Evidence map›Paper›PMID 38339954›Full record

ArticleHuman brain mapping2024

Estimating cortical thickness trajectories in children across different scanners using transfer learning from normative models.

C Gaiser, P Berthet, S M Kia, M A Frens, C F Beckmann, R L Muetzel, Andre F Marquand

Open access · goldAbstract read
In one paragraph

Article in Human brain mapping, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
20.0field-weighted citation impact, top 1% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

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  9. Lifespan Normative Modeling of Brain Microstructure.bioRxiv : the preprint server for biology · 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

7 authors at 4 institutions in 3 countries.

C GaiserDepartment of Neuroscience, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands.ORCID 0000-0003-3658-1946
P BerthetDepartment of Psychology, University of Oslo, Oslo, Norway.
S M KiaDonders Institute for Brain, Cognition, and Behavior, Radboud University, Nijmegen, The Netherlands.
M A FrensDepartment of Neuroscience, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands.
C F BeckmannDonders Institute for Brain, Cognition, and Behavior, Radboud University, Nijmegen, The Netherlands.
R L MuetzelDepartment of Child and Adolescent Psychiatry, Erasmus MC-Sophia Children's Hospital, University Medical Centre Rotterdam, Rotterdam, The Netherlands.
Andre F MarquandDonders Institute for Brain, Cognition, and Behavior, Radboud University, Nijmegen, The Netherlands.
Radboud University Nijmegen · NLErasmus MC · NLErasmus MC - Sophia Children’s Hospital · NLOslo University Hospital · NO

Funding

European Research Council 10100118Wellcome TrustWellcome Trust 215573/Z/19/ZWellcome Trust 215698/Z/19/ZZonMw
6 · The paper itself

Abstract

This work illustrates the use of normative models in a longitudinal neuroimaging study of children aged 6-17 years and demonstrates how such models can be used to make meaningful comparisons in longitudinal studies, even when individuals are scanned with different scanners across successive study waves. More specifically, we first estimated a large-scale reference normative model using Hierarchical Bayesian Regression from N = 42,993 individuals across the lifespan and from dozens of sites. We then transfer these models to a longitudinal developmental cohort (N = 6285) with three measurement waves acquired on two different scanners that were unseen during estimation of the reference models. We show that the use of normative models provides individual deviation scores that are independent of scanner effects and efficiently accommodate inter-site variations. Moreover, we provide empirical evidence to guide the optimization of sample size for the transfer of prior knowledge about the distribution of regional cortical thicknesses. We show that a transfer set containing as few as 25 samples per site can lead to good performance metrics on the test set. Finally, we demonstrate the clinical utility of this approach by showing that deviation scores obtained from the transferred normative models are able to detect and chart morphological heterogeneity in individuals born preterm.

Indexed as

Cerebral CortexMagnetic Resonance ImagingBayes TheoremBrainChildHumansInfant, NewbornMachine LearningNeuroimagingbrain agecortical thicknessMRIneurodevelopmentnormative modelling

Identifiers

PMID38339954
PMCPMC10839740
OpenAlexW4391613533

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.