Evidence map›Paper›PMID 32523064›Full record

ArticleScientific reports2020

Placental Metabolomics for Assessment of Sex-specific Differences in Fetal Development During Normal Gestation.

Michelle Saoi, Katherine M Kennedy, Wajiha Gohir, Deborah M Sloboda, Philip Britz-McKibbin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
14.7field-weighted citation impact, top 1% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
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  5. Observational
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  16. Article
  17. The Placenta's Role in Sexually Dimorphic Fetal Growth Strategies.Reproductive sciences (Thousand Oaks, Calif.) · 2022
    Review
  18. Article
  19. Placental metabolite profiles in late gestation for healthy mice.Metabolomics : Official journal of the Metabolomic Society · 2022
    Article
  20. Review
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

5 authors at 2 institutions in 1 country.

Michelle SaoiDepartment of Chemistry and Chemical Biology, McMaster University, Hamilton, Canada.ORCID http://orcid.org/0000-0001-7678-6239
Katherine M KennedyDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.
Wajiha GohirDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.
Deborah M SlobodaDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.ORCID http://orcid.org/0000-0002-7410-4756
Philip Britz-McKibbinDepartment of Chemistry and Chemical Biology, McMaster University, Hamilton, Canada. britz@mcmaster.ca.
McMaster University · CAPopulation Health Research Institute · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The placenta is a metabolically active interfacial organ that plays crucial roles in fetal nutrient delivery, gas exchange and waste removal reflecting dynamic maternal and fetal interactions during gestation. There is growing evidence that the sex of the placenta influences fetal responses to external stimuli in utero, such as changes in maternal nutrition and exposure to environmental stressors. However, the exact biochemical mechanisms associated with sex-specific metabolic adaptations during pregnancy and its link to placental function and fetal development remain poorly understood. Herein, multisegment injection-capillary electrophoresis-mass spectrometry is used as a high throughput metabolomics platform to characterize lyophilized placental tissue (~2 mg dried weight) from C57BL/6J mice fed a standardized diet. Over 130 authentic metabolites were consistently measured from placental extracts when using a nontargeted metabolomics workflow with stringent quality control and robust batch correction. Our work revealed distinct metabolic phenotype differences that exist between male (n = 14) and female (n = 14) placentae collected at embryonic day E18.5. Intracellular metabolites associated with fatty acid oxidation and purine degradation were found to be elevated in females as compared to male placentae (p < 0.05, effect size >0.40), including uric acid, valerylcarnitine, hexanoylcarnitine, and 3-hydroxyhexanolycarnitine. This murine model sheds new insights into sex-specific differences in placental mitochondrial function and protective mechanisms against deleterious oxidative stress that may impact fetal growth and birth outcomes later in life.

Indexed as

AnimalsBody WeightFatty AcidsFemaleFetal DevelopmentFetusMaleMetabolomeMetabolomicsMiceMice, Inbred C57BLPlacentaPregnancyPurinesSex CharacteristicsFatty AcidspurinePurines

Identifiers

PMID32523064
PMCPMC7286906
OpenAlexW3034028120

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.