Relationship between sodium and diffusion MRI metrics in multiple sclerosis
Sodium MRI can measure <i>in vivo</i> sodium concentrations in people with multiple sclerosis, but the extent to which these alterations reflect metabolic dysfunction in the absence of tissue damage or neuroaxonal loss remains uncertain. Increases in total sodium concentration and extracellular sodium concentration are believed to be indicative of tissue disruption and extracellular space expansion. Conversely, increase in intracellular sodium concentration may represent early and transient responses to neuronal insult, preceding overt tissue damage. Here, we explored the relationship between total sodium concentration, intracellular sodium concentration and intracellular sodium volume fraction, which reflects extracellular sodium concentration, against histology-validated microstructural metrics obtained using diffusion MRI. Fifty-two individuals with multiple sclerosis and 26 healthy controls underwent <sup>1</sup>H/<sup>23</sup>Na MRI. Microstructural parameters were derived using Diffusion Basis Spectrum Imaging and Neurite Orientation Dispersion and Density-Imaging models. A progressive worsening in total sodium concentration and intracellular sodium volume fraction was observed from HCs white matter to normal-appearing white matter and further into T2-hyperintense and T1-hypointense lesions. Both total sodium concentration and intracellular sodium volume fraction, but not intracellular sodium concentration, correlated with Neurite Orientation Dispersion and Density Imaging and Diffusion Basis Spectrum Imaging metrics within multiple sclerosis lesions. Our findings confirm the utility of total sodium concentration and extracellular sodium concentration as indicators of extracellular expansion and axonal loss and underscore intracellular sodium concentration as a valuable biomarker for metabolic dysfunction in multiple sclerosis.
Authors
- Fernando E. Boada (ORCID: https://orcid.org/0000-0002-3289-9917)
- Fred Lublin (ORCID: https://orcid.org/0000-0001-5722-0475)
- Emilio Cipriano (ORCID: https://orcid.org/0000-0003-0304-0529)
- Sylvia Klineova (ORCID: https://orcid.org/0000-0002-0406-0460)
- Lazar Fleysher (ORCID: https://orcid.org/0000-0002-8727-2572)
- Maria Petracca (ORCID: https://orcid.org/0000-0001-9429-2769)
- Giacomo Boffa (ORCID: https://orcid.org/0000-0003-2220-9422)
- Nicole Graziano
- Matilde Inglese (ORCID: https://orcid.org/0000-0002-9610-0297)
- Simona Schiavi (ORCID: https://orcid.org/0000-0003-1641-186X)
- Gianluigi Mancardi (ORCID: https://orcid.org/0000-0001-8427-118X)
- Claire Wigley (ORCID: https://orcid.org/0009-0000-1825-8155)
Institutions
- Ospedale Policlinico San Martino (IT)
- University of Genoa (IT)
- Sapienza University of Rome (IT)
- Stanford University (US)
- Icahn School of Medicine at Mount Sinai (US)
Publication Details
- Journal
- Brain Communications
- Published
- 2024-12-24
- DOI
- https://doi.org/10.1093/braincomms/fcae446
- Citations
- 1
- Primary Topic
- Advanced Neuroimaging Techniques and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.40
Funders
- Ministero della Salute
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke