不对称二甲基精氨酸水平在新冠病毒感染和儿童多系统炎症综合征患儿中的预后意义

Prognostic significance of asymmetric dimethyl arginine level in pediatric patients with COVID-19 infection and MIS-C.

作者信息

Sari Memduha, Akin Fatih, Yazar Abdullah, Kilic Ahmet Osman, Akcan Ozge Metin, Akkus Abdullah, Uyar Mehmet, Topcu Cemile, Genceli Mustafa

机构信息

Department of Pediatrics, Mut State Hospital, 33600, Mersin, Turkey.

Department of Pediatrics, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.

出版信息

Eur J Pediatr. 2025 Mar 12;184(4):242. doi: 10.1007/s00431-025-06079-8.

Abstract

UNLABELLED

Coronavirus disease 2019 (COVID-19) and COVID-19-related multisystem inflammatory syndrome in children (MIS-C) is known to be a life-threatening health problem worldwide. The study investigates the potential relationship between asymmetric dimethylarginine (ADMA) levels and disease severity in such conditions. We conducted an observational, prospective study between July 2021 and January 2022. The study enrolled 98 patients diagnosed with COVID-19, 21 patients diagnosed with MIS-C, and 42 healthy individuals who served as a control group. The COVID-19 patients were further categorized into three subgroups based on their level of care: outpatients, those requiring hospitalization, and those requiring intensive care. The MIS-C patients formed a distinct fourth group. COVID-19 outpatients had a median ADMA level of 8097.0 ng/L (interquartile range: 6436.06-10840.0 ng/L), while those requiring hospitalization had a higher level of 13,195.60 ng/L (11,472.4-15,862.2 ng/L). Patients in intensive care exhibited the highest median ADMA level at 19,361.4 ng/L (15,596.65-23,367.9 ng/L). MIS-C patients also had elevated ADMA levels, with a median of 15,735.50 ng/L (13,486.6-20,532.5 ng/L). Receiver operating characteristic (ROC) curve analysis revealed that an ADMA level of 6135.15 ng/L could distinguish between patients and controls with 95% sensitivity, 100% specificity, 100% positive predictive value, and 87.5% negative predictive value.

CONCLUSIONS

In conclusion, our study is the first to investigate ADMA levels in children with COVID-19 and MIS-C. We found that ADMA levels were significantly elevated in children with COVID-19 requiring intensive care and those with MIS-C, suggesting a potential role for ADMA as a biomarker of endothelial dysfunction in these populations.

WHAT IS KNOWN

• Endothelial dysfunction is a determinant of poor prognosis in various cardiovascular diseases and plays a critical role in the pathogenesis of COVID-19 and MIS-C. • Asymmetric dimethylarginine (ADMA) is a well-known biomarker of endothelial dysfunction. Elevated levels of ADMA adversely affect vascular endothelial function by reducing nitric oxide production.

WHAT IS NEW

• It is the first to show that elevated ADMA levels in children with COVID-19 and MIS-C are associated with disease severity. • ADMA has been identified as a potential biomarker that can be used to assess the prognosis of COVID-19 and MIS-C in children and to predict the severity of the disease.

摘要

未标注

2019冠状病毒病(COVID-19)及儿童COVID-19相关多系统炎症综合征(MIS-C)是全球已知的危及生命的健康问题。本研究调查了在这些情况下不对称二甲基精氨酸(ADMA)水平与疾病严重程度之间的潜在关系。我们在2021年7月至2022年1月期间进行了一项观察性前瞻性研究。该研究招募了98例确诊为COVID-19的患者、21例确诊为MIS-C的患者以及42名作为对照组的健康个体。COVID-19患者根据其护理级别进一步分为三个亚组:门诊患者、需要住院治疗的患者以及需要重症监护的患者。MIS-C患者构成了一个单独的第四组。COVID-19门诊患者的ADMA水平中位数为8097.0 ng/L(四分位间距:6436.06 - 10840.0 ng/L),而需要住院治疗的患者水平更高,为13195.60 ng/L(11472.4 - 15862.2 ng/L)。重症监护患者的ADMA水平中位数最高,为19361.4 ng/L(15596.65 - 23367.9 ng/L)。MIS-C患者的ADMA水平也有所升高,中位数为15735.50 ng/L(13486.6 - 20532.5 ng/L)。受试者工作特征(ROC)曲线分析显示,ADMA水平为6135.15 ng/L时,区分患者和对照组的灵敏度为95%、特异性为100%、阳性预测值为100%、阴性预测值为87.5%。

结论

总之,我们的研究是首个调查COVID-19和MIS-C患儿ADMA水平的研究。我们发现,需要重症监护的COVID-19患儿和MIS-C患儿的ADMA水平显著升高,这表明ADMA在这些人群中作为内皮功能障碍生物标志物具有潜在作用。

已知信息

• 内皮功能障碍是各种心血管疾病预后不良的决定因素,在COVID-19和MIS-C的发病机制中起关键作用。• 不对称二甲基精氨酸(ADMA)是一种众所周知的内皮功能障碍生物标志物。ADMA水平升高会通过减少一氧化氮生成对血管内皮功能产生不利影响。

新发现

• 首次表明COVID-19和MIS-C患儿ADMA水平升高与疾病严重程度相关。• ADMA已被确定为一种潜在生物标志物,可用于评估儿童COVID-19和MIS-C的预后并预测疾病严重程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60d8/11903618/1e331eae26b8/431_2025_6079_Fig1_HTML.jpg

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