# Diffusion tractography outside the brain: the road less travelled

**Authors:** Kurt G. Schilling, Irvin Teh, Julien Cohen-Adad, Richard Dortch, Ibrahim Ibrahim, Nian Wang, Bruce Damon, Rory L. Cochran, Alexander Leemans

PMC · DOI: 10.1007/s00429-025-03062-9 · Brain Structure & Function · 2026-01-05

## TL;DR

This paper explores how diffusion tractography, a brain imaging technique, is being adapted to study other body tissues, offering new insights into their structure.

## Contribution

The paper surveys and details the methodological adaptations for applying tractography to anatomical structures outside the brain.

## Key findings

- Tractography has been successfully applied to the heart, spinal cord, and peripheral nerves.
- Adaptations are needed to address challenges like physiological motion and lower anisotropy in non-brain tissues.
- The technique provides non-invasive insights into tissue micro-organization for research and clinical use.

## Abstract

Diffusion tractography is a powerful MRI technique for mapping fibrous tissue architecture, traditionally applied to the white matter of the brain. This report surveys the growing application of tractography to anatomical structures outside the brain, a domain that presents both unique challenges and unique opportunities. We examine its use in the heart, spinal cord, peripheral nerves, brachial plexus, kidney, skeletal muscle, and prostate. For each region, we detail the necessary methodological adaptations for acquisition, modeling, and processing, and highlight the unique anatomical information that can be derived for research and clinical applications. While significant challenges remain - spanning technical hurdles like physiological motion and susceptibility artifacts, to biological complexities like lower anisotropy and the interpretation of streamline validity - tractography beyond the brain provides invaluable, non-invasive insights into tissue micro-organization, opening a new frontier for biomedical imaging.

## Full-text entities

- **Genes:** PDF (peptide deformylase, mitochondrial) [NCBI Gene 64146]
- **Diseases:** axonal loss (MESH:D012183), spinal muscular atrophy (MESH:D009134), chronic kidney disease (MESH:D051436), nerve damage (MESH:D000080902), arrhythmia (MESH:D001145), ischemic cardiomyopathy (MESH:D009202), inflammation (MESH:D007249), pelvic ring fractures (MESH:D012303), multifocal motor neuropathy (MESH:D000080364), Prostate cancer (MESH:D011471), MD (MESH:D008228), SCI (MESH:D013119), myocardial remodeling (MESH:D064752), crush injuries (MESH:D000071576), AD (MESH:C537791), pelvic fractures (MESH:D034161), injuries (MESH:D014947), edema (MESH:D004487), nerve sheath tumor (MESH:D018317), white-matter anomaly (MESH:D056784), spina bifida (MESH:D016135), neuropathies (MESH:D009422), cancer (MESH:D009369), fibrosis (MESH:D005355), FA (MESH:D054144), peripheral neuropathy (MESH:D010523), muscle damage (MESH:D009133), muscle disorders (MESH:D009135), C6 nerve root avulsion (MESH:D011843), pressure palsies (MESH:D010243), demyelination (MESH:D003711), infarct (MESH:D007238), atrophic forearm muscles (MESH:D005543), brachial plexopathy (MESH:D020516), hip dislocations (MESH:D006617), situs inversus totalis (MESH:D012857), neural tube defect (MESH:D009436), scarring (MESH:D002921), neurodegenerative diseases (MESH:D019636), intramedullary tumor (MESH:D013120)
- **Chemicals:** Water (MESH:D014867), FA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Bos taurus (bovine, species) [taxon 9913], Ovis aries (domestic sheep, species) [taxon 9940], Rattus norvegicus (brown rat, species) [taxon 10116], Sus scrofa (pig, species) [taxon 9823], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12769612/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12769612/full.md

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Source: https://tomesphere.com/paper/PMC12769612