Evidence map›Paper›PMID 41054966›Full record

ArticleHuman brain mapping2025

Deep Learning for fODF Estimation in Infant Brains: Model Comparison, Ground-Truth Impact, and Domain Shift Mitigation.

Rizhong Lin, Hamza Kebiri, Ali Gholipour, Yufei Chen, Jean-Philippe Thiran, Davood Karimi, Meritxell Bach Cuadra

Abstract readComparative Study
In one paragraph

Article in Human brain mapping, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Rizhong LinSignal Processing Laboratory (LTS5), École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.ORCID 0009-0000-1468-6734
Hamza KebiriDepartment of Diagnostic and Interventional Radiology, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.ORCID 0000-0001-7592-3166
Ali GholipourComputational Radiology Laboratory, Department of Radiology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0001-7699-4564
Yufei ChenSchool of Computer Science and Technology, Tongji University, Shanghai, China.ORCID 0000-0002-3645-9046
Jean-Philippe ThiranSignal Processing Laboratory (LTS5), École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.ORCID 0000-0003-2938-9657
Davood KarimiComputational Radiology Laboratory, Department of Radiology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0001-7277-9736
Meritxell Bach CuadraDepartment of Diagnostic and Interventional Radiology, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.ORCID 0000-0003-2730-4285

Funding

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
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
Eunice Kennedy Shriver National Institute of Child Health and Human Development R01HD110772National Natural Science Foundation of China 62472315NICHD NIH HHS R01 HD110772NINDS NIH HHS R01 NS128281NINDS NIH HHS R01NS128281Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 182602Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 215641US National Institutes of Health
6 · The paper itself

Abstract

The accurate estimation of fiber orientation distribution functions (fODFs) in diffusion magnetic resonance imaging (MRI) is crucial for understanding early brain development and its potential disruptions. Although supervised deep learning (DL) models have shown promise in fODF estimation from neonatal diffusion MRI (dMRI) data, the out-of-domain (OOD) performance of these models remains largely unexplored, especially under diverse domain shift scenarios. This study evaluated the robustness of three state-of-the-art DL architectures: multilayer perceptron (MLP), transformer, and U-Net/convolutional neural network (CNN) on fODF predictions derived from dMRI data. Using 488 subjects from the developing Human Connectome Project (dHCP) and the Baby Connectome Project (BCP) datasets, we reconstructed reference fODFs from the full dMRI series using single-shell three-tissue constrained spherical deconvolution (SS3T-CSD) and multi-shell multi-tissue CSD (MSMT-CSD) to generate reference fODF reconstructions for model training, and systematically assessed the impact of age, scanner/protocol differences, and input dimensionality on model performance. Our findings reveal that U-Net consistently outperformed other models when fewer diffusion gradient directions were used, particularly with the SS3T-CSD-derived ground truth, which showed superior performance in capturing crossing fibers. However, as the number of input diffusion gradient directions increased, MLP and the transformer-based model exhibited steady gains in accuracy. Nevertheless, performance nearly plateaued from 28 to 45 input directions in all models. Age-related domain shifts showed asymmetric patterns, being less pronounced in late developmental stages (late neonates, and babies), with SS3T-CSD demonstrating greater robustness to variability compared to MSMT-CSD. To address inter-site domain shifts, we implemented two adaptation strategies: the Method of Moments (MoM) and fine-tuning. Both strategies achieved significant improvements (

Indexed as

BrainConnectomeDeep LearningDiffusion Magnetic Resonance ImagingDiffusion Tensor ImagingImage Processing, Computer-AssistedWhite MatterFemaleHumansInfantInfant, NewbornMaleNeural Networks, Computerconstrained spherical deconvolution (CSD)deep learningdiffusion MRIdomain adaptationdomain shiftfiber orientation distribution function (fODF)infantneonate

Identifiers

PMID41054966
PMCPMC12501774

What OpenQuestion holds

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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.