International Medicine and Health Guidance News ›› 2022, Vol. 28 ›› Issue (18): 2549-2552.DOI: 10.3760/cma.j.issn.1007-1245.2022.18.007

• Scientific Research • Previous Articles     Next Articles

Changes and clinical significance of serum BNP, PCT, and IL-6 in infants with Kawasaki disease aged 0-6 months

Gu Huiru   

  1. Department of Small Infants, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, China
  • Received:2022-02-17 Online:2022-09-15 Published:2022-10-11
  • Contact: Email: huiru2012@126.com
  • Supported by:

     Joint Development Project of Henan Province Medical Science and Technology Plan in 2022 (LHGJ20220741);

     Joint Development Project of Henan Province Medical Science and Technology Plan in 2019 (LHGJ20190905)

0~6月龄婴儿川崎病血清BNP、PCT、IL-6的变化及临床意义

谷惠茹   

  1. 郑州大学附属儿童医院小婴儿科,郑州 450000
  • 通讯作者: Email:huiru2012@126.com
  • 基金资助:

    2022年河南省医学科技攻关联合共建项目(LHGJ20220741);

    2019年度河南省医学科技攻关计划联合共建项目(LHGJ20190905)

Abstract: Objective To study the expression levels of N-terminal B-type brain natriuretic peptide (NT-proBNP), procalcitonin (PCT), and interleukin-6 (IL-6) in serum of 0-6 months old infants with Kawasaki disease (KD) and their clinical significance. Methods A total of 72 children with KD hospitalized in Children's Hospital Affiliated to Zhengzhou University from January 1, 2018 to December 31, 2020 were selected and were divided into a typical group (32 cases) and an atypical group (40 cases) according to the clinical manifestations and signs. And 30 non-KD children hospitalized with fever during the same period were selected as a control group. The level of NT-proBNP in serum was determined by electrochemiluminescence method, the level of PCT in serum was determined by immunofluorescence quantitative method, and the level of IL-6 in serum was determined by enzyme-linked immunosorbent assay. The changes of NT-proBNP, IL-6, and PCT in KD children were observed after intravenous injection of human gamma globulin. χ2 test, one-way analysis of variance, Mann-Whitney U test, and Kruskal-Wallis H test were used. Results The level of serum NT-proBNP in the control group was 537.25 (392.39, 724.95) pg/ml, which was lower than those in the typical group and the atypical group [1 340.00 (924.50, 3 050.00) pg/ml and 927.90 (585.50, 1 499.50) pg/ml], with statistically significant differences (both P<0.05), but there was no statistically significant difference between the typical group and the atypical group (P>0.05). The level of serum IL-6 in the control group was 24.90 (14.75, 33.13) pg/ml, which was lower than those in the typical group and the atypical group [98.07 (83.56, 151.15) pg/ml and 72.28 (55.35, 114.30) pg/ml], with statistically significant differences (both P<0.05), but there was no statistically significant difference between the typical group and the atypical group (P>0.05). There were statistically significant differences in the PCT level among the control group [0.96 (0.55, 2.13) μg/L], the atypical group [(0.24 (0.14, 0.50) μg/L], and the typical group [0.40 (0.29, 0.74) μg/L], with statistically significant differences (all P<0.05). After treatment, the levels of NT-proBNP and IL-6 in children with KD decreased compared with those before treatment [365.10 (205.73, 736.35) pg/ml vs. 1 168.50 (773.95, 1 972.25) pg/ml, 15.55 (5.83, 46.32) pg/ml vs. 91.70 (69.24, 136.67) pg/ml], with statistically significant differences (both P<0.05). There was no statistically significant difference in the level of PCT between before and after treatment [0.12 (0.07, 0.25) μg/L vs. 0.33 (0.17, 0.58) μg/L] (P>0.05). Conclusion NT-proBNP, IL-6, and PCT can be used as important reference indexes for the diagnosis of KD in infants aged 0-6 months in the early stage of the disease.

Key words: N-terminal brain natriuretic peptide precursor, Interleukin-6, Procalcitonin, Kawasaki disease

摘要: 目的 研究0~6月龄婴儿川崎病(Kawasaki disease,KD)血清中N末端B型脑钠肽原(NT-proBNP)、降钙素原(PCT)、白细胞介素-6(IL-6)表达水平及临床意义。方法 收集2018年1月1日至2020年12月31日郑州大学附属儿童医院收治KD患儿72例,根据临床表现及体征分为典型组(32例)和不典型组(40例),并选取同期因发热住院治疗非KD患儿为对照组(30例)。典型组患儿男20例,女12例,月龄(2.7±0.2)个月;不典型组患儿男23例,女17例,月龄(2.9±0.1)个月;对照组患儿男17例,女13例,月龄(2.9±0.3)个月。应用电化学发光法检测血清中NT-proBNP水平,应用免疫荧光定量法检测血清中PCT水平,应用酶联免疫吸附法检测血清中IL-6水平。KD患儿使用静注人丙种球蛋白后比较NT-proBNP、IL-6、PCT的变化。采用χ2检验、单因素方差分析、Mann-Whitney U检验、Kruskal-wallis H检验。结果 对照组患儿血清NT-proBNP水平537.25(392.39,724.95)pg/ml低于典型组1 340.00(924.50,3 050.00)pg/ml和不典型组927.90(585.50,1 499.50)pg/ml,差异均有统计学意义(均P<0.05),典型组和不典型组相比差异无统计学意义(P>0.05)。对照组患儿血清IL-6水平24.90(14.75,33.13)pg/ml低于典型组98.07(83.56,151.15)pg/ml和不典型组72.28(55.35,114.30)pg/ml,差异均有统计学意义(均P<0.05),典型组和不典型组相比差异无统计学意义(P>0.05)。对照组患儿PCT水平0.96(0.55,2.13)μg/L与不典型组0.24(0.14,0.50)μg/L、典型组0.40(0.29,0.74)μg/L比较,差异均有统计学意义(均P<0.05)。治疗后KD患儿NT-proBNP、IL-6水平较治疗前NT-proBNP、IL-6下降[365.10(205.73,736.35)pg/ml比1 168.50(773.95,1 972.25)pg/ml,15.55(5.83,46.32)pg/ml比91.70(69.24,136.67)pg/ml],差异均有统计学意义(均P<0.05);治疗后患儿PCT水平与治疗前比较差异无统计学意义[0.12(0.07,0.25)μg/L比0.33(0.17,0.58)μg/L](P>0.05)。结论 NT-proBNP、IL-6、PCT疾病前期联合检测可作为辅助诊断0~6月龄小婴儿KD的重要参考指标。

关键词: N末端脑钠肽前体, 白细胞介素-6, 降钙素原, 川崎病