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患有自闭症的儿童应考虑产前获得性巨细胞病毒感染。

Prenatal acquired cytomegalovirus infection should be considered in children with autism.

作者信息

Engman Mona-Lisa, Sundin Mikael, Miniscalco Carmela, Westerlund Joakim, Lewensohn-Fuchs Ilona, Gillberg Christopher, Fernell Elisabeth

机构信息

Division of Pediatrics, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Division of Pediatrics, Emergency and General Pediatrics Section, Astrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Acta Paediatr. 2015 Aug;104(8):792-5. doi: 10.1111/apa.13032. Epub 2015 May 14.

Abstract

AIM

The aim of the study was to evaluate the prevalence of congenital cytomegalovirus infection (CMV) in a representative sample of children with autism spectrum disorder.

METHODS

In a representative group of 115 preschool children with autism spectrum disorder, of whom 33 also had intellectual disability, the dried blood spots from the newborn metabolic screening were analysed for CMV DNA using TaqMan polymerase chain reaction.

RESULTS

One of the 33 children with autism spectrum disorder and intellectual disability - 3% of that group - had congenital CMV infection. The corresponding prevalence in newborn infants in Sweden is 0.2%. None of the 82 children without intellectual disability had congenital CMV.

CONCLUSION

The finding lends some further support for congenital CMV being one of the many aetiologies underlying autism spectrum disorder with intellectual disability. The rate of 3% of congenital CMV in children with autism spectrum disorder with intellectual disability has implications for the medical work-up. The finding of congenital CMV also indicates the need for repeated hearing assessments in the child. There is a need for similar studies with much larger samples.

摘要

目的

本研究旨在评估自闭症谱系障碍儿童代表性样本中先天性巨细胞病毒感染(CMV)的患病率。

方法

在115名患有自闭症谱系障碍的学龄前儿童代表性群体中,其中33名还患有智力障碍,使用TaqMan聚合酶链反应分析新生儿代谢筛查的干血斑中的CMV DNA。

结果

33名患有自闭症谱系障碍和智力障碍的儿童中有1名——该组的3%——患有先天性CMV感染。瑞典新生儿的相应患病率为0.2%。82名无智力障碍的儿童中无一例患有先天性CMV。

结论

这一发现进一步支持先天性CMV是导致伴有智力障碍的自闭症谱系障碍的众多病因之一。患有自闭症谱系障碍和智力障碍的儿童中先天性CMV的发生率为3%,这对医学检查有影响。先天性CMV的发现也表明需要对儿童进行反复听力评估。需要进行更大样本量的类似研究。

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