Evidence map›Paper›PMID 28392167›Full record

ArticleDiabetes & metabolism2017

Associations between a fetal imprinted gene allele score and late pregnancy maternal glucose concentrations.

C J Petry, K Mooslehner, P Prentice, M G Hayes, M Nodzenski, D M Scholtens, I A Hughes, C L Acerini, K K Ong, W L Lowe and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetes & metabolism, 2017. 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
2.6field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Multigenerational diabetes mellitus.Frontiers in endocrinology · 2023
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Observational
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Ethnic Disparities in Gestational Diabetes.Current diabetes reports · 2018
    Review
  19. 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 4 institutions in 2 countries.

C J PetryDepartment of Paediatrics, Box 116, Addenbrooke's Hospital, University of Cambridge, Hills Road, CB2 0QQ Cambridge, UK. Electronic address: cjp1002@cam.ac.uk.
K MooslehnerDepartment of Paediatrics, Box 116, Addenbrooke's Hospital, University of Cambridge, Hills Road, CB2 0QQ Cambridge, UK.
P PrenticeDepartment of Paediatrics, Box 116, Addenbrooke's Hospital, University of Cambridge, Hills Road, CB2 0QQ Cambridge, UK.
M G HayesDivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
M NodzenskiDivision of Biostatistics, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
D M ScholtensDivision of Biostatistics, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
I A HughesDepartment of Paediatrics, Box 116, Addenbrooke's Hospital, University of Cambridge, Hills Road, CB2 0QQ Cambridge, UK.
C L AceriniDepartment of Paediatrics, Box 116, Addenbrooke's Hospital, University of Cambridge, Hills Road, CB2 0QQ Cambridge, UK.
K K OngDepartment of Paediatrics, Box 116, Addenbrooke's Hospital, University of Cambridge, Hills Road, CB2 0QQ Cambridge, UK; Medical Research Council Epidemiology Unit, University of Cambridge, Cambridge, UK.
W L LoweDivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
D B DungerDepartment of Paediatrics, Box 116, Addenbrooke's Hospital, University of Cambridge, Hills Road, CB2 0QQ Cambridge, UK; Medical Research Laboratories, The Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
University of Cambridge · GBNorthwestern University · USAddenbrooke's Hospital · GBMedical Research Council · GB

Funding

Hyperglycemia and Adverse Pregnancy Outcome (HAPO)R01HD034243 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI METZGER, BOYD E · 1999 to 2010
$16.2M
HAPO: DATA COORDINATING CENTERR01HD034242 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DYER, ALAN R · 1999 to 2007
$3.0M
GWA Mapping: Maternal Metabolism-Birth Weight InteractionsU01HG004415 · NHGRI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2007 to 2009
$1.1M
Replication of GWAS for Maternal Glycemia, Birthweight and their InteractionR01CA141688 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2009 to 2009
$399k
Biotechnology and Biological Sciences Research Council BB/F02293X/1Diabetes UK 11/0004241Medical Research Council G0500733Medical Research Council G0600717Medical Research Council G1001995Medical Research Council MC_UU_12015/2NCI NIH HHS R01 CA141688NHGRI NIH HHS U01 HG004415NICHD NIH HHS R01 HD034242NICHD NIH HHS R01 HD034243Wellcome Trust
6 · The paper itself

Abstract

aimWe hypothesised that some of the genetic risk for gestational diabetes (GDM) is due to the fetal genome affecting maternal glucose concentrations. Previously, we found associations between fetal IGF2 gene variants and maternal glucose concentrations in late pregnancy.

methodsIn the present study, we tested associations between SNP alleles from 15 fetal imprinted genes and maternal glucose concentrations in late pregnancy in the Cambridge Baby Growth and Wellbeing cohorts (1160 DNA trios).

resultsFour fetal SNP alleles with the strongest univariate associations: paternally-transmitted IGF2 rs10770125 (P-value=2×10

conclusionThis study suggests that polymorphic variation in fetal imprinted genes, particularly in the IGF2/INS region, contribute a small but significant part to the risk of raised late pregnancy maternal glucose concentrations.

Indexed as

AllelesGenomic ImprintingPolymorphism, Single NucleotideAdultBlood GlucoseDiabetes, GestationalFemaleHumansInsulinInsulin-Like Growth Factor IIKCNQ1 Potassium ChannelPregnancyPregnancy OutcomeBlood GlucoseIGF2 protein, humanInsulinInsulin-Like Growth Factor IIKCNQ1 Potassium ChannelGestational diabetesKCNQ1Meta-analysisPlacenta

Identifiers

PMID28392167
PMCPMC5507297
OpenAlexW2605367949

What OpenQuestion holds

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Registered trials

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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.