Cargando…

Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study

BACKGROUND: As congenital cytomegalovirus (CMV) infection causes significant clinical consequences not only at birth but also later as neurological sequelae, it is critical to establish a strategy for screening congenitally infected newborns. Previous studies have identified an insufficient sensitiv...

Descripción completa

Detalles Bibliográficos
Autores principales: Koyano, Shin, Inoue, Naoki, Oka, Akira, Moriuchi, Hiroyuki, Asano, Kimisato, Ito, Yushi, Yamada, Hideto, Yoshikawa, Tetsushi, Suzutani, Tatsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191411/
https://www.ncbi.nlm.nih.gov/pubmed/22021766
http://dx.doi.org/10.1136/bmjopen-2011-000118
_version_ 1782213651587923968
author Koyano, Shin
Inoue, Naoki
Oka, Akira
Moriuchi, Hiroyuki
Asano, Kimisato
Ito, Yushi
Yamada, Hideto
Yoshikawa, Tetsushi
Suzutani, Tatsuo
author_facet Koyano, Shin
Inoue, Naoki
Oka, Akira
Moriuchi, Hiroyuki
Asano, Kimisato
Ito, Yushi
Yamada, Hideto
Yoshikawa, Tetsushi
Suzutani, Tatsuo
author_sort Koyano, Shin
collection PubMed
description BACKGROUND: As congenital cytomegalovirus (CMV) infection causes significant clinical consequences not only at birth but also later as neurological sequelae, it is critical to establish a strategy for screening congenitally infected newborns. Previous studies have identified an insufficient sensitivity in screening methods based on the use of dried blood spots (DBSs). OBJECTIVES: To evaluate the feasibility of the authors' recently developed method for large-scale screening for congenital CMV infection and to identify risk factors for congenital infection. METHODS: More than 21 000 newborns were enrolled at 25 sites in six geographically separate areas of Japan. Urine was collected onto filter cards placed in the diapers, which were then analysed by quantitative PCR using the filter disc directly as a template. Clinical and physical findings of the newborns were extracted from their medical records. CMV strains from the cases and their siblings were genetically compared. Viral loads in DBSs obtained from some of the cases were compared with those in the urine filters. RESULTS: Congenital CMV infection was identified in 0.31% (95% CI 0.24% to 0.39%) of the newborns, and 30% of the cases (20/66) had typical clinical manifestations and/or showed abnormalities in brain images at birth. Although the positive predictive value of our screening was 94%, the lack of any comparison with a gold standard assay prevented calculation of the negative predictive value. Almost two-thirds of the cases had siblings, a significantly higher frequency than for uninfected newborns. Most of the cases (21/25) excreted CMV strains identical to those of their siblings. CMV DNA was undetectable in three out of 12 retrievable DBS specimens. CONCLUSIONS: Implementation of an effective large-scale screening programme for congenital CMV infection is feasible. Siblings are the major risk factor for congenital CMV infection, which emphasises the need for education of mothers-to-be as well as vaccine development.
format Online
Article
Text
id pubmed-3191411
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BMJ Group
record_format MEDLINE/PubMed
spelling pubmed-31914112011-10-13 Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study Koyano, Shin Inoue, Naoki Oka, Akira Moriuchi, Hiroyuki Asano, Kimisato Ito, Yushi Yamada, Hideto Yoshikawa, Tetsushi Suzutani, Tatsuo BMJ Open Infectious Diseases BACKGROUND: As congenital cytomegalovirus (CMV) infection causes significant clinical consequences not only at birth but also later as neurological sequelae, it is critical to establish a strategy for screening congenitally infected newborns. Previous studies have identified an insufficient sensitivity in screening methods based on the use of dried blood spots (DBSs). OBJECTIVES: To evaluate the feasibility of the authors' recently developed method for large-scale screening for congenital CMV infection and to identify risk factors for congenital infection. METHODS: More than 21 000 newborns were enrolled at 25 sites in six geographically separate areas of Japan. Urine was collected onto filter cards placed in the diapers, which were then analysed by quantitative PCR using the filter disc directly as a template. Clinical and physical findings of the newborns were extracted from their medical records. CMV strains from the cases and their siblings were genetically compared. Viral loads in DBSs obtained from some of the cases were compared with those in the urine filters. RESULTS: Congenital CMV infection was identified in 0.31% (95% CI 0.24% to 0.39%) of the newborns, and 30% of the cases (20/66) had typical clinical manifestations and/or showed abnormalities in brain images at birth. Although the positive predictive value of our screening was 94%, the lack of any comparison with a gold standard assay prevented calculation of the negative predictive value. Almost two-thirds of the cases had siblings, a significantly higher frequency than for uninfected newborns. Most of the cases (21/25) excreted CMV strains identical to those of their siblings. CMV DNA was undetectable in three out of 12 retrievable DBS specimens. CONCLUSIONS: Implementation of an effective large-scale screening programme for congenital CMV infection is feasible. Siblings are the major risk factor for congenital CMV infection, which emphasises the need for education of mothers-to-be as well as vaccine development. BMJ Group 2011-07-29 /pmc/articles/PMC3191411/ /pubmed/22021766 http://dx.doi.org/10.1136/bmjopen-2011-000118 Text en © 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Infectious Diseases
Koyano, Shin
Inoue, Naoki
Oka, Akira
Moriuchi, Hiroyuki
Asano, Kimisato
Ito, Yushi
Yamada, Hideto
Yoshikawa, Tetsushi
Suzutani, Tatsuo
Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study
title Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study
title_full Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study
title_fullStr Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study
title_full_unstemmed Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study
title_short Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study
title_sort screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study
topic Infectious Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191411/
https://www.ncbi.nlm.nih.gov/pubmed/22021766
http://dx.doi.org/10.1136/bmjopen-2011-000118
work_keys_str_mv AT koyanoshin screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT inouenaoki screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT okaakira screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT moriuchihiroyuki screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT asanokimisato screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT itoyushi screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT yamadahideto screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT yoshikawatetsushi screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT suzutanitatsuo screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy
AT screeningforcongenitalcytomegalovirusinfectionusingnewbornurinesamplescollectedonfilterpaperfeasibilityandoutcomesfromamulticentrestudy