Evidence map›Paper›PMID 28056489›Full record

ArticlePrenatal diagnosis2017

Use of high-frequency ultrasound to study the prenatal development of cranial neural tube defects and hydrocephalus in Gldc-deficient mice.

Maria C Autuori, Yun J Pai, Daniel J Stuckey, Dawn Savery, Anna M Marconi, Valentina Massa, Mark F Lythgoe, Andrew J Copp, Anna L David, Nicholas D E Greene

Open access · hybridAbstract read
In one paragraph

Article in Prenatal diagnosis, 2017. 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
0.9field-weighted citation impact, top 25% 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, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Study on the relationship between genetic polymorphism of reductive folic acid carrier and the risk of neural tube defects.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023
    Article
  4. Biomedicines · 2022
    Article
  5. Article
  6. Article
  7. 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

10 authors at 5 institutions in 3 countries.

Maria C AutuoriNewlife Birth Defects Research Centre and Developmental Biology and Cancer Programme, Great Ormond Street Institute of Child Health, University College London, London, UK.ORCID http://orcid.org/0000-0003-4107-325X
Yun J PaiNewlife Birth Defects Research Centre and Developmental Biology and Cancer Programme, Great Ormond Street Institute of Child Health, University College London, London, UK.ORCID http://orcid.org/0000-0001-7016-8667
Daniel J StuckeyCentre for Advanced Biomedical Imaging, University College London, London, UK.ORCID http://orcid.org/0000-0001-8888-627X
Dawn SaveryNewlife Birth Defects Research Centre and Developmental Biology and Cancer Programme, Great Ormond Street Institute of Child Health, University College London, London, UK.
Anna M MarconiDepartment of Obstetrics and Gynaecology, San Paolo Hospital, Milan, Italy.ORCID http://orcid.org/0000-0001-6295-1854
Valentina MassaDepartment of Health Science, San Paolo Hospital, Milan, Italy.
Mark F LythgoeCentre for Advanced Biomedical Imaging, University College London, London, UK.
Andrew J CoppNewlife Birth Defects Research Centre and Developmental Biology and Cancer Programme, Great Ormond Street Institute of Child Health, University College London, London, UK.ORCID http://orcid.org/0000-0002-2544-9117
Anna L DavidMaternal and Fetal Medicine, Institute for Women's Health, University College London, London, UK.ORCID http://orcid.org/0000-0002-0199-6140
Nicholas D E GreeneNewlife Birth Defects Research Centre and Developmental Biology and Cancer Programme, Great Ormond Street Institute of Child Health, University College London, London, UK.ORCID http://orcid.org/0000-0002-4170-5248
King's College London · GBAdvanced Imaging Research (United States) · USLondon Women's Clinic · GBOspedale San Paolo · ITOspedale San Paolo · IT

Funding

British Heart Foundation FS/15/33/31608Medical Research Council MR/J003794/1Medical Research Council MR/N003713/1Wellcome Trust 087525
6 · The paper itself

Abstract

objectiveWe used non-invasive high-frequency ultrasound (HFUS) imaging to investigate embryonic brain development in a mouse model for neural tube defects (NTDs) and non-ketotic hyperglycinemia (NKH).

methodUsing HFUS, we imaged embryos carrying loss of function alleles of Gldc encoding glycine decarboxylase, a component of the glycine cleavage system in mitochondrial folate metabolism, which is known to be associated with cranial NTDs and NKH in humans. We serially examined the same litter during the second half of embryonic development and quantified cerebral structures. Genotype was confirmed using PCR. Histology was used to confirm ultrasound findings.

resultsHigh-frequency ultrasound allowed in utero detection of two major brain abnormalities in Gldc-deficient mouse embryos, cranial NTDs (exencephaly) and ventriculomegaly (corresponding with the previous finding of post-natal hydrocephalus). Serial ultrasound allowed individual embryos to be analysed at successive gestational time points. From embryonic day 16.5 to 18.5, the lateral ventricle volume reduced in wild-type and heterozygous embryos but increased in homozygous Gldc-deficient embryos.

conclusionExencephaly and ventriculomegaly were detectable by HFUS in homozygous Gldc-deficient mouse embryos indicating this to be an effective tool to study CNS development. Longitudinal analysis of the same embryo allowed the prenatal onset and progression of ventricle enlargement in Gldc-deficient mice to be determined. © 2017 The Authors. Prenatal Diagnosis published by John Wiley & Sons, Ltd.

Indexed as

Ultrasonography, PrenatalAnimalsCentral Nervous SystemEmbryo, MammalianFemaleGlycine Dehydrogenase (Decarboxylating)HydrocephalusMiceMice, Inbred C57BLMice, KnockoutNeural Tube DefectsPregnancySkullGlycine Dehydrogenase (Decarboxylating)

Identifiers

PMID28056489
PMCPMC5347903
OpenAlexW2614102824

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.