Evidence map›Paper›PMID 24403553›Full record

ArticleThe Journal of infectious diseases2014

Intrauterine growth restriction caused by underlying congenital cytomegalovirus infection.

Lenore Pereira, Matthew Petitt, Alex Fong, Mitsuru Tsuge, Takako Tabata, June Fang-Hoover, Ekaterina Maidji, Martin Zydek, Yan Zhou, Naoki Inoue and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 2 pooled it
10.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 2 syntheses or guidelines pooled it, 119 citations in OpenAlex.

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  5. Joining the dots: maternal cytomegalovirus, HIV and the placenta.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 2 countries.

Lenore PereiraDepartment of Cell and Tissue Biology, School of Dentistry, University of California San Francisco, San Francisco, California.
Matthew Petitt
Alex Fong
Mitsuru Tsuge
Takako Tabata
June Fang-Hoover
Ekaterina Maidji
Martin Zydek
Yan Zhou
Naoki Inoue
Sanam Loghavi
Samuel Pepkowitz
Lawrence M Kauvar
Dotun Ogunyemi
University of California, San Francisco · USCedars-Sinai Medical Center · USNational Institute of Infectious Diseases · JPTrellis Bioscience (United States) · USUniversity of California, Irvine · USUniversity of California, Los Angeles · US

Funding

Fetal HCMV Infection: Role of the Human PlacentaR01AI046657 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PEREIRA, LENORE PALMA · 2000 to 2017
$5.9M
Therapeutic Antibodies for CMVR44AI102396 · NIAID · TRELLIS BIOSCIENCE, INC. · PI KAUVAR, LAWRENCE MICHAEL · 2012 to 2015
$3.3M
The role of CEACAM1 in CMV pathogenesis in the human placentaR21HD061890 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TABATA, TAKAKO · 2011 to 2012
$415k
Compensatory placental development after treatment for congenital CMV infectionR56AI073752 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PEREIRA, LENORE PALMA · 2008 to 2008
$386k
REGULATION OF TS CELL GROWTH AND DIFFERENTIATIONR01AI021420 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI RICH, SUSAN S · 1985 to 1991
–
NIAID NIH HHS R01 AI046657NIAID NIH HHS R01AI046657NIAID NIH HHS R01AI21420NIAID NIH HHS R44 AI102396NIAID NIH HHS R44AI102396NIAID NIH HHS R56 AI073752NIAID NIH HHS R56AI073752NIAID NIH HHS R56AI21739NICHD NIH HHS R21 HD061890NICHD NIH HHS R21HD061890
6 · The paper itself

Abstract

backgroundHuman cytomegalovirus (HCMV) is the major viral etiology of congenital infection and birth defects. Fetal transmission is high (30%-40%) in primary maternal infection, and symptomatic babies have permanent neurological, hearing, and vision defects. Recurrent infection is infrequently transmitted (2%) and largely asymptomatic. Congenital infection is also associated with intrauterine growth restriction (IUGR).

methodsTo investigate possible underlying HCMV infection in cases of idiopathic IUGR, we studied maternal and cord sera and placentas from 19 pregnancies. Anti-HCMV antibodies, hypoxia-related factors, and cmvIL-10 were measured in sera. Placental biopsy specimens were examined for viral DNA, expression of infected cell proteins, and pathology.

resultsAmong 7 IUGR cases, we identified 2 primary and 3 recurrent HCMV infections. Virus replicated in glandular epithelium and lymphatic endothelium in the decidua, cytotrophoblasts, and smooth muscle cells in blood vessels of floating villi and the chorion. Large fibrinoids with avascular villi, edema, and inflammation were significantly increased. Detection of viral proteins in the amniotic epithelium indicated transmission in 2 cases of IUGR with primary infection and 3 asymptomatic recurrent infections.

conclusionsCongenital HCMV infection impairs placental development and functions and should be considered as an underlying cause of IUGR, regardless of virus transmission to the fetus.

Indexed as

Antibodies, NeutralizingAntibodies, ViralCytomegalovirus InfectionsDNA, ViralFemaleFetal Growth RetardationHumansImmunoglobulin GInfant, NewbornInfectious Disease Transmission, VerticalPilot ProjectsPregnancyPregnancy Complications, InfectiousSerologic TestsAntibodies, NeutralizingAntibodies, ViralDNA, ViralImmunoglobulin Gamnionblood vesselschorioncongenitalfetusHCMVIUGRplacentapregnancyvilli

Identifiers

PMID24403553
PMCPMC3997585
OpenAlexW2159207059

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.