Evidence map›Paper›PMID 42762266›Full record

ArticleBrain structure & function2026

Sex-related variability of white-matter tracts is robust to tractography methodology.

Matthew Amandola, Bastien Herlin, Michael E Kim, Simon Vandekar, Ivy Uszynski, Bennett Landman, Cyril Poupon, Kurt G Schilling

Abstract read
In one paragraph

Article in Brain structure & function, 2026. 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

8 authors.

Matthew AmandolaVanderbilt University Institute of Imaging Science, Nashville, TN, USA. matthew.amandola@vumc.org.
Bastien HerlinBAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA, Gif-Sur- Yvette, France.
Michael E KimDepartment of Computer Science, Vanderbilt University, Nashville, TN, USA.
Simon VandekarDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
Ivy UszynskiBAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA, Gif-Sur- Yvette, France.
Bennett LandmanVanderbilt University Institute of Imaging Science, Nashville, TN, USA.
Cyril PouponBAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA, Gif-Sur- Yvette, France.
Kurt G SchillingVanderbilt University Institute of Imaging Science, Nashville, TN, USA.

Funding

Postdoctoral Training in Biomedical MRI and MRST32EB001628 · NIBIB · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John C Gore · 2003 to 2026
$7.0M
Controlling Quality and Capturing Uncertainty in Advanced Diffusion Weighted MRIR01EB017230 · NIBIB · VANDERBILT UNIVERSITY · PI LANDMAN, BENNETT A. · 2015 to 2024
$5.1M
Semiparametric Inference for Psychiatric NeuroimagingR01MH123563 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI VANDEKAR, SIMON NEIL · 2020 to 2024
$2.1M
Microstructure and connectivity modeling from the cortex to the spinal cord in Multiple SclerosisK01EB032898 · NIBIB · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SCHILLING, KURT G · 2022 to 2025
$630k
European Union's Horizon 2020 Framework Program for Research and Innovation Grant No. 945539 (Human Brain Project SGA3)NIBIB NIH HHS K01 EB032898NIBIB NIH HHS R01 EB017230NIBIB NIH HHS T32 EB001628NIMH NIH HHS R01 MH123563
6 · The paper itself

Abstract

Diffusion tractography is the prominent in-vivo technique to study and investigate white-matter pathways in the human brain. While tractography is a powerful method, recent work suggests that different tractography methods can produce strikingly different representations of the same white-matter pathway. This multitude of differing options and diverging pipelines makes tractography related group-effects difficult to generalize, as it is currently unclear whether group-level inferences made using one tractography pipeline can be expected to hold when a different, equally defensible pipeline is applied to the same data. Here, we test the generalizability of sex-related changes on tractography-derived features by analyzing the exact same datasets with two equally reasonable pipelines which differ in model fitting, tractography reconstruction, and microstructure and volumetric analysis. We found that despite differences in analysis, the resulting patterns and biological interpretations of sex effects rarely disagreed across methods. Microstructural sex-related effects between methods were remarkably consistent between protocols, only displaying one statistically significant disagreement out of 343 comparisons (0.29%). However, discrepancies were more common among normalized pathway-volume effects, producing 8 out of the 9 total statistically significant disagreements between methods. Moreover, we found that the two tractography methods are differentially sensitive to tractography-derived features, as bundles derived from targeted tractography were much more sensitive to volumetric effects than tractogram-based tractography, potentially explaining the volumetric discrepancy between methods. This study indicates that reasonable methodological choices are unlikely to lead two investigators to fundamentally opposing conclusions about sex differences in white-matter, and that the robustness of tractography findings is similar to established fields of science. More broadly, this study presents an optimistic outlook on the future of tractography, and provides an initial empirical comparison of cross-pipeline robustness.

Indexed as

BrainDiffusion Tensor ImagingSex CharacteristicsWhite MatterAdultFemaleHumansImage Processing, Computer-AssistedMaleNeural PathwaysYoung AdultMicrostructureReproducibilitySex-effectsTractography

Identifiers

PMID42762266
PMCPMC13589754

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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.