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诊断先天性巨细胞病毒感染:不要丢弃血斑。

Diagnosing congenital Cytomegalovirus infection: don't get rid of dried blood spots.

机构信息

Department of Biomedical Sciences for Health, University of Milan, Milan, Italy.

Newborn Screening Laboratory, ASST Fatebenefratelli Sacco-PO Ospedale dei Bambini "V. Buzzi", Milan, Italy.

出版信息

BMC Infect Dis. 2020 Mar 12;20(1):217. doi: 10.1186/s12879-020-4941-z.

Abstract

BACKGROUND

Congenital Cytomegalovirus (cCMV) is a serious global public health issue that can cause irreversible fetal and neonatal congenital defects in symptomatic or asymptomatic newborns at birth. In absence of universal cCMV screening, the retrospective diagnosis of cCMV infection in children is only possible by examining Dried Blood Spot (DBS) samples routinely collected at birth and stored for different time spans depending on the newborn screening regulations in force in different countries. In this article, we summarize the arguments in favor of long-term DBS sample storage for detecting cCMV infection.

MAIN TEXT

CMV infection is the most common cause of congenital infection resulting in severe defects and anomalies that can be apparent at birth or develop in early childhood. Sensorineural hearing loss is the most frequent consequence of cCMV infection and may have a late onset and progress in the first years of life. The virological diagnosis of cCMV is essential for clinical research and public health practices. In fact, in order to assess the natural history of CMV infection and distinguish between congenital or acquired infection, children should be diagnosed early by analyzing biological samples collected in the first weeks of life (3 weeks by using viral culture and 2 weeks by molecular assays), which, unfortunately, are not always available for asymptomatic or mildly symptomatic children. It now seems possible to overcome this problem since the CMV-DNA present in the blood of congenitally infected newborns can be easily retrieved from the DBS samples on the Guthrie cards routinely collected and stored within 3 days from birth in the neonatal screening program for genetic and congenital diseases. Early collection and long-term storage are inexpensive methods for long-term bio-banking and are the key points of DBS testing for the detection of cCMV.

CONCLUSION

DBS sampling is a reliable and inexpensive method for long-term bio-banking, which enables to diagnose known infectious diseases - including cCMV - as well as diseases not jet recognized, therefore their storage sites and long-term storage conditions and durations should be the subject of political decision-making.

摘要

背景

先天性巨细胞病毒(cCMV)是一个严重的全球公共卫生问题,可导致出生时有症状或无症状的新生儿出现不可逆转的胎儿和新生儿先天性缺陷。在没有普遍进行 cCMV 筛查的情况下,只能通过检查在不同国家根据新生儿筛查法规常规收集并在不同时间段储存的干血斑(DBS)样本,来对儿童的 cCMV 感染进行回顾性诊断。在本文中,我们总结了支持长期储存 DBS 样本以检测 cCMV 感染的论点。

正文

CMV 感染是导致严重缺陷和畸形的最常见先天性感染原因,这些缺陷和畸形可能在出生时就表现出来,也可能在儿童早期发展。先天性巨细胞病毒感染的最常见后果是感音神经性听力损失,并且可能在生命的最初几年发病和进展。CMV 的病毒学诊断对于临床研究和公共卫生实践至关重要。事实上,为了评估 CMV 感染的自然史并区分先天性或后天性感染,应通过分析在生命最初几周收集的生物样本(使用病毒培养物可在 3 周内,使用分子检测可在 2 周内)来尽早诊断儿童,遗憾的是,对于无症状或症状轻微的儿童,并不总是能够获得这些样本。现在看来,这个问题可能已经得到解决,因为从出生后 3 天内常规在新生儿遗传和先天性疾病筛查计划中收集和储存的 Guthrie 卡上的 DBS 样本中,可以轻松获取先天性感染新生儿血液中的 CMV-DNA。早期采集和长期储存是进行长期生物存储的廉价方法,也是 DBS 检测用于检测 cCMV 的关键。

结论

DBS 采样是一种可靠且廉价的长期生物存储方法,它可用于诊断已知传染病(包括 cCMV)以及尚未认识到的疾病,因此,应将其存储位置、长期存储条件和持续时间作为政治决策的主题。

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