Evidence map›Paper›PMID 38130698›Full record

ArticleFrontiers in neuroscience2023

Characterization of dynamic patterns of human fetal to neonatal brain asymmetry with deformation-based morphometry.

Céline Steger, Charles Moatti, Kelly Payette, Alexandra De Silvestro, Thi Dao Nguyen, Seline Coraj, Ninib Yakoub, Giancarlo Natalucci, Raimund Kottke, Ruth Tuura and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Céline StegerCenter for MR Research, University Children's Hospital Zurich, University of Zurich, Zürich, Switzerland.
Charles MoattiCenter for MR Research, University Children's Hospital Zurich, University of Zurich, Zürich, Switzerland.
Kelly PayetteCenter for MR Research, University Children's Hospital Zurich, University of Zurich, Zürich, Switzerland.
Alexandra De SilvestroCenter for MR Research, University Children's Hospital Zurich, University of Zurich, Zürich, Switzerland.
Thi Dao NguyenNewborn Research, Department of Neonatology, University of Zurich and University Hospital Zurich, Zurich, Switzerland.
Seline CorajLarsson-Rosenquist Foundation Center for Neurodevelopment, Growth and Nutrition of the Newborn, Department of Neonatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Ninib YakoubLarsson-Rosenquist Foundation Center for Neurodevelopment, Growth and Nutrition of the Newborn, Department of Neonatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Giancarlo NatalucciNewborn Research, Department of Neonatology, University of Zurich and University Hospital Zurich, Zurich, Switzerland.
Raimund KottkeDepartment of Diagnostic Imaging, University Children's Hospital Zurich, University of Zurich, Zurich, Switzerland.
Ruth TuuraCenter for MR Research, University Children's Hospital Zurich, University of Zurich, Zürich, Switzerland.
Walter KnirschChildren's Research Center, University Children's Hospital Zurich, University of Zurich, Zurich, Switzerland.
Andras JakabCenter for MR Research, University Children's Hospital Zurich, University of Zurich, Zürich, Switzerland.
University of Zurich · CHUniversity Children's Hospital Zurich · CHUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Despite established knowledge on the morphological and functional asymmetries in the human brain, the understanding of how brain asymmetry patterns change during late fetal to neonatal life remains incomplete. The goal of this study was to characterize the dynamic patterns of inter-hemispheric brain asymmetry over this critically important developmental stage using longitudinally acquired MRI scans. Methods: Super-resolution reconstructed T2-weighted MRI of 20 neurotypically developing participants were used, and for each participant fetal and neonatal MRI was acquired. To quantify brain morphological changes, deformation-based morphometry (DBM) on the longitudinal MRI scans was utilized. Two registration frameworks were evaluated and used in our study: (A) fetal to neonatal image registration and (B) registration through a mid-time template. Developmental changes of cerebral asymmetry were characterized as (A) the inter-hemispheric differences of the Jacobian determinant (JD) of fetal to neonatal morphometry change and the (B) time-dependent change of the JD capturing left-right differences at fetal or neonatal time points. Left-right and fetal-neonatal differences were statistically tested using multivariate linear models, corrected for participants' age and sex and using threshold-free cluster enhancement. Results: Fetal to neonatal morphometry changes demonstrated asymmetry in the temporal pole, and left-right asymmetry differences between fetal and neonatal timepoints revealed temporal changes in the temporal pole, likely to go from right dominant in fetal to a bilateral morphology in neonatal timepoint. Furthermore, the analysis revealed right-dominant subcortical gray matter in neonates and three clusters of increased JD values in the left hemisphere from fetal to neonatal timepoints. Discussion: While these findings provide evidence that morphological asymmetry gradually emerges during development, discrepancies between registration frameworks require careful considerations when using DBM for longitudinal data of early brain development.

Indexed as

brain asymmetryDBM = deformation-based morphometryfetal brainlongitudinalmagnetic resonance imaging (MRI)neonatal brain

Identifiers

PMID38130698
PMCPMC10734644
OpenAlexW4389393103

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.