Determination of Serum Procalcitonin Level in Kawasaki Disease

Reihaneh Sedghi, Anahita Sanaei Dashti, Hossein Esmaeilzadeh
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Abstract

Background: The most frequent cause of coronary artery aneurysm in children is Kawasaki disease (KD). Recently, limited studies on procalcitonin (PCT) were performed to find a biomarker for the diagnosis or prognosis of children with KD. Objectives: This study aimed to compare serum PCT levels between complete and incomplete KD and testify to the predictive validity of PCT for intravenous immunoglobulin (IVIG) resistance and predicting coronary artery lesions (CALs). Methods: This cross-sectional study was conducted at Namazi hospital in Shiraz, Iran, in 2019. All KD patients admitted to the hospital were included, with parental consent obtained. Kawasaki disease patients were categorized as complete KD (cKD) or incomplete KD (iKD). Two-dimensional echocardiography was performed, and peripheral venous blood was examined for PCT levels and other markers. All patients received IVIG and aspirin as standard treatment. The presence of coronary artery abnormalities (CAAs) was determined based on coronary artery size and morphology. We used Stata software version 14.0 for data analysis. Logistic regression models identified predictive factors for coronary complications. This study determined the optimal PCT cut-off point for predicted coronary complications using receiver operating characteristic (ROC) curve analysis. Approval was obtained from the Research Ethics Committees of Shiraz University of Medical Sciences. Results: Procalcitonin values in 38 children hospitalized with acute KD ranged from 0.2 ng/mL to 10 ng/mL, with a mean of 2.65 ng/m. There was no correlation of PCT with patients’ age or gender, incomplete KD, or IVIG resistance. The serum PCT concentration was higher in patients with CAL (P = 0.009). The best PCT cut-off value for CAL prediction was 2.5 ng/mL (corresponding sensitivity = 81.8% and specificity = 68.7%), considering CAL prevalence as the studied group. Conclusions: Supplementary research is needed to determine the sensitivity and specificity of PCT for the diagnosis and prognosis of KD. Procalcitonin might be of value in predicting which children are at increased risk for CALs to intensify therapy.
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测定川崎病的血清降钙素原水平
背景:儿童冠状动脉瘤最常见的病因是川崎病(KD)。最近,有关降钙素原(PCT)的研究非常有限,目的是为 KD 儿童的诊断或预后寻找一种生物标志物。研究目的本研究旨在比较完全性和不完全性 KD 的血清 PCT 水平,并证明 PCT 对静脉注射免疫球蛋白(IVIG)耐受性和预测冠状动脉病变(CALs)的预测有效性。研究方法这项横断面研究于 2019 年在伊朗设拉子的 Namazi 医院进行。所有入院的 KD 患者均被纳入研究,并征得了家长的同意。川崎病患者被分为完全性川崎病(cKD)和不完全性川崎病(iKD)。对患者进行二维超声心动图检查,并检测外周静脉血的PCT水平和其他标志物。所有患者都接受了 IVIG 和阿司匹林的标准治疗。根据冠状动脉的大小和形态确定是否存在冠状动脉异常(CAA)。我们使用 Stata 软件 14.0 版进行数据分析。逻辑回归模型确定了冠状动脉并发症的预测因素。本研究采用接收器操作特征曲线(ROC)分析法确定了预测冠状动脉并发症的最佳 PCT 切点。研究获得了设拉子医科大学研究伦理委员会的批准。研究结果38 名急性 KD 住院患儿的降钙素原值从 0.2 纳克/毫升到 10 纳克/毫升不等,平均值为 2.65 纳克/毫升。PCT 与患者的年龄或性别、不完全 KD 或 IVIG 抗药性均无相关性。CAL 患者的血清 PCT 浓度更高(P = 0.009)。以 CAL 患病率为研究对象,预测 CAL 的最佳 PCT 临界值为 2.5 纳克/毫升(相应的敏感性 = 81.8%,特异性 = 68.7%)。结论:需要进行补充研究,以确定 PCT 对 KD 诊断和预后的敏感性和特异性。降钙素原可能有助于预测哪些儿童患 CAL 的风险较高,从而加强治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Comprehensive Pediatrics
Journal of Comprehensive Pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.90
自引率
0.00%
发文量
28
期刊介绍: Journal of Comprehensive Pediatrics is the official publication of Iranian Society of Pediatrics (ISP) and a peer-reviewed medical journal which is published quarterly. It is informative for all practicing pediatrics including general medical profession.
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