Evidence map›Paper›PMID 37425859›Full record

ArticlebioRxiv : the preprint server for biology2023

Deep learning microstructure estimation of developing brains from diffusion MRI: a newborn and fetal study.

Hamza Kebiri, Ali Gholipour, Lana Vasung, Željka Krsnik, Davood Karimi, Meritxell Bach Cuadra

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Hamza KebiriCIBM Center for Biomedical Imaging, Switzerland.
Ali GholipourComputational Radiology Laboratory, Department of Radiology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Lana VasungDepartment of Pediatrics, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts, USA.
Željka KrsnikCroatian Institute for Brain Research, School of Medicine, University of Zagreb, Zagreb, Croatia.
Davood KarimiComputational Radiology Laboratory, Department of Radiology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Meritxell Bach CuadraCIBM Center for Biomedical Imaging, Switzerland.

Funding

Next-generation in-vivo fetal neuroimagingR01EB031849 · NIBIB · UNIVERSITY OF CALIFORNIA-IRVINE · PI GHOLIPOUR-BABOLI, ALI · 2021 to 2024
$2.2M
Imaging early development of human neural circuitsR01HD109395 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI ALI GHOLIPOUR-BABOLI · 2022 to 2026
$2.1M
Enhanced Imaging of the Fetal Brain MicrostructureR01EB032366 · NIBIB · UNIVERSITY OF CALIFORNIA-IRVINE · PI GHOLIPOUR-BABOLI, ALI · 2022 to 2025
$2.0M
Acquisition of a Siemens 3T MRI for Research ImagingS10OD025111 · OD · BOSTON CHILDREN'S HOSPITAL · PI WARFIELD, SIMON K · 2018 to 2018
$2.0M
Enabling the Assessment of Fetal Brain Development and Degeneration with Machine LearningR01NS128281 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Davood Karimi · 2023 to 2026
$1.8M
Advancing Microstructural and Vascular Neuroimaging in Perinatal StrokeR01NS106030 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI WARFIELD, SIMON K · 2019 to 2023
$1.7M
Accurate, reliable, and interpretable machine learning for assessment of neonatal and pediatric brain micro-structureR01HD110772 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Davood Karimi · 2023 to 2026
$1.5M
NIBIB NIH HHS R01 EB031849NIBIB NIH HHS R01 EB032366NICHD NIH HHS R01 HD109395NICHD NIH HHS R01 HD110772NIH HHS S10 OD025111NINDS NIH HHS R01 NS106030NINDS NIH HHS R01 NS128281
6 · The paper itself

Abstract

Diffusion-weighted magnetic resonance imaging (dMRI) is widely used to assess the brain white matter. Fiber orientation distribution functions (FODs) are a common way of representing the orientation and density of white matter fibers. However, with standard FOD computation methods, accurate estimation of FODs requires a large number of measurements that usually cannot be acquired for newborns and fetuses. We propose to overcome this limitation by using a deep learning method to map as few as six diffusion-weighted measurements to the target FOD. To train the model, we use the FODs computed using multi-shell high angular resolution measurements as target. Extensive quantitative evaluations show that the new deep learning method, using significantly fewer measurements, achieves comparable or superior results to standard methods such as Constrained Spherical Deconvolution. We demonstrate the generalizability of the new deep learning method across scanners, acquisition protocols, and anatomy on two clinical datasets of newborns and fetuses. Additionally, we compute agreement metrics within the HARDI newborn dataset, and validate fetal FODs with post-mortem histological data. The results of this study show the advantage of deep learning in inferring the microstructure of the developing brain from in-vivo dMRI measurements that are often very limited due to subject motion and limited acquisition times, but also highlight the intrinsic limitations of dMRI in the analysis of the developing brain microstructure. These findings, therefore, advocate for the need for improved methods that are tailored to studying the early development of human brain.

Identifiers

PMID37425859
PMCPMC10327173

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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.