Evidence map›Paper›PMID 41163627›Full record

ArticleHuman brain mapping2025

Choice of Processing Pipelines for T1-Weighted Brain MRI Impacts Association and Prediction Analyses.

Elise Delzant, Olivier Colliot, Baptiste Couvy-Duchesne

Abstract read
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

3 authors.

Elise DelzantSorbonne Université, Institut du Cerveau - Paris Brain Institute, CNRS, Inria, Inserm, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris, France.ORCID 0009-0001-8700-1684
Olivier ColliotSorbonne Université, Institut du Cerveau - Paris Brain Institute, CNRS, Inria, Inserm, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris, France.ORCID 0000-0002-9836-654X
Baptiste Couvy-DuchesneSorbonne Université, Institut du Cerveau - Paris Brain Institute, CNRS, Inria, Inserm, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris, France.

Funding

Agence Nationale de la Recherche 101136607Agence Nationale de la Recherche ANR-10-IAIHU-06Agence Nationale de la Recherche ANR-19-P3IA-0001NMHRC 1161356University of Queensland
6 · The paper itself

Abstract

The growing availability of large neuroimaging datasets, such as the UK Biobank, provides new opportunities to improve robustness and reproducibility in brain imaging research. However, little is known about the extent to which MRI processing pipelines influence results. Using 39,655 T1-weighted MRI scans from the UK Biobank, we systematically compared five widely used gray-matter representations derived from three major software packages: FSL (volume-based), CAT12/SPM (volume- and surface-based), and FreeSurfer (cortical and subcortical surface-based). We assessed their impact on morphometricity (trait variance explained by brain features), susceptibility to imaging confounders, false positives, association findings, and prediction accuracy across 29 diverse traits, including lifestyle, metabolic, and disease-related variables. We found that all pipelines were sensitive to imaging confounders such as head motion, brain position, and signal-to-noise ratio, and many produced non-normal voxel or vertex distributions. FSL and FreeSurfer generally yielded higher morphometricity estimates, but each captured partially unique signals, leading to inconsistencies in brain regions identified across methods. Volume-based approaches tended to outperform surface-based ones, detecting more significant clusters, achieving higher replication rates, and producing stronger predictive performance. Small clusters (single voxels or vertices) were less reliable, suggesting caution in their interpretation. Among all methods, FSLVBM emerged as the most consistent all-rounder, maximizing morphometricity, replicability, and predictive accuracy. Our results highlight the strengths and limitations of commonly used processing pipelines, offering benchmarks to guide researchers in method selection. They further suggest that combining multiple pipelines may improve brain-based prediction by leveraging unique, complementary signals, and that careful treatment of imaging confounders is essential for robust large-scale neuroimaging analyses.

Indexed as

BrainGray MatterImage Processing, Computer-AssistedMagnetic Resonance ImagingNeuroimagingAdultAgedFemaleHumansMaleMiddle AgedReproducibility of ResultsUnited Kingdom

Identifiers

PMID41163627
PMCPMC12572822

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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.