Evidence map›Paper›PMID 28879060›Full record

ArticlePeerJ2017

Onset of human preterm and term birth is related to unique inflammatory transcriptome profiles at the maternal fetal interface.

Radek Bukowski, Yoel Sadovsky, Hani Goodarzi, Heping Zhang, Joseph R Biggio, Michael Varner, Samuel Parry, Feifei Xiao, Sean M Esplin, William Andrews and 4 more

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 5 pooled it
6.9field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 5 syntheses or guidelines pooled it, 90 citations in OpenAlex.

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  11. Exosomal Delivery of Interleukin-10 Reduces Infection-Associated Inflammation in a 3D-Printed Model of a Humanized Feto-Maternal Interface.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  14. The landscape of decidual immune cells at the maternal-fetal interface in parturition and preterm birth.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 11 institutions in 1 country.

Radek BukowskiDell Medical School, Department of Women's Health, University of Texas at Austin, Austin, TX, United States of America.
Yoel SadovskyMagee-Womens Research Institute, University of Pittsburgh, Pittsburgh, PA, United States of America.
Hani GoodarziDepartment of Biophysics & Biochemistry, University of California, San Francisco, San Francisco, CA, United States of America.
Heping ZhangSchool of Public Health, Department of Biostatistics, Yale University, New Haven, CT, United States of America.
Joseph R BiggioSchool of Medicine, Department of Obstetrics and Gynecology, University of Alabama - Birmingham, Birmingham, AL, United States of America.
Michael VarnerSchool of Medicine, Intermountain Healthcare, Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, UT, United States of America.
Samuel ParrySchool of Medicine, Department of Obstetrics and Gynecology, University of Pennsylvania, Philadelphia, PA, United States of America.
Feifei XiaoArnold School of Public Health, Department of Epidemiology and Biostatistics, University of South Carolina, Columbia, SC, United States of America.
Sean M EsplinSchool of Medicine, Intermountain Healthcare, Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, UT, United States of America.
William AndrewsSchool of Medicine, Department of Obstetrics and Gynecology, University of Alabama - Birmingham, Birmingham, AL, United States of America.
George R SaadeDepartment of Obstetrics and Gynecology, University of Texas Medical Branch at Galveston, Galveston, TX, United States of America.
John V IlekisPregnancy and Perinatology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, United States of America.
Uma M ReddyPregnancy and Perinatology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, United States of America.
Donald A BaldwinSignal Biology Inc., Philadelphia, PA, United States of America.
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USIntermountain Healthcare · USUniversity of Alabama at Birmingham · USMagee-Womens Research Institute · USSignal Genetics (United States) · USThe University of Texas at Austin · USThe University of Texas Medical Branch at Galveston · USUniversity of California, San Francisco · USUniversity of Pennsylvania · USUniversity of South Carolina · USYale University · US

Funding

Data Management, Statistics, and informatics CoreU01HD050062 · NICHD · YALE UNIVERSITY · PI ZHANG, HEPING · 2005 to 2010
$5.1M
Network for Premature Birth Research Analytical CoreU01HD050088 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI PARRY, SAMUEL I. · 2006 to 2013
$4.1M
Genomic and Proteomic Network-Premature Birth ResearchU01HD050080 · NICHD · UNIVERSITY OF UTAH · PI VARNER, MICHAEL W. · 2006 to 2010
$2.3M
Genomic/Proteomic PTB Network: UAB Clinical Core CenterU01HD050094 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BIGGIO, JOSEPH RAMON · 2006 to 2010
$1.7M
Genomic/Proteomic Premature Birth Research Clinical CoreU01HD050078 · NICHD · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BUKOWSKI, RADEK K. · 2006 to 2010
$1.6M
NICHD NIH HHS U01 HD050062NICHD NIH HHS U01 HD050078NICHD NIH HHS U01 HD050080NICHD NIH HHS U01 HD050088NICHD NIH HHS U01 HD050094
6 · The paper itself

Abstract

backgroundPreterm birth is a main determinant of neonatal mortality and morbidity and a major contributor to the overall mortality and burden of disease. However, research of the preterm birth is hindered by the imprecise definition of the clinical phenotype and complexity of the molecular phenotype due to multiple pregnancy tissue types and molecular processes that may contribute to the preterm birth. Here we comprehensively evaluate the mRNA transcriptome that characterizes preterm and term labor in tissues comprising the pregnancy using precisely phenotyped samples. The four complementary phenotypes together provide comprehensive insight into preterm and term parturition.

methodsSamples of maternal blood, chorion, amnion, placenta, decidua, fetal blood, and myometrium from the uterine fundus and lower segment (

resultsThe largest differences in gene expression among the four groups occurred at maternal fetal interface in decidua, chorion and amnion. The gene expression profiles showed suppression of chemokines expression in TNL, withdrawal of this suppression in TL, activation of multiple pathways of inflammation in PL, and an immune rejection profile in PNL. The genes constituting expression signatures showed over-representation of three putative regulatory elements in their 5'and 3' UTR regions.

conclusionsThe results suggest that pregnancy is maintained by downregulation of chemokines at the maternal-fetal interface. Withdrawal of this downregulation results in the term birth and its overriding by the activation of multiple pathways of the immune system in the preterm birth. Complications of the pregnancy associated with impairment of placental function, which necessitated premature delivery of the fetus in the absence of labor, show gene expression patterns associated with immune rejection.

Indexed as

Gene expressionLaborPregnancyPretrem laborTranscriptomics

Identifiers

PMID28879060
PMCPMC5582610
OpenAlexW2752493287

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.