Evidence map›Paper›PMID 27660926›Full record

ArticleScientific reports2016

Altered Biomarkers in Trophoblast Cells Obtained Noninvasively Prior to Clinical Manifestation of Perinatal Disease.

Jay M Bolnick, Hamid-Reza Kohan-Ghadr, Rani Fritz, Alan D Bolnick, Brian A Kilburn, Michael P Diamond, D Randall Armant, Sascha Drewlo

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–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

19 citing papers in PubMed.

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  18. Anti-angiogenesis and Preeclampsia in 2016.Current hypertension reports · 2017
    Review
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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

8 authors.

Jay M BolnickDepartment of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
Hamid-Reza Kohan-GhadrDepartment of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
Rani FritzDepartment of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
Alan D BolnickDepartment of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
Brian A KilburnDepartment of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
Michael P DiamondDepartment of Obstetrics and Gynecology, Georgia Regents University, Augusta, GA, USA.
D Randall ArmantDepartment of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
Sascha DrewloDepartment of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.

Funding

The Role of PPARγ in Human Placental Development and PreeclampsiaR01HL128628 · NHLBI · WAYNE STATE UNIVERSITY · PI DREWLO, SASCHA · 2015 to 2019
$1.9M
Genetic Analysis of Human First Trimester Trophoblast in Ongoing PregnanciesR21HD071408 · NICHD · WAYNE STATE UNIVERSITY · PI ARMANT, DAVID RANDALL, DIAMOND, MICHAEL PETER · 2012 to 2013
$406k
NHLBI NIH HHS R01 HL128628NICHD NIH HHS R21 HD071408
6 · The paper itself

Abstract

A contributing factor to poor placental perfusion, leading to intrauterine growth restriction and preeclampsia, is the failure of invading extravillous trophoblast (EVT) cells to remodel the maternal uterine arteries during the first and second trimesters of pregnancy. Noninvasive assessment of EVT cells in ongoing pregnancies is possible beginning three weeks after conception, using trophoblast retrieval and isolation from the cervix (TRIC). Seven proteins were semi-quantified by immunofluorescence microscopy in EVT cells obtained between gestational weeks 6 and 20 from pregnancies with normal outcomes (N = 29) and those with intrauterine growth restriction or preeclampsia (N = 12). Significant differences were measured in expression of PAPPA, FLT1, ENG, AFP, PGF, and LGALS14, but not LGALS13 or the lineage marker KRT7. These findings provide for the first time direct evidence of pathology-associated protein dysregulation in EVT cells during early placentation. The TRIC platform provides a novel approach to acquire molecular signatures of EVT cells that can be correlated with pregnancy outcome.

Identifiers

PMID27660926
PMCPMC5034887

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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.