Evidence map›Paper›PMID 25687564›Full record

Trial reportAmerican journal of obstetrics and gynecology2015

The phenotype of spontaneous preterm birth: application of a clinical phenotyping tool.

Tracy A Manuck, M Sean Esplin, Joseph Biggio, Radek Bukowski, Samuel Parry, Heping Zhang, Hao Huang, Michael W Varner, William Andrews, George Saade and 4 more

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in American journal of obstetrics and gynecology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

68 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Review
  8. Stress-induced developmental plasticity and spontaneous preterm birth: A justice-oriented eco-evo-devo review.European journal of obstetrics & gynecology and reproductive biology: X · 2025
    Review
  9. Article
  10. Review
  11. Maternal-fetal conflict and the timing of birth.Evolution, medicine, and public health · 2025
    Review
  12. Predictors of Inflammation-Mediated Preterm Birth.Physiology (Bethesda, Md.) · 2025
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Metabolomic profiling of preterm birth in pregnant women living with HIV.Metabolomics : Official journal of the Metabolomic Society · 2023
    Article

8 more citing papers are in PubMed but not listed here.

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.

Tracy A ManuckDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah School of Medicine, and Department of Maternal-Fetal Medicine, Intermountain Healthcare, Salt Lake City, UT. Electronic address: tmanuck@med.unc.edu.
M Sean EsplinDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah School of Medicine, and Department of Maternal-Fetal Medicine, Intermountain Healthcare, Salt Lake City, UT.
Joseph BiggioDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, and Center for Women's Reproductive Health, University of Alabama at Birmingham School of Medicine, Birmingham, AL.
Radek BukowskiDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, TX.
Samuel ParryDepartment of Obstetrics and Gynecology, University of Pennsylvania School of Medicine, Philadelphia, PA.
Heping ZhangCollaborative Center for Statistics in Science, Yale University School of Public Health, New Haven, CT.
Hao HuangCollaborative Center for Statistics in Science, Yale University School of Public Health, New Haven, CT.
Michael W VarnerDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah School of Medicine, and Department of Maternal-Fetal Medicine, Intermountain Healthcare, Salt Lake City, UT.
William AndrewsDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, and Center for Women's Reproductive Health, University of Alabama at Birmingham School of Medicine, Birmingham, AL.
George SaadeDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, TX.
Yoel SadovskyMagee-Womens Research Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Uma M ReddyPregnancy and Perinatology Branch, Center for Developmental Biology and Perinatal Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD.
John IlekisPregnancy and Perinatology Branch, Center for Developmental Biology and Perinatal Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD.
Eunice Kennedy Shriver National Institute of Child Health and Human Development Genomics and Proteomics Network for Preterm Birth Research

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
Pharmacogenomics of Preterm Birth Prevention and TreatmentK23HD067224 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MANUCK, TRACY A. · 2011 to 2015
$661k
NICHD NIH HHS 5K23HD067224NICHD NIH HHS K23 HD067224NICHD NIH HHS U01 HD050062NICHD NIH HHS U01-HD-050062NICHD NIH HHS U01 HD050078NICHD NIH HHS U01-HD-050078NICHD NIH HHS U01 HD050080NICHD NIH HHS U01-HD-050080NICHD NIH HHS U01 HD050088NICHD NIH HHS U01-HD-050088NICHD NIH HHS U01 HD050094NICHD NIH HHS U01-HD-050094
6 · The paper itself

Abstract

objectiveSpontaneous preterm birth (SPTB) is a complex condition that is likely a final common pathway with multiple possible causes. We hypothesized that a comprehensive classification system appropriately could group women with similar STPB causes and could provide an explanation, at least in part, for the disparities in SPTB that are associated with race and gestational age at delivery. STUDY

designThis was a planned analysis of a multicenter, prospective study of singleton SPTBs. Women with SPTB at <34 weeks' gestation were included. We defined 9 potential SPTB phenotypes based on clinical data: infection/inflammation, maternal stress, decidual hemorrhage, uterine distention, cervical insufficiency, placental dysfunction, premature rupture of the membranes, maternal comorbidities, and familial factors. Each woman's condition was evaluated for each phenotype. Delivery gestational age was compared between those with and without each phenotype. Phenotype profiles were also compared between women with very early (20.0-27.9 weeks' gestation) SPTB vs those with early SPTB (28.0-34.0 weeks' gestation) and between African American and white women. Statistical analysis was by t test and χ(2) test, as appropriate.

resultsThe phenotyping tool was applied to 1025 women with SPTBs who delivered at a mean 30.0 ± 3.2 (SD) weeks' gestation. Of these, 800 women (78%) had ≥2 phenotypes. Only 43 women (4.2%) had no phenotypes. The 281 women with early SPTBs were more likely to have infection/inflammation, decidual hemorrhage, and cervical insufficiency phenotypes (all P ≤ .001). African American women had more maternal stress and cervical insufficiency but less decidual hemorrhage and placental dysfunction compared with white women (all P < .05). Gestational age at delivery decreased as the number of phenotypes that were present increased.

conclusionPrecise SPTB phenotyping classifies women with SPTBs and identifies specific differences between very early and early SPTB and between African American and white women.

Indexed as

Gestational AgePhenotypeAdultCase-Control StudiesFemaleHumansPregnancyPremature BirthProspective StudiesRisk FactorsUnited Statesphenotypepretermracial disparityspontaneous preterm birth

Identifiers

PMID25687564
PMCPMC4456184

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Registered trials

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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.