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出生时无症状先天性巨细胞病毒感染的儿童的神经发育结局如何?系统文献复习。

What are the neurodevelopmental outcomes of children with asymptomatic congenital cytomegalovirus infection at birth? A systematic literature review.

机构信息

Institute for Global Health, University College London, London, UK.

St George's University Hospitals NHS Foundation Trust, London, UK.

出版信息

Rev Med Virol. 2024 Jul;34(4):e2555. doi: 10.1002/rmv.2555.

Abstract

Congenital cytomegalovirus (cCMV) is among the most common congenital infections globally. Of 85%-90% cCMV-infected infants without symptoms at birth, 10%-15% develop sequelae, most commonly sensorineural hearing loss (SNHL); their childhood neurodevelopmental outcomes are less well understood. Embase and MEDLINE were searched for publications from 16 September 2016 to 9th February 2024 to identify studies reporting primary data on neurodevelopmental outcomes in children with asymptomatic cCMV (AcCMV), measured using assessment tools or as evaluated by the study investigators, clinicians, educators, or parents. The Newcastle-Ottawa scale was applied to studies to assess risk of bias. Of 28 studies from 18 mostly high-income countries, there were 5-109 children with AcCMV per study and 6/28 had a mean or median age at last follow-up of ≥5 years. Children with AcCMV had better neurodevelopmental outcomes than children with symptomatic cCMV in 16/19 studies. Of 9/28 studies comparing AcCMV with CMV-uninfected children, six reported similar outcomes whilst three reported differences limited to measures of full-scale intelligence and receptive vocabulary among children with AcCMV and SNHL, or more generally in motor impairment. Common limitations of studies for our question were a lack of cCMV-uninfected controls, heterogeneous definitions of AcCMV, lack of focus on neurodevelopment, selection bias and inadequate follow-up. There was little evidence of children with AcCMV having worse neurodevelopmental outcomes than CMV-uninfected children, but this conclusion is limited by study characteristics and quality; findings highlight the need for well-designed and standardised approaches to investigate long-term sequelae.

摘要

先天性巨细胞病毒 (cCMV) 是全球最常见的先天性感染之一。在出生时无症状但感染了 cCMV 的 85%-90%婴儿中,有 10%-15%会出现后遗症,最常见的是感觉神经性听力损失 (SNHL);他们的儿童神经发育结局则不太为人所知。从 2016 年 9 月 16 日到 2024 年 2 月 9 日,在 Embase 和 MEDLINE 上搜索了发表关于无症状先天性巨细胞病毒感染(AcCMV)儿童神经发育结局的原始数据的出版物,这些数据是使用评估工具或由研究调查人员、临床医生、教育工作者或家长评估得出的。应用纽卡斯尔-渥太华量表对研究进行了评估,以确定其偏倚风险。在来自 18 个高收入国家的 28 项研究中,每项研究中患有 AcCMV 的儿童有 5-109 例,其中 6/28 项研究的最后一次随访的平均或中位年龄≥5 岁。在 16/19 项研究中,患有 AcCMV 的儿童的神经发育结局要好于患有有症状 cCMV 的儿童。在 9/28 项比较 AcCMV 与未感染 CMV 的儿童的研究中,有 6 项报告了相似的结果,而有 3 项报告的差异仅局限于 AcCMV 和 SNHL 儿童的全量表智力和接受性词汇量的测量,或者更普遍地局限于运动障碍的测量。针对我们的问题,研究的常见局限性包括缺乏未感染 cCMV 的对照组、AcCMV 定义不统一、缺乏对神经发育的关注、选择偏倚和随访不充分。几乎没有证据表明患有 AcCMV 的儿童的神经发育结局比未感染 CMV 的儿童差,但这一结论受到研究特征和质量的限制;研究结果突出了需要采用精心设计和标准化的方法来调查长期后遗症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/11262424/2d9c02ffeb88/RMV-34-e2555-g002.jpg

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