Evidence map›Paper›PMID 29622558›Full record

Observational studyAJNR. American journal of neuroradiology2018

Characteristic MR Imaging Findings of the Neonatal Brain in RASopathies.

M N Cizmeci, M Lequin, K D Lichtenbelt, D Chitayat, P Kannu, A G James, F Groenendaal, E Chakkarapani, S Blaser, L S de Vries

Abstract readObservational Study
In one paragraph

Observational study in AJNR. American journal of neuroradiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
  4. Article
  5. Article
  6. Review
  7. Observational
  8. Article
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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.

M N CizmeciFrom the Departments of Neonatology (M.N.C., F.G., L.S.d.V.).ORCID 0000-0001-6807-4266
M LequinPediatric Radiology (M.L.), Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0001-7488-1734
K D LichtenbeltDepartment of Medical Genetics (K.D.L.), University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0002-6370-9207
D ChitayatDivisions of Clinical and Metabolic Genetics (D.C., P.K.).ORCID 0000-0003-1944-7294
P KannuDivisions of Clinical and Metabolic Genetics (D.C., P.K.).ORCID 0000-0001-5655-9805
A G JamesNeonatology (A.G.J.).ORCID 0000-0002-1732-1607
F GroenendaalFrom the Departments of Neonatology (M.N.C., F.G., L.S.d.V.).ORCID 0000-0002-9284-1637
E ChakkarapaniDivision of Neonatology (E.C.), School of Clinical Sciences, St Michael's Hospital, University of Bristol, Bristol, UK.ORCID 0000-0003-3380-047X
S BlaserNeuroradiology (S.B.), Department of Diagnostic Imaging, The Hospital for Sick Children and Department of Paediatrics, University of Toronto, Toronto, Canada.ORCID 0000-0001-8891-5106
L S de VriesFrom the Departments of Neonatology (M.N.C., F.G., L.S.d.V.) l.s.devries@umcutrecht.nl.ORCID 0000-0002-7282-8304

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeNeuroimaging features in neonates with RASopathies are rarely reported, and to date, there are no neuroimaging studies conducted in this population. Our aim was to investigate the occurrence of supratentorial and posterior fossa abnormalities on brain MRIs of neonates with a RASopathy. MATERIALS AND

methodsAn observational case-control study of neonates with a confirmed RASopathy was conducted. The presence of an intraventricular and/or parenchymal hemorrhage and punctate white matter lesions and assessments of the splenium of the corpus callosum, gyrification of the cortical gray matter, and enlargement of the extracerebral space were noted. The vermis height, transverse cerebellar diameter, cranial base angle, tentorial angle, and infratentorial angle were measured.

resultsWe reviewed 48 brain MR studies performed at 3 academic centers in 3 countries between 2009 and 2017. Sixteen of these infants had a genetically confirmed RASopathy (group 1), and 32 healthy infants were enrolled as the control group (group 2). An increased rate of white matter lesions, extracerebral space enlargement, simplification of the cortical gyrification, and white matter abnormalities were seen in group 1 (

conclusionsNeonates with a RASopathy had characteristic structural and acquired abnormalities in the cortical gray matter, white matter, corpus callosum, cerebellum, and posterior fossa. This study provides novel neuroimaging findings on supratentorial and posterior fossa abnormalities in neonates with a RASopathy.

Indexed as

BrainCase-Control StudiesFemaleGerm-Line MutationHumansInfantInfant, NewbornInfant, Newborn, DiseasesMagnetic Resonance ImagingMaleNeuroimagingras ProteinsWhite Matterras Proteins

Identifiers

PMID29622558
PMCPMC7410618

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.