Probabilistic mapping and automated segmentation of human brainstem white matter bundles

M Mark D. Olchanyi (Neuroscience Statistics Research Laboratory, Massachusetts Institute of Technology) D David R. Schreier (Neuroscience Statistics Research Laboratory, Massachusetts Institute of Technology) J Jian Li C Chiara Maffei (Center for Neurotechnology and Neurorecovery, Department of Neurology, Massachusetts General Hospital) A Annabel Sorby-Adams (Department of Neurology, Massachusetts General Hospital) H Hannah C. Kinney (Department of Pathology, Boston Children’s Hospital and Harvard Medical School) B Brian C. Healy (Department of Neurology, Massachusetts General Hospital) H Holly J. Freeman (Center for Neurotechnology and Neurorecovery, Department of Neurology, Massachusetts General Hospital) J Jared Shless (Neuroscience Statistics Research Laboratory, Massachusetts Institute of Technology) C Christophe Destrieux (Imaging Brain and Neuropsychiatry iBraiN U1253) H Henry Tregidgo (Hawkes Institute, University College London) J Juan Eugenio Iglesias E Emery N. Brown (Neuroscience Statistics Research Laboratory, Massachusetts Institute of Technology) B Brian L. Edlow

Abstract

Brainstem white matter (WM) bundles are essential conduits for neural signals that modulate homeostasis and consciousness. Their architecture forms the anatomic basis for brainstem connectomics, subcortical circuit models, and deep brain navigation tools. However, their small size and complex morphology, compared to cerebral WM, makes mapping and segmentation challenging in neuroimaging. As a result, fundamental questions about brainstem modulation of human homeostasis and consciousness remain unanswered. We leverage diffusion MRI tractography to create BrainStem Bundle Tool (BSBT), which automatically segments eight WM bundles in the rostral brainstem. BSBT performs segmentation on a custom probabilistic fiber map using a convolutional neural network architecture tailored to detect small anatomic structures. We demonstrate BSBT’s robustness across diffusion MRI acquisition protocols with in vivo scans of healthy subjects and ex vivo scans of human brain specimens with corresponding histology. BSBT also detected distinct brainstem bundle alterations in patients with Alzheimer’s disease, Parkinson’s disease, multiple sclerosis, and traumatic brain injury through tract-based analysis and classification tasks. Finally, we provide proof-of-principle evidence for the prognostic utility of BSBT in a longitudinal analysis of traumatic coma recovery. BSBT creates opportunities for scalable mapping of brainstem WM bundles and investigation of their role in a broad spectrum of neurological disorders.

Article Details

Volume / Issue Vol. 123, Issue 6
Published February 10, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (14)

M

Mark D. Olchanyi

Neuroscience Statistics Research Laboratory, Massachusetts Institute of Technology

D

David R. Schreier

Neuroscience Statistics Research Laboratory, Massachusetts Institute of Technology

J

Jian Li

C

Chiara Maffei

Center for Neurotechnology and Neurorecovery, Department of Neurology, Massachusetts General Hospital

A

Annabel Sorby-Adams

Department of Neurology, Massachusetts General Hospital

H

Hannah C. Kinney

Department of Pathology, Boston Children’s Hospital and Harvard Medical School

B

Brian C. Healy

Department of Neurology, Massachusetts General Hospital

H

Holly J. Freeman

Center for Neurotechnology and Neurorecovery, Department of Neurology, Massachusetts General Hospital

J

Jared Shless

Neuroscience Statistics Research Laboratory, Massachusetts Institute of Technology

C

Christophe Destrieux

Imaging Brain and Neuropsychiatry iBraiN U1253

H

Henry Tregidgo

Hawkes Institute, University College London

J

Juan Eugenio Iglesias

E

Emery N. Brown

Neuroscience Statistics Research Laboratory, Massachusetts Institute of Technology

B

Brian L. Edlow