Human gray matter microstructure mapped using neurite exchange imaging (NEXI) on a clinical scanner

Biophysical models of diffusion in gray matter (GM) can provide unique information about microstructure of the human brain, in health and disease. Therefore, their compatibility with clinical settings is key. Neurite Exchange Imaging (NEXI) is a two-compartment model of GM microstructure that accounts for inter-compartment exchange, whose parameter estimation requires multi-shell multi-diffusion time data. In this work, we report the first estimates of NEXI in human cortex obtained on a clinical MRI scanner. To do that, we establish an acquisition protocol and fitting routine compatible with clinical scanners. The model signal equation can be expressed either in the narrow-pulse approximation, NEXI, or accounting for the actual width of the diffusion gradient pulses, SMEX. While NEXI enables a faster analytical fit and is a valid approximation for data acquired on high-performance gradient systems (preclinical and Connectom scanners), on which NEXI was first implemented, SMEX has significant relevance for data acquired on clinical scanners with longer gradient pulses. We establish that, in the context of broad pulses, SMEX estimates were more comparable to previous literature values. Furthermore, we evaluate the repeatability of NEXI estimates in the human cortex on a clinical MRI scanner and show intra-subject variability to be lower than inter-subject variability, which is promising for characterizing healthy and patient cohorts. Finally, we analyze the relationship of NEXI parameters on the cortical surface to the Myelin Water Fraction (MWF), estimated using an established multicomponent T<sub>2</sub>relaxation technique. Indeed, although it is present in small quantities in the cortex, myelin can be expected to decrease permeability. We confirm a strong correlation between the exchange time (<i>t</i> <sub>ex</sub>) estimates and the MWF, although the spatial correspondence between the two is brain-region specific and other drivers of<i>t</i> <sub>ex</sub>than myelin density are likely at play.

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Publication Details

Journal
Imaging Neuroscience
Published
2025-01-01
DOI
https://doi.org/10.1162/imag.a.32
Citations
2
Primary Topic
Advanced Neuroimaging Techniques and Applications
Type
article
Field-Weighted Citation Impact
2.72

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article

Human gray matter microstructure mapped using neurite exchange imaging (NEXI) on a clinical scanner

Thorsten Feiweier, Gian Franco Piredda, Ileana Jelescu, Tommaso Pavan et al.
2 citations
Imaging Neuroscience
Advanced Neuroimaging Techniques and Applications
2.72
article

Human gray matter microstructure mapped using neurite exchange imaging (NEXI) on a clinical scanner

Thorsten Feiweier, Gian Franco Piredda, Ileana Jelescu, Tommaso Pavan, Quentin Uhl
article en
2 citations

Abstract

Biophysical models of diffusion in gray matter (GM) can provide unique information about microstructure of the human brain, in health and disease. Therefore, their compatibility with clinical settings is key. Neurite Exchange Imaging (NEXI) is a two-compartment model of GM microstructure that accounts for inter-compartment exchange, whose parameter estimation requires multi-shell multi-diffusion time data. In this work, we report the first estimates of NEXI in human cortex obtained on a clinical MRI scanner. To do that, we establish an acquisition protocol and fitting routine compatible with clinical scanners. The model signal equation can be expressed either in the narrow-pulse approximation, NEXI, or accounting for the actual width of the diffusion gradient pulses, SMEX. While NEXI enables a faster analytical fit and is a valid approximation for data acquired on high-performance gradient systems (preclinical and Connectom scanners), on which NEXI was first implemented, SMEX has significant relevance for data acquired on clinical scanners with longer gradient pulses. We establish that, in the context of broad pulses, SMEX estimates were more comparable to previous literature values. Furthermore, we evaluate the repeatability of NEXI estimates in the human cortex on a clinical MRI scanner and show intra-subject variability to be lower than inter-subject variability, which is promising for characterizing healthy and patient cohorts. Finally, we analyze the relationship of NEXI parameters on the cortical surface to the Myelin Water Fraction (MWF), estimated using an established multicomponent T<sub>2</sub>relaxation technique. Indeed, although it is present in small quantities in the cortex, myelin can be expected to decrease permeability. We confirm a strong correlation between the exchange time (<i>t</i> <sub>ex</sub>) estimates and the MWF, although the spatial correspondence between the two is brain-region specific and other drivers of<i>t</i> <sub>ex</sub>than myelin density are likely at play.

Imaging NeuroscienceVol. 3
Centre d'Imagerie BioMedicale (CH), Siemens Healthineers (Germany) (DE), Siemens (Switzerland) (CH), University of Lausanne (CH)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Centre d'Imagerie BioMédicale
Openalex Percentile: Top 11%
Advanced Neuroimaging Techniques and Applications
2.72
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