Evidence map›Paper›PMID 33398476›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2021

Glycerophospholipid and detoxification pathways associated with small for gestation age pathophysiology: discovery metabolomics analysis in the SCOPE cohort.

Aude-Claire Morillon, Debora F B Leite, Shirish Yakkundi, Lee A Gethings, Gregoire Thomas, Philip N Baker, Louise C Kenny, Jane A English, Fergus P McCarthy

Open access · hybridAbstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Review
  7. 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 6 institutions in 4 countries.

Aude-Claire MorillonINFANT Research Centre, Cork University Hospital, Wilton, Cork, Ireland.ORCID http://orcid.org/0000-0002-9692-9396
Debora F B LeiteFederal University of Pernambuco, Pernambuco, Brazil.
Shirish YakkundiINFANT Research Centre, Cork University Hospital, Wilton, Cork, Ireland.
Lee A GethingsWaters Corporation, Wimslow, UK.
Gregoire ThomasSQU4RE, 8800, Roeselare, Belgium.
Philip N BakerCollege of Life Sciences, University of Leicester, Leicester, UK.
Louise C KennyDepartment of Women's and Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Jane A EnglishINFANT Research Centre, Cork University Hospital, Wilton, Cork, Ireland.
Fergus P McCarthyINFANT Research Centre, Cork University Hospital, Wilton, Cork, Ireland. Fergus.mccarthy@ucc.ie.
University College Cork · IEInagro (Belgium) · BEManchester Academic Health Science Centre · GBUniversidade Estadual de Campinas (UNICAMP) · BRUniversity of Leicester · GBUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSmall for gestational age (SGA) may be associated with neonatal morbidity and mortality. Our understanding of the molecular pathways implicated is poor.

objectivesOur aim was to determine the metabolic pathways involved in the pathophysiology of SGA and examine their variation between maternal biofluid samples.

methodsPlasma (Cork) and urine (Cork, Auckland) samples were collected at 20 weeks' gestation from nulliparous low-risk pregnant women participating in the SCOPE study. Women who delivered an SGA infant (birthweight < 10th percentile) were matched to controls (uncomplicated pregnancies). Metabolomics (urine) and lipidomics (plasma) analyses were performed using ultra performance liquid chromatography-mass spectrometry. Features were ranked based on FDR adjusted p-values from empirical Bayes analysis, and significant features putatively identified.

resultsLipidomics plasma analysis revealed that 22 out of the 33 significantly altered lipids annotated were glycerophospholipids; all were detected in higher levels in SGA. Metabolomic analysis identified reduced expression of metabolites associated with detoxification (D-Glucuronic acid, Estriol-16-glucuronide), nutrient absorption and transport (Sulfolithocholic acid) pathways.

conclusionsThis study suggests higher levels of glycerophospholipids, and lower levels of specific urine metabolites are implicated in the pathophysiology of SGA. Further research is needed to confirm these findings in independent samples.

Indexed as

Metabolic Detoxication, Phase IMetabolic Networks and PathwaysMetabolomeMetabolomicsChromatography, LiquidCohort StudiesGlycerophospholipidsHumansInfant, Small for Gestational AgeLipid MetabolismLipidomicsMass SpectrometryGlycerophospholipidsFetal growth restrictionLipidomicsMetabolomicsPlacental insufficiencyPregnancy complicationSmall for gestational age infant

Identifiers

PMID33398476
PMCPMC7782411
OpenAlexW3119912082

What OpenQuestion holds

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LicenceCC BY
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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.