Evidence map›Paper›PMID 30157874›Full record

ArticleReproductive biology and endocrinology : RB&E2018

Associations between the maternal circulating lipid profile in pregnancy and fetal imprinted gene alleles: a cohort study.

Clive J Petry, Albert Koulman, Liangjian Lu, Benjamin Jenkins, Samuel Furse, Philippa Prentice, Lee Matthews, Ieuan A Hughes, Carlo L Acerini, Ken K Ong and 1 more

Open access · goldAbstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-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

8 citing papers in PubMed, 26 citations in OpenAlex.

  1. Hypoxia-Induced Suppression of FAM99A and FAM99B Contributes to the Development and Glucose Metabolic Reprogramming of Hepatocellular Carcinoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  7. Long non-coding RNA FAM99A modulated YAP1 to affect trophoblast cell behaviors in preeclampsia by sponging miR-134-5p.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  8. 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

11 authors at 2 institutions in 2 countries.

Clive J PetryDepartment of Paediatrics, University of Cambridge, Box 116, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0QQ, UK. cjp1002@cam.ac.uk.ORCID http://orcid.org/0000-0002-6642-9825
Albert KoulmanMedical Research Council Human Nutrition Research, Cambridge, UK.
Liangjian LuDepartment of Paediatrics, University of Cambridge, Box 116, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0QQ, UK.
Benjamin JenkinsMedical Research Council Human Nutrition Research, Cambridge, UK.
Samuel FurseThe Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
Philippa PrenticeDepartment of Paediatrics, University of Cambridge, Box 116, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0QQ, UK.
Lee MatthewsMedical Research Council Human Nutrition Research, Cambridge, UK.
Ieuan A HughesDepartment of Paediatrics, University of Cambridge, Box 116, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0QQ, UK.
Carlo L AceriniDepartment of Paediatrics, University of Cambridge, Box 116, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0QQ, UK.
Ken K OngDepartment of Paediatrics, University of Cambridge, Box 116, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0QQ, UK.
David B DungerDepartment of Paediatrics, University of Cambridge, Box 116, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0QQ, UK.
University of Cambridge · GBMRC Human Nutrition Research · GB

Funding

Diabetes UK 11/0004241Evelyn Trust EW9035322Fifth Framework Programme QLK4-1999-01422Medical Research Council G0800783Medical Research Council G1001995Medical Research Council MC_UU_12012/5Medical Research Council MC_UU_12015/Medical Research Council MC_UU_12015/2Medical Research Council MC_UU_12015/7Medical Research Council UD99999906Mothercare Charitable Foundation RG54608Newlife Foundation for Disabled Children 07/20Wellbeing of Women RG1644Wellcome TrustWorld Cancer Research Fund 2004/03
6 · The paper itself

Abstract

backgroundImprinted genes, which are expressed in a parent of origin-specific manner, are thought to mediate the genetic priorities of each parent in pregnancy. Recently we reported that some fetal imprinted gene variants are associated with maternal glucose concentrations and blood pressures in pregnancy. We suggest that the conflict between the effects of paternal and maternal transmitted genes starts at conception and may already be evident in measures of maternal metabolism in early pregnancy, before gestational diabetes is manifest.

methodsLipid fractions in maternal non-fasting serum collected around week 15 of pregnancy were profiled using direct infusion mass spectrometry in a subset Discovery Cohort (n = 200) of women from the Cambridge Baby Growth Study using direct infusion mass spectrometry. Associations between 151 haplotype-tag fetal polymorphisms in 16 imprinted genes and lipids were determined using partial least squares discriminant analysis. Variable importance in projection scores were used to identify those lipid species that contribute most to the underlying variation in the lipid profile and the concentrations of these species tested for associations with fetal imprinted gene alleles using linear regression. In an internal Validation Cohort (n = 567 women from the same cohort) the lipid fraction was profiled using liquid chromatography-mass spectrometry and tested for associations with the same fetal imprinted gene variants as above, followed by meta-analysis of associations from the Discovery and Validation Cohorts.

resultsThe most significant associations were between a monounsaturated triglyceride (44:1) and both paternally-transmitted fetal H19 rs7950932 (R = 0.14, p = 2.9 × 10

conclusionsFetal imprinted genes may influence maternal circulating clinically relevant triglyceride concentrations early in pregnancy.

Indexed as

Genomic ImprintingPolymorphism, Single NucleotideAdultAllelesCohort StudiesDiabetes, GestationalFemaleFetusGene FrequencyGenotypeHaplotypesHumansLipidsMass SpectrometryPregnancyLipidsDevelopmentGestational diabetesLipidomicsLipid profilingParent-of-originTriglycerides

Identifiers

PMID30157874
PMCPMC6116391
OpenAlexW2888858669

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.