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dc.contributor.authorTanasescu, Radu
dc.contributor.authorConstantinescu, Cris S.
dc.date.accessioned2025-05-13T15:16:16Z
dc.date.available2025-05-13T15:16:16Z
dc.date.issued2023
dc.identifier.citationTanasescu, R., Mougin, O., Chou, I., Al-Radaideh, A., Jerca, O.P., Lim, S., Gowland, P. and Constantinescu, C.S. (2023) 'Natalizumab treatment for relapsing multiple sclerosis stabilises normal-appearing white matter microstructure: A one-year prospective ultra-high-field quantitative imaging study', Brain Sciences, 13(10), 1464. doi: 10.3390/brainsci13101464 https://doi.org/10.3390/brainsci13101464.en_US
dc.identifier.issn2076-3425
dc.identifier.issn2076-3425
dc.identifier.urihttp://hdl.handle.net/20.500.12904/19508
dc.description.abstract(1) Background: Natalizumab dramatically reduces relapses and MRI inflammatory activity (new lesions and enhancing lesions) in multiple sclerosis (MS). Chemical exchange saturation transfer (CEST) MRI can explore brain tissue in vivo with high resolution and sensitivity. We investigated if natalizumab can prevent microstructural tissue damage progression measured with MRI at ultra-high field (7 Tesla) over the first year of treatment. (2) Methods: In this one-year prospective longitudinal study, patients with active relapsing-remitting MS were assessed clinically and scanned at ultra-high-field MRI at the time of their first natalizumab infusion, at 6 and 12 months, with quantitative imaging aimed to detect microstructural changes in the normal-appearing white matter (NAWM), including sequences sensitive to magnetisation transfer (MT) effects from amide proton transfer (MTRAPT) and the nuclear Overhauser effect (MTRNOE). (3) Results: 12 patients were recruited, and 10 patients completed the study. The difference in the T1 relaxation times at month 6 and month 12 of natalizumab treatment was not significant, suggesting the lack of accumulation of tissue damage, while improvements were seen in MTR (MTRAPT and MTRNOE measures) at month 12, suggesting a tissue repair effect. This paralleled the expected lack of clinical and radiological worsening of conventional MRI measures of disease activity (new lesions or gadolinium-enhancing lesions). (4) Conclusion(s): Natalizumab prevents microstructural brain damage and has effects suggesting an improved white matter microstructure measured at ultra-high field during the first year of treatment.Copyright © 2023 by the authors.
dc.description.urihttps://doi.org/10.3390/brainsci13101464en_US
dc.language.isoenen_US
dc.subjectMagnetic resonance imagingen_US
dc.subjectMultiple sclerosisen_US
dc.subjectNatalizumaben_US
dc.titleNatalizumab treatment for relapsing multiple sclerosis stabilises normal-appearing white matter microstructure: A one-year prospective ultra-high-field quantitative imaging studyen_US
dc.typeArticleen_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.3390/brainsci13101464en_US
rioxxterms.typeJournal Article/Reviewen_US
refterms.dateFCD2025-05-13T15:16:17Z
refterms.versionFCDVoR
refterms.dateFOA2025-05-13T15:16:17Z
refterms.panelUnspecifieden_US
html.description.abstract(1) Background: Natalizumab dramatically reduces relapses and MRI inflammatory activity (new lesions and enhancing lesions) in multiple sclerosis (MS). Chemical exchange saturation transfer (CEST) MRI can explore brain tissue in vivo with high resolution and sensitivity. We investigated if natalizumab can prevent microstructural tissue damage progression measured with MRI at ultra-high field (7 Tesla) over the first year of treatment. (2) Methods: In this one-year prospective longitudinal study, patients with active relapsing-remitting MS were assessed clinically and scanned at ultra-high-field MRI at the time of their first natalizumab infusion, at 6 and 12 months, with quantitative imaging aimed to detect microstructural changes in the normal-appearing white matter (NAWM), including sequences sensitive to magnetisation transfer (MT) effects from amide proton transfer (MTRAPT) and the nuclear Overhauser effect (MTRNOE). (3) Results: 12 patients were recruited, and 10 patients completed the study. The difference in the T1 relaxation times at month 6 and month 12 of natalizumab treatment was not significant, suggesting the lack of accumulation of tissue damage, while improvements were seen in MTR (MTRAPT and MTRNOE measures) at month 12, suggesting a tissue repair effect. This paralleled the expected lack of clinical and radiological worsening of conventional MRI measures of disease activity (new lesions or gadolinium-enhancing lesions). (4) Conclusion(s): Natalizumab prevents microstructural brain damage and has effects suggesting an improved white matter microstructure measured at ultra-high field during the first year of treatment.Copyright © 2023 by the authors.en_US
rioxxterms.funder.project94a427429a5bcfef7dd04c33360d80cden_US


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