期刊文献+

趋化因子MIG、MCP-1、IP-10在重症手足口病中的预警价值分析 被引量:4

Values of chemokines MIG,MCP-1 and IP-10 for the early warning of severe hand-foot-mouth disease
原文传递
导出
摘要 目的探讨诱导单核因子(MIG)、单核细胞趋化蛋白-1(MCP-1)、诱导蛋白-10(IP-10)的浓度变化在手足口病疾病分期和预后判断中的临床意义,以及对重症手足口病的预警价值分析。方法选择2017年1月-2019年12月153例手足口病患者,按照病情轻重程度分为轻症组64例,重症组58例,危重症组21例,另选30例健康体检儿童为对照组。采用流式微球阵列分析术(CBA)检测血清中IP-10、MCP-1、MIG的浓度。结果重症组、危重症组中MIG、MCP-1、IP-10浓度明显高于对照组(P<0.05);且重症组、危重症组MIG、MCP-1、IP-10浓度也明显高于轻症组(P<0.05);重症组与危重症组之间差异无统计学意义(P>0.05)。MCP-1轻症组高于对照组(P<0.05)。MIG、IP-10轻症组与对照组之间差异无统计学意义(P>0.05)。采用ROC曲线分析,选取MCP=451.60 pg/ml为诊断临界点,灵敏度为94.2%、特异度为65.2%,提示MCP-1对重症手足口病诊断具有较好的预测价值。结论趋化因子IP-10、MCP-1、MIG在手足口病的重症化进展中起着重要作用,其水平的变化对疾病的预后判断和治疗有一定的参考价值,MCP-1对疾病重症化的预警价值更优。 Objective To explore the clinical significances of concentration changes of chemokines monokine induced by IFN-γ(MIG),monocyte chemoattractant protein-1(MCP-1)and IFN-γinducible protein-10(IP-10)in the staging and prognosis evaluation of hand-foot-mouth disease and to analyze their values for the early warning of severe hand-foot-mouth disease.Methods A total of 153 patients diagnosed from January 2017 to December 2019 were selected and divided into three groups according to severity of the disease:mild group(n=64),severe group(n=58),critical group(n=21).Additionally,30 healthy children were enrolled as controls.The concentrations of serum IP-10,MCP-1 and MIG were detected by cytometric bead array(CBA).Results The concentrations of IP-10,MCP-1 and MIG in the severe group were significantly higher than the normal group(P<0.05);those of IP-10,MCP-1 and MIG in the severe group and critical group were much higher than the mild group(P<0.05);the differences between the severe group and the critical group had statistical significance(P<0.05).The concentration of MCP-1 in the mild group was higher than the normal group(P<0.05).There was no statistical significance on the differences between the mild group and control group in the concentrations of MIG and IP-10(P>0.05).ROC analysis showed that,sensitivity was 94.2%and specificity was 65.2%when MCP=451.60 pg/ml was set as the diagnostic threshold,suggesting that MCP-1 had statistical significance as a predictor for the diagnosis of severe hand-foot-mouth disease.Conclusion Chemokines MIG,MCP-1 and IP-10 play important roles in the progression of hand-foot-mouth disease in the final stage.Changes in MIG,MCP-1 and IP-10 concentrations can provide reference for the prognosis evaluation and treatment of such disease.MCP-1 is more helpful in the early warning of severe hand-foot-mouth disease in the final stage.
作者 郑雅萍 单小云 陈伟 ZHENG Ya-ping;SHAN Xiao-yun;CHEN Wei(Clinical Laboratory,Jinhua Central Hospital,Jinhua,Zhejiang 321000,China)
出处 《中国卫生检验杂志》 CAS 2021年第7期832-835,共4页 Chinese Journal of Health Laboratory Technology
基金 金华市科学技术局科研基金项目(2016-4-023)。
关键词 手足口病 趋化因子 IFN-γ诱导蛋白-10 单核细胞趋化蛋白-1 IFN-γ诱导单核因子 Hand-foot-mouth disease Chemokine IFN-γinducible protein-10 Monocyte chemoattractant protein-1 Monokine induced by IFN-γ
  • 相关文献

参考文献13

二级参考文献154

  • 1Chang LY. Enterovirus 71 in Taiwan. Pediatr Neonatol,2008,49 : 103-112.
  • 2Cho HK, Lee NY, Lee H. Enterovirus 71-associated hand, foot and mouth diseases with neurologic symptoms, a university hospital experience in Korea, 2009. Korean J Pediatr,2010,53:639-643.
  • 3Koroleva GA, Lukashev AN, Khudiakova LV. Encephalomyelitis caused by enterovirus type 71 in children. Vopr Virusol,2010,55 : 4-10.
  • 4Chang LY, Lee CY, Kao CL. Hand, foot and mouth disease complicated with central nervous system involvement in Taiwan in 1950-1951 . J Formos Med Assoc,2007,106 : 173-176.
  • 5Wintergerst KA, Buckingham B, Gandrud L, et al. Association of hypoglycemia, hyperglycemia, and glucose variability with morbidity and death in the pediatric intensive care unit. Pediatrics,2006, 118 : 173-179.
  • 6Preissig CM, Rigby MR. Hyperglycaemia results from beta-cell dysfunction in critically ill children with respiratory and cardiovascular failure: a prospective observational study. Critical Care ,2009,13 : R27.
  • 7Ooi MH, Wong SC, Lewthwaite P, et al. Clinical features, diagnosis, and management of enterovirus 71 . Lancet Neurol, 2010,9:1097-1115.
  • 8Weng KF, Chen LL, Huang PN, et al. Neural pathogenesis of enterovirus 71 infection . Microbes and Infection, 2010,12 : 505- 510.
  • 9Wang SM, ki HY, Huang MC, et al. Modulation of cytokine production by intravenous immunoglobulin in patients with entemvinm 71 associated bminstem ence-phalitis. J Clin Viml, 2006,37:47-52.
  • 10Mayer SA, Lin J, Homma S, et al. Myocardial Injury and Left Ventricular Performance After Subarachnoid Hemorrhage. Stroke, 1999,30:780-786.

共引文献1409

同被引文献48

引证文献4

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部