Evidence map›Paper›PMID 29997303›Full record

ArticleJCI insight2018

Placental polyamine metabolism differs by fetal sex, fetal growth restriction, and preeclampsia.

Sungsam Gong, Ulla Sovio, Irving Lmh Aye, Francesca Gaccioli, Justyna Dopierala, Michelle D Johnson, Angela M Wood, Emma Cook, Benjamin J Jenkins, Albert Koulman and 4 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 3 pooled it
3.0field-weighted citation impact, top 8% 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

52 citing papers in PubMed, 3 syntheses or guidelines pooled it, 81 citations in OpenAlex.

  1. Pooled it
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  4. Review
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  13. Article
  14. The central role of creatine and polyamines in fetal growth restriction.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  15. Article
  16. The role of polyamine metabolism in cellular function and physiology.American journal of physiology. Cell physiology · 2024
    Review
  17. Conserved and divergent features of trophoblast stem cells.Journal of molecular endocrinology · 2024
    Review
  18. Article
  19. 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

14 authors at 5 institutions in 3 countries.

Sungsam GongDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Ulla SovioDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Irving Lmh AyeDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Francesca GaccioliDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Justyna DopieralaDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Michelle D JohnsonDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Angela M WoodDepartment of Public Health and Primary Care.
Emma CookDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Benjamin J JenkinsNIHR BRC Core Metabolomics and Lipidomics Laboratory, University of Cambridge, Cambridge, United Kingdom.
Albert KoulmanNIHR BRC Core Metabolomics and Lipidomics Laboratory, University of Cambridge, Cambridge, United Kingdom.
Robert A CaseroThe Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Miguel ConstânciaDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
D Stephen Charnock-JonesDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Gordon Cs SmithDepartment of Obstetrics and Gynaecology, NIHR Cambridge Comprehensive Biomedical Research Centre.
Institut des Sciences Cognitives Marc Jeannerod · FRComprehensive Clinical Research · USUniversity of Cambridge · GBJohns Hopkins University · USWellcome/MRC Institute of Metabolic Science · GB

Funding

Identification of novel spermine oxidase (SMOX) inhibitors as probes for an emerging chemoprevention targetR01CA204345 · NCI · JOHNS HOPKINS UNIVERSITY · PI CASERO, ROBERT A., WOSTER, PATRICK M · 2016 to 2020
$3.4M
British Heart Foundation RG/13/13/30194Medical Research Council G1100221Medical Research Council MC_UU_00014/4Medical Research Council MC_UU_12012/4Medical Research Council MC_UU_12012/5Medical Research Council MRC_MC_UU_12012/4Medical Research Council MR/K021133/1Medical Research Council MR/L003120/1NCI NIH HHS R01 CA204345
6 · The paper itself

Abstract

Preeclampsia and fetal growth restriction (FGR) are major causes of the more than 5 million perinatal and infant deaths occurring globally each year, and both are associated with placental dysfunction. The risk of perinatal and infant death is greater in males, but the mechanisms are unclear. We studied data and biological samples from the Pregnancy Outcome Prediction (POP) study, a prospective cohort study that followed 4,212 women having first pregnancies from their dating ultrasound scan through delivery. We tested the hypothesis that fetal sex would be associated with altered placental function using multiomic and targeted analyses. We found that spermine synthase (SMS) escapes X-chromosome inactivation (XCI) in the placenta and is expressed at lower levels in male primary trophoblast cells, and male cells were more sensitive to polyamine depletion. The spermine metabolite N1,N12-diacetylspermine (DiAcSpm) was higher in the female placenta and in the serum of women pregnant with a female fetus. Higher maternal serum levels of DiAcSpm increased the risk of preeclampsia but decreased the risk of FGR. To our knowledge, DiAcSpm is the first maternal biomarker to demonstrate opposite associations with preeclampsia and FGR, and this is the first evidence to implicate polyamine metabolism in sex-related differences in placentally related complications of human pregnancy.

Indexed as

Cell SurvivalFemaleFetal DevelopmentFetal Growth RetardationGene Expression RegulationGenes, X-LinkedGestational AgeHumansMalePlacentaPolyaminesPre-EclampsiaPregnancyPregnancy ComplicationsProspective StudiesRisk AssessmentPolyaminesSpermineSpermine SynthaseExpression profilingObstetrics/gynecologyPolyaminesReproductive Biology

Identifiers

PMID29997303
PMCPMC6124516
OpenAlexW2877486660

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.