Relationship between gH genotyping and clinical characteristics of children with congenital cytomegalovirus infection
10.3760/cma.j.issn.0578-1310.2019.08.005
- VernacularTitle: 先天性巨细胞病毒感染gH基因分型与临床特征的关系
- Author:
Luyan CHEN
1
;
Wei LI
1
;
Jialu XU
2
;
Ran TAO
1
;
Huamei LI
1
;
Lifang LIU
1
;
Shiqiang SHANG
1
Author Information
1. Laboratory Center, the Children′s Hospital, Zhejiang University School of Medicine, Hangzhou 310052, China
2. Department of Neurology, the Children′s Hospital, Zhejiang University School of Medicine, Hangzhou 310052, China
- Publication Type:Journal Article
- Keywords:
Cytomegalovirus infections;
Infant, newborn;
Envelope glycoprotein
- From:
Chinese Journal of Pediatrics
2019;57(8):597-602
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To study the relationship between human cytomegalovirus (HCMV) envelope glycoprotein gene H and clinical features of children with congenital cytomegalovirus infection.
Methods:A cohort study was conducted. Newborns diagnosed with congenital cytomegalovirus infection, hospitalized in the Department of Neonatology and Neonatal Intensive Care Unit (NICU) of the Children′s Hospital, Zhejiang University School of Medicine, were included from July 2013 to December 2015.HCMV-DNA gH typing in urine, sputum or blood was conducted. Patients then were divided into gH1 group and gH2 group according to gH genotypes. Patients′ data during hospitalization in newborn and 3-5 years of follow-up were collected.The relationships between gH genotype and clinical manifestations, laboratory examinations, hearing loss and neurological prognosis were analyzed by chi-square test, t test and non-parametric test.
Results:A total of 21 cases were enrolled as congenital HCMV infection and followed-up for 3-5 years. Among them, 14 (67%) were gH1 type and 7 (33%) were gH2 type. No mixed infection was found. In the two groups, there were no significant differences in the ratio of males (9/14 vs. 3/7,P=0.397), or birth weight ((2 609±686) vs. (3 021±451) g, t=-1.436, P=0.167). Gestational age of gH1 group was younger than that of gH2 group (38 (29-40) vs. 39(38-40) weeks, Z=-2.18, P=0.029). Moderate to severe hearing loss detected by neonatal auditory brainstem response were found in 40 ears (20 cases). It was higher in gH1 group than that in gH2 group (4/22 vs.0/18, χ2=5.145, P=0.023). In the imaging examination of the nervous system, the Alarcon score of gH1 group was lower than that of gH2 group (0.4±0.3 vs. 1.3±1.1, t=-2.459,P=0.024).No significant statistical difference was found in the probability of motor or language development lag in gH2 group and gH1 group (4/7 vs.4/14, P=0.346).
Conclusions:Compared with gH2 infection, gH1 infection in children has a younger gestational age. The major type of hearing loss in neonatal period is gH1 infection. Children with gH2 congenital infections are more likely to suffer from nervous systems damage.
