19-related cardiovascular events in children are not widespread. Criteria for cardiovascular dysfunction have been explicitly proposed for multisystem inflammatory syndrome in children (MIS-C), while for other COVID-19 manifestations, it remains unclear. Although instrumental confirmation of cardiovascular injury is well-known, laboratory markers for such injuries have not been thoroughly studied. Our study aimed to identify prognostic cut-off values for caspase-3 and cardiac troponin I (cTI) to define cardiovascular injury in pediatric COVID-19 patients during acute infection and MIS-C.

PATIENTS AND METHODS

A cross-sectional study was conducted in Ternopil, Ukraine, involving two hundred sixty children aged one month to 17 years who had not previously been vaccinated against SARS-CoV-2. The research focused on different severities of COVID-19: mild (n=87); moderate (n=66); severe COVID-19 (n=22); MIS-C (n=40) and 45 non-SARS-CoV-2 infected persons. ELISA tests were used to measure caspase-3 and cardiac troponin I levels.

RESULTS

Caspase-3 and cTI levels were significantly higher in patients with severe COVID-19 and MIS-C compared to non-infected individuals. Furthermore, COVID-19 and MIS-C patients with cardiac abnormalities had substantially higher levels of caspase-3 and cTI compared to those without structural changes. The study also revealed a positive correlation between caspase-3 and cardiac troponin I levels in both the COVID-19 group (r = 0.41; p < 0.05) and the MIS-C group (r = 0.55; p < 0.05). The study has identified specific cut-off values for caspase-3 and cTI that can be used to predict cardiovascular structural changes in pediatric patients with COVID-19 and MIS-C. These values are caspase-3 ≥ 5.22 ng/mL, cTI≥ 1.34 ng/mL for COVID-19, and caspase-3 ≥ 6.52 ng/mL and cTI ≥ 0.39 ng/mL for MIS-C.

CONCLUSION

Current research has demonstrated that children with severe COVID-19, as well as patients with MIS-C, must undergo careful screening for cardiovascular events that could include biomarkers.

摘要

目的

关于儿童新冠病毒相关心血管事件的研究并不广泛。儿童多系统炎症综合征(MIS-C)的心血管功能障碍标准已明确提出,但对于其他新冠病毒表现,仍不清楚。尽管心血管损伤的仪器确认众所周知,但此类损伤的实验室标志物尚未得到充分研究。我们的研究旨在确定半胱天冬酶 - 3和心肌肌钙蛋白I(cTI)的预后临界值,以界定急性感染期和MIS-C期儿科新冠病毒患者的心血管损伤。

患者与方法

在乌克兰捷尔诺波尔进行了一项横断面研究,纳入260名年龄在1个月至17岁之间、此前未接种过新冠病毒疫苗的儿童。该研究聚焦于不同严重程度的新冠病毒感染:轻症(n = 87);中症(n = 66);重症新冠病毒感染(n = 22);MIS-C(n = 40)以及45名未感染新冠病毒的个体。采用酶联免疫吸附测定(ELISA)试验测量半胱天冬酶 - 3和心肌肌钙蛋白I水平。

结果

与未感染个体相比,重症新冠病毒感染和MIS-C患者的半胱天冬酶 - 3和cTI水平显著更高。此外,有心脏异常的新冠病毒感染和MIS-C患者的半胱天冬酶 - 3和cTI水平明显高于无结构变化的患者。该研究还揭示,在新冠病毒感染组(r = 0.41;p < 0.05)和MIS-C组(r = 0.55;p < 0.05)中,半胱天冬酶 - 3和心肌肌钙蛋白I水平呈正相关。该研究确定了半胱天冬酶 - 3和cTI的特定临界值可用于预测儿科新冠病毒感染和MIS-C患者的心血管结构变化。这些值对于新冠病毒感染而言,半胱天冬酶 - 3≥5.22 ng/mL,cTI≥1.34 ng/mL;对于MIS-C而言,半胱天冬酶 - 3≥6.52 ng/mL且cTI≥0.39 ng/mL。

结论

当前研究表明,重症新冠病毒感染儿童以及MIS-C患者必须接受仔细筛查,以检测可能包括生物标志物在内的心血管事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/e3ff8ee7228c/JMDH-18-3009-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/6bdf58236cf3/JMDH-18-3009-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/11d3d1eaad4f/JMDH-18-3009-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/a8134b70f0c3/JMDH-18-3009-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/e3ff8ee7228c/JMDH-18-3009-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/6bdf58236cf3/JMDH-18-3009-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/11d3d1eaad4f/JMDH-18-3009-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/a8134b70f0c3/JMDH-18-3009-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b34/12132052/e3ff8ee7228c/JMDH-18-3009-g0004.jpg

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