Evidence map›Paper›PMID 26493725›Full record

ArticleBMC medical genomics2015

Systems biology evaluation of cell-free amniotic fluid transcriptome of term and preterm infants to detect fetal maturity.

Beena D Kamath-Rayne, Yina Du, Maria Hughes, Erin A Wagner, Louis J Muglia, Emily A DeFranco, Jeffrey A Whitsett, Nathan Salomonis, Yan Xu

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
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  18. Next-generation sequencing and prenatal 'omics: advanced diagnostics and new insights into human development.Genetics in medicine : official journal of the American College of Medical Genetics · 2018
    Review
  19. Extracellular RNA in aging.Wiley interdisciplinary reviews. RNA · 2017
    Review
  20. Article
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

9 authors at 1 institution in 1 country.

Beena D Kamath-RaynePerinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Beena.Kamath-Rayne@cchmc.org.
Yina DuPerinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Yina.Du@cchmc.org.
Maria HughesPerinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. marhughes2010@gmail.com.
Erin A WagnerPerinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Erin.Wagner@cchmc.org.
Louis J MugliaPerinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Louis.Muglia@cchmc.org.
Emily A DeFrancoPerinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Emily.DeFranco@ucmail.uc.edu.
Jeffrey A WhitsettPerinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Jeffrey.Whitsett@cchmc.org.
Nathan SalomonisBiomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Nathan.Salomonis@cchmc.org.
Yan XuPerinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Yan.Xu@cchmc.org.
Cincinnati Children's Hospital Medical Center · US

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., KISSELA, BRETT M · 2015 to 2024
$37.5M
Progenitor Cell Biology Consortium Administrative Coordinating CenterU01HL099997 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI TERRIN, MICHAEL L · 2009 to 2015
$29.9M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR026314 · NCRR · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2009 to 2011
$14.3M
Transcriptional Programming of Asthma Related Pathology in Respiratory EpitheliaR01HL095580 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI WHITSETT, JEFFREY A · 2009 to 2017
$4.7M
"Lung MAP" Atlas Research CenterU01HL122642 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI POTTER, S. STEVEN, WHITSETT, JEFFREY A · 2014 to 2018
$3.9M
Airway Progenitor Cell Profileration and Differentiation During Lung RepairU01HL110964 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI STREETER, PHILIP R, WHITSETT, JEFFREY A · 2012 to 2016
$3.3M
Role of SREBP Network in Surfactant Lipid Homeostasis and Lung MaturationR01HL105433 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI XU, YAN · 2011 to 2014
$1.8M
Omics of Lung DiseasesK12HL119986 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI WHITSETT, JEFFREY A · 2013 to 2017
$1.3M
NCATS NIH HHS UL1 TR001425NCRR NIH HHS UL1 RR026314NHLBI NIH HHS HL105433NHLBI NIH HHS HL110964NHLBI NIH HHS HL122642NHLBI NIH HHS K12 HL119986NHLBI NIH HHS R01 HL095580NHLBI NIH HHS R01 HL105433NHLBI NIH HHS U01 HL099997NHLBI NIH HHS U01HL099997NHLBI NIH HHS U01 HL110964NHLBI NIH HHS U01 HL122642
6 · The paper itself

Abstract

backgroundAmniotic fluid (AF) is a proximal fluid to the fetus containing higher amounts of cell-free fetal RNA/DNA than maternal serum, thereby making it a promising source for identifying novel biomarkers that predict fetal development and organ maturation. Our aim was to compare AF transcriptomic profiles at different time points in pregnancy to demonstrate unique genetic signatures that would serve as potential biomarkers indicative of fetal maturation.

methodsWe isolated AF RNA from 16 women at different time points in pregnancy: 4 from 18 to 24 weeks, 6 from 34 to 36 weeks, and 6 from 39 to 40 weeks. RNA-sequencing was performed on cell-free RNA. Gene expression and splicing analyses were performed in conjunction with cell-type and pathway predictions.

resultsSample-level analysis at different time points in pregnancy demonstrated a strong correlation with cell types found in the intrauterine environment and fetal respiratory, digestive and external barrier tissues of the fetus, using high-confidence cellular molecular markers. While some RNAs and splice variants were present throughout pregnancy, many transcripts were uniquely expressed at different time points in pregnancy and associated with distinct neonatal co-morbidities (respiratory distress and gavage feeding), indicating fetal immaturity.

conclusionThe AF transcriptome exhibits unique cell/organ-selective expression patterns at different time points in pregnancy that can potentially identify fetal organ maturity and predict neonatal morbidity. Developing novel biomarkers indicative of the maturation of multiple organ systems can improve upon our current methods of fetal maturity testing which focus solely on the lung, and will better inform obstetrical decisions regarding delivery timing.

Indexed as

Gene Expression ProfilingInfant, PrematureSystems BiologyAmniotic FluidComorbidityFemaleFetal Organ MaturityHumansMalePregnancySequence Analysis, RNATerm Birth

Identifiers

PMID26493725
PMCPMC4619218
OpenAlexW2176679849

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.