Cytomegalovirus (CMV) Saliva Shedding Kinetics in Children with Congenital CMV Infection (cCMV).

IF 2.5 4区 医学 Q3 INFECTIOUS DISEASES
Swetha Pinninti, Sunil Pati, Zdenek Novak, Karen Fowler, Suresh Boppana, Shannon Ross
{"title":"Cytomegalovirus (CMV) Saliva Shedding Kinetics in Children with Congenital CMV Infection (cCMV).","authors":"Swetha Pinninti, Sunil Pati, Zdenek Novak, Karen Fowler, Suresh Boppana, Shannon Ross","doi":"10.1093/jpids/piaf040","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Congenital CMV (cCMV) is a common congenital viral infection worldwide and the most common cause of childhood non-genetic sensorineural hearing loss (SNHL). The kinetics of CMV detection (shedding) from mucosal surfaces have not been extensively described in children with cCMV due to a lack of systematic newborn CMV screening and follow-up protocols. The aim of this study is to describe the natural history of saliva CMV shedding in a cCMV cohort, which was identified through universal newborn screening.</p><p><strong>Methods: </strong>As part of the CMV and Hearing Multicenter Screening study (CHIMES), 100,332 newborns were screened, and those confirmed to have cCMV were followed prospectively every six months for four years to determine hearing outcomes. Saliva CMV DNA shedding kinetics, including duration, viral load (VL), and intermittent shedding are described and compared between groups with and without newborn symptoms and hearing loss in children with ≥ 5 visits.</p><p><strong>Results: </strong>The 197 children with confirmed cCMV shed CMV DNA in saliva for a median of 20 months with CMV shedding frequency decreasing from 100% at cCMV confirmation to 9.5% four years after enrollment. Similarly, median CMV DNA VL levels decreased from 8.89X106 IU/ml at the confirmation visit to 1.64X103 IU/ml at the 4-year follow-up visit. Saliva CMV shedding duration was similar between children with or without newborn symptoms (median 20 months for both groups; p = 0.57) or between those with SNHL vs normal hearing (p = 0.8). A third of the cohort intermittently shed CMV DNA in saliva (64/197, 32.5%).</p><p><strong>Conclusions: </strong>In this large cohort of children with cCMV identified by universal CMV newborn screening, CMV DNA was detectable in saliva for a median of 20 months, irrespective of newborn symptoms or hearing outcomes. Intermittent shedding was noted in a third of the cohort.</p>","PeriodicalId":17374,"journal":{"name":"Journal of the Pediatric Infectious Diseases Society","volume":" ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Pediatric Infectious Diseases Society","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/jpids/piaf040","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Congenital CMV (cCMV) is a common congenital viral infection worldwide and the most common cause of childhood non-genetic sensorineural hearing loss (SNHL). The kinetics of CMV detection (shedding) from mucosal surfaces have not been extensively described in children with cCMV due to a lack of systematic newborn CMV screening and follow-up protocols. The aim of this study is to describe the natural history of saliva CMV shedding in a cCMV cohort, which was identified through universal newborn screening.

Methods: As part of the CMV and Hearing Multicenter Screening study (CHIMES), 100,332 newborns were screened, and those confirmed to have cCMV were followed prospectively every six months for four years to determine hearing outcomes. Saliva CMV DNA shedding kinetics, including duration, viral load (VL), and intermittent shedding are described and compared between groups with and without newborn symptoms and hearing loss in children with ≥ 5 visits.

Results: The 197 children with confirmed cCMV shed CMV DNA in saliva for a median of 20 months with CMV shedding frequency decreasing from 100% at cCMV confirmation to 9.5% four years after enrollment. Similarly, median CMV DNA VL levels decreased from 8.89X106 IU/ml at the confirmation visit to 1.64X103 IU/ml at the 4-year follow-up visit. Saliva CMV shedding duration was similar between children with or without newborn symptoms (median 20 months for both groups; p = 0.57) or between those with SNHL vs normal hearing (p = 0.8). A third of the cohort intermittently shed CMV DNA in saliva (64/197, 32.5%).

Conclusions: In this large cohort of children with cCMV identified by universal CMV newborn screening, CMV DNA was detectable in saliva for a median of 20 months, irrespective of newborn symptoms or hearing outcomes. Intermittent shedding was noted in a third of the cohort.

巨细胞病毒(CMV)先天性巨细胞病毒感染(cCMV)儿童唾液脱落动力学。
背景:先天性巨细胞病毒(cCMV)是一种常见的先天性病毒感染,是儿童非遗传性感音神经性听力损失(SNHL)的最常见原因。由于缺乏系统的新生儿巨细胞病毒筛查和随访方案,cCMV患儿粘膜表面巨细胞病毒检测(脱落)的动力学尚未得到广泛的描述。本研究的目的是描述cCMV队列中唾液CMV脱落的自然历史,这是通过普遍的新生儿筛查确定的。方法:作为CMV和听力多中心筛查研究(CHIMES)的一部分,对100,332名新生儿进行了筛查,并对确认患有cCMV的新生儿每6个月进行前瞻性随访,为期4年,以确定听力结局。描述了唾液CMV DNA脱落动力学,包括持续时间、病毒载量(VL)和间歇性脱落,并比较了有和没有新生儿症状和就诊≥5次的儿童听力损失组之间的差异。结果:197例确诊为cCMV的儿童在唾液中脱落CMV DNA的时间中位数为20个月,CMV脱落频率从cCMV确诊时的100%下降到入组4年后的9.5%。同样,CMV DNA VL水平中位数从确认就诊时的8.89X106 IU/ml下降到4年随访时的1.64X103 IU/ml。有或没有新生儿症状的儿童的唾液巨细胞病毒脱落持续时间相似(两组的中位数为20个月;p = 0.57)或SNHL患者与正常听力患者之间的差异(p = 0.8)。三分之一的队列间歇性地在唾液中脱落CMV DNA(64/ 197,32.5%)。结论:在这个通过通用CMV新生儿筛查确定的cCMV儿童大队列中,无论新生儿症状或听力结果如何,唾液中检测到CMV DNA的中位时间为20个月。三分之一的人出现了间歇性脱发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of the Pediatric Infectious Diseases Society
Journal of the Pediatric Infectious Diseases Society Medicine-Pediatrics, Perinatology and Child Health
CiteScore
6.70
自引率
0.00%
发文量
179
期刊介绍: The Journal of the Pediatric Infectious Diseases Society (JPIDS), the official journal of the Pediatric Infectious Diseases Society, is dedicated to perinatal, childhood, and adolescent infectious diseases. The journal is a high-quality source of original research articles, clinical trial reports, guidelines, and topical reviews, with particular attention to the interests and needs of the global pediatric infectious diseases communities.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信