Evidence map›Paper›PMID 30391562›Full record

ArticleNeuroImage2019

A framework for multi-component analysis of diffusion MRI data over the neonatal period.

Maximilian Pietsch, Daan Christiaens, Jana Hutter, Lucilio Cordero-Grande, Anthony N Price, Emer Hughes, A David Edwards, Joseph V Hajnal, Serena J Counsell, J-Donald Tournier

Abstract read
In one paragraph

Article in NeuroImage, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–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

42 citing papers in PubMed.

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  6. Longitudinal trajectories of brain development from infancy to school age and their relationship with literacy development.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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.

Maximilian PietschCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK; Department of Biomedical Engineering, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK. Electronic address: maximilian.pietsch@kcl.ac.uk.
Daan ChristiaensCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK; Department of Biomedical Engineering, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.
Jana HutterCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK; Department of Biomedical Engineering, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.
Lucilio Cordero-GrandeCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK; Department of Biomedical Engineering, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.
Anthony N PriceCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK; Department of Biomedical Engineering, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.
Emer HughesCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.
A David EdwardsCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.
Joseph V HajnalCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK; Department of Biomedical Engineering, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.
Serena J CounsellCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.
J-Donald TournierCentre for the Developing Brain, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK; Department of Biomedical Engineering, School of Bioengineering and Imaging Sciences, Kings College London, Kings Health Partners, St. Thomas Hospital, London, SE1 7EH, UK.

Funding

Medical Research Council MR/K006355/1Medical Research Council MR/L011530/1Wellcome Trust 201374/Z/16/Z
6 · The paper itself

Abstract

We describe a framework for creating a time-resolved group average template of the developing brain using advanced multi-shell high angular resolution diffusion imaging data, for use in group voxel or fixel-wise analysis, atlas-building, and related applications. This relies on the recently proposed multi-shell multi-tissue constrained spherical deconvolution (MSMT-CSD) technique. We decompose the signal into one isotropic component and two anisotropic components, with response functions estimated from cerebrospinal fluid and white matter in the youngest and oldest participant groups, respectively. We build an orientationally-resolved template of those tissue components from data acquired from 113 babies between 33 and 44 weeks postmenstrual age, imaged as part of the Developing Human Connectome Project. These data were split into weekly groups, and registered to the corresponding group average templates using a previously-proposed non-linear diffeomorphic registration framework, designed to align orientation density functions (ODF). This framework was extended to allow the use of the multiple contrasts provided by the multi-tissue decomposition, and shown to provide superior alignment. Finally, the weekly templates were registered to the same common template to facilitate investigations into the evolution of the different components as a function of age. The resulting multi-tissue atlas provides insights into brain development and accompanying changes in microstructure, and forms the basis for future longitudinal investigations into healthy and pathological white matter maturation.

Indexed as

Diffusion Magnetic Resonance ImagingBrainConnectomeFemaleGestational AgeHumansImage Processing, Computer-AssistedInfant, NewbornInfant, PrematureMaleWhite MatterAtlasBrain developmentDiffusion MRIWhite matter

Identifiers

PMID30391562
PMCPMC6347572

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.