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有症状先天性巨细胞病毒感染的预后标志物

Prognostic markers of symptomatic congenital cytomegalovirus infection.

作者信息

Romanelli Roberta Maia de Castro, Magny Jean François, Jacquemard François

机构信息

Clinical Hospital, Federal Univerisity of Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

Braz J Infect Dis. 2008 Feb;12(1):38-43. doi: 10.1590/s1413-86702008000100009.

Abstract

The objective of this research was to identify maternal and fetal characteristics as prognostic markers of congenital cytomegalovirus (CMV) infection. This is a descriptive study of 13 cases of congenital CMV infection referred to Institute de Puericulture et Perinatologie de Paris (IPP) from January 2005 to October 2006. Amniotic fluid puncture was performed to research CMV polimerase chain reaction (PCR). Cordocentesis and cord blood samples at delivery were also analyzed to determinate fetal platelets count, GGT, ASAT, ALAT, CMV-DNA and IgM antibody. Variables of symptomatic and asymptomatic infants were then compared. Data were analyzed by SPSS--15.0. Mean gestational age of amniocentesis was 24.6 weeks and there was no difference of mean viral load in amniotic fluid considering infant features. Mean gestational age of cordocentesis was 26.1 weeks. There were no statistical differences of fetal viral load, IgM, platelets, GGT, ASAT and ALAT analyzed at cordocentesis samples, but at delivery, mean values of IgM and ASAT of fetal blood were increased in symptomatic ones (p= 0.03 for both parameters). When considering groups with normal and abnormal parameters, ASAT of cordon samples was also increased in symptomatic infants (p= 0.02). Sensibility, specificity, positive and negative predictive value of fetal ultrasound anomalies to detect symptomatic infants were, respectively, 80%, 62.5%, 57.1% and 83.3%. Thus, identification of markers of CMV symptomatic infants should be aimed. Prenatal diagnosis, identification and follow up of congenital CMV infected infants are important to consider treatment for symptomatic infants, trying to avoid or reducing some possible sequels.

摘要

本研究的目的是确定母体和胎儿特征作为先天性巨细胞病毒(CMV)感染的预后标志物。这是一项描述性研究,对2005年1月至2006年10月转诊至巴黎产科学与围产医学研究所(IPP)的13例先天性CMV感染病例进行了研究。进行羊水穿刺以检测CMV聚合酶链反应(PCR)。还对脐血穿刺和分娩时的脐血样本进行分析,以确定胎儿血小板计数、γ-谷氨酰转移酶(GGT)、谷草转氨酶(ASAT)、谷丙转氨酶(ALAT)、CMV-DNA和IgM抗体。然后比较有症状和无症状婴儿的变量。数据采用SPSS 15.0进行分析。羊水穿刺时的平均孕周为24.6周,考虑婴儿特征时羊水平均病毒载量无差异。脐血穿刺时的平均孕周为26.1周。脐血穿刺样本分析的胎儿病毒载量、IgM、血小板、GGT、ASAT和ALAT无统计学差异,但在分娩时,有症状婴儿的胎儿血液中IgM和ASAT的平均值升高(两个参数的p值均为0.03)。当考虑参数正常和异常的组时,有症状婴儿的脐血样本中ASAT也升高(p = 0.02)。胎儿超声异常检测有症状婴儿的敏感性、特异性、阳性和阴性预测值分别为80%、62.5%、57.1%和83.3%。因此,应致力于识别CMV有症状婴儿的标志物。先天性CMV感染婴儿的产前诊断、识别和随访对于考虑对有症状婴儿进行治疗、试图避免或减少一些可能的后遗症非常重要。

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