Tu Yi-Fang, Lin Chih-Hao, Lee Hsueh-Te, Yan Jing-Jou, Sze Chun-I, Chou Ya-Ping, Ho Chien-Jung, Huang Chao-Ching
Department of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, 138 Sheng-Li Road, Tainan 70403, Taiwan.
Department of Emergency Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Int J Infect Dis. 2015 May;34:105-11. doi: 10.1016/j.ijid.2015.03.017. Epub 2015 Mar 25.
Neurogenic pulmonary edema (NPE) is a fatal complication in children with enterovirus 71 (EV71) encephalitis. Endothelin 1 (ET-1), a potent vasoconstrictor, can induce pulmonary edema in rats via intrathecal injections. Thus, it was hypothesized that ET-1 in the central nervous system may correlate with NPE in children with EV71 encephalitis.
Clinical data and ET-1 in the cerebrospinal fluid (CSF) were compared between three groups: (1) EV71 encephalitis with NPE; (2) EV71 encephalitis without NPE; and (3) non-EV71 aseptic meningitis. ET-1 immunostaining was performed on the brainstem of autopsy patients.
The EV71 with NPE group showed significantly increased CSF levels of ET-1 compared to the EV71 without NPE and the non-EV71 aseptic meningitis groups (both p<0.01). The optimum cut-off point of ET-1 to predict NPE in EV71 patients, based on the receiver operating characteristic curve, was 0.5 pg/ml (sensitivity 83%, specificity 100%). Immunostaining in the brainstem showed increased ET-1 expression, mainly in the oligodendrocytes, in EV71 with NPE patients compared with control patients.
ET-1 in the central nervous system may play a role in the development of NPE in children with EV71 infection and could be used as a biomarker or therapeutic target for NPE in EV71 encephalitis.
神经源性肺水肿(NPE)是肠道病毒71型(EV71)脑炎患儿的一种致命并发症。内皮素1(ET-1)是一种强效血管收缩剂,通过鞘内注射可诱导大鼠发生肺水肿。因此,推测中枢神经系统中的ET-1可能与EV71脑炎患儿的NPE相关。
比较三组患儿的临床资料及脑脊液(CSF)中的ET-1水平:(1)伴有NPE的EV71脑炎;(2)不伴有NPE的EV71脑炎;(3)非EV71无菌性脑膜炎。对尸检患者的脑干进行ET-1免疫染色。
与不伴有NPE的EV71脑炎组和非EV71无菌性脑膜炎组相比,伴有NPE的EV71脑炎组CSF中ET-1水平显著升高(均p<0.01)。根据受试者工作特征曲线,预测EV71患者发生NPE的ET-1最佳截断点为0.5 pg/ml(敏感性83%,特异性100%)。与对照组患者相比,伴有NPE的EV71脑炎患者脑干免疫染色显示ET-1表达增加,主要在少突胶质细胞中。
中枢神经系统中的ET-1可能在EV71感染患儿NPE的发生中起作用,可作为EV71脑炎NPE的生物标志物或治疗靶点。