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Main Authors: Sandgaard, Anders Dyhr, Henriques, Rafael Neto, Shemesh, Noam, Jespersen, Sune Nørhøj
Format: Preprint
Published: 2025
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Online Access:https://arxiv.org/abs/2509.26267
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author Sandgaard, Anders Dyhr
Henriques, Rafael Neto
Shemesh, Noam
Jespersen, Sune Nørhøj
author_facet Sandgaard, Anders Dyhr
Henriques, Rafael Neto
Shemesh, Noam
Jespersen, Sune Nørhøj
contents In biological tissue, MR transverse relaxation stems from mechanisms spanning multiple scales, from molecular dipole-dipole interactions to mesoscopic field variations driven by tissue microstructure. While mesoscopic relaxation reflects cellular organization, its dynamics in white matter, specifically its dependence on axonal orientation and echo time, remain less investigated. This study employs theoretical frameworks and Monte-Carlo simulations using 3D EM-based white matter (WM) geometries to investigate how compartmentalization and realistic morphology drive these effects. Specifically, we simulate intra-axonal relaxation driven by magnetic fields induced by realistic axonal myelin sheaths and intra-axonal spheres as a model of iron-containing mitochondria. Our results confirm that orientation dependence of mesoscopic relaxation in WM is detectable and agrees with experimental observations. The time-dependence aligns with 1-dimensional short-range structural disorder, but at clinical echo times, this signature may be masked by dominant molecular relaxation. This work moves beyond idealized models to aid the development of more specific biophysical models of mesoscopic relaxation to achieve better biomarkers for neurodegenerative disease.
format Preprint
id arxiv_https___arxiv_org_abs_2509_26267
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Axonal microstructure and compartmentalization impact the orientation and time dependence of mesoscopic transverse relaxation
Sandgaard, Anders Dyhr
Henriques, Rafael Neto
Shemesh, Noam
Jespersen, Sune Nørhøj
Medical Physics
Biological Physics
In biological tissue, MR transverse relaxation stems from mechanisms spanning multiple scales, from molecular dipole-dipole interactions to mesoscopic field variations driven by tissue microstructure. While mesoscopic relaxation reflects cellular organization, its dynamics in white matter, specifically its dependence on axonal orientation and echo time, remain less investigated. This study employs theoretical frameworks and Monte-Carlo simulations using 3D EM-based white matter (WM) geometries to investigate how compartmentalization and realistic morphology drive these effects. Specifically, we simulate intra-axonal relaxation driven by magnetic fields induced by realistic axonal myelin sheaths and intra-axonal spheres as a model of iron-containing mitochondria. Our results confirm that orientation dependence of mesoscopic relaxation in WM is detectable and agrees with experimental observations. The time-dependence aligns with 1-dimensional short-range structural disorder, but at clinical echo times, this signature may be masked by dominant molecular relaxation. This work moves beyond idealized models to aid the development of more specific biophysical models of mesoscopic relaxation to achieve better biomarkers for neurodegenerative disease.
title Axonal microstructure and compartmentalization impact the orientation and time dependence of mesoscopic transverse relaxation
topic Medical Physics
Biological Physics
url https://arxiv.org/abs/2509.26267