Natalizumab Treatment for Relapsing Multiple Sclerosis Stabilises Normal-Appearing White Matter Microstructure: A One-Year Prospective Ultra-High-Field Quantitative Imaging Study

Author:

Tanasescu Radu12ORCID,Mougin Olivier3ORCID,Chou I-Jun14,Al-Radaideh Ali356ORCID,Jerca Oltita P.17,Lim Su-Yin18,Gowland Penny3ORCID,Constantinescu Cris S.129ORCID

Affiliation:

1. Academic Unit of Mental Health and Clinical Neurosciences, Section of Clinical Neurology, University of Nottingham, Nottingham NG7 2UH, UK

2. Department of Neurology, Nottingham Centre for MS and Neuroinflammation, Nottingham University Hospitals NHS Trust, Nottingham NG5 1PB, UK

3. Sir Peter Mansfield Imaging Centre, School of Physics & Astronomy, University of Nottingham, Nottingham NG7 2QL, UK

4. Chang Gung Memorial Hospital, Linko Branch, Taoyuan 333, Taiwan

5. Department of Medical Imaging, Faculty of Applied Medical Sciences, The Hashemite University, Zarqa 13133, Jordan

6. Department of Medical Radiography, College of Health Sciences, University of Doha for Science and Technology, Doha 24449, Qatar

7. Medizinisches Zentrum Harz, 38820 Halberstadt, Germany

8. School of Medicine, Faculty of Health and Medical Sciences, Taylor’s University, Subang Jaya 47500, Malaysia

9. Cooper Neurological Institute, Cooper Medical School of Rowan University, Camden, NJ 08013, USA

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: 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.

Funder

an unrestricted research grant from Biogen-Idec UK

MRC

Publisher

MDPI AG

Subject

General Neuroscience

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