Tanasescu Radu, Mougin Olivier, Chou I-Jun, Al-Radaideh Ali, Jerca Oltita P, Lim Su-Yin, Gowland Penny, Constantinescu Cris S
Academic Unit of Mental Health and Clinical Neurosciences, Section of Clinical Neurology, University of Nottingham, Nottingham NG7 2UH, UK.
Department of Neurology, Nottingham Centre for MS and Neuroinflammation, Nottingham University Hospitals NHS Trust, Nottingham NG5 1PB, UK.
Brain Sci. 2023 Oct 17;13(10):1464. doi: 10.3390/brainsci13101464.
(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.
(1)背景:那他珠单抗可显著降低多发性硬化症(MS)的复发率以及磁共振成像(MRI)炎症活动(新病灶和强化病灶)。化学交换饱和转移(CEST)MRI能够以高分辨率和高灵敏度对脑组织进行活体检测。我们研究了那他珠单抗在治疗的第一年是否能预防通过超高场(7特斯拉)MRI检测到的脑组织微观结构损伤进展。(2)方法:在这项为期一年的前瞻性纵向研究中,对复发缓解型活动性MS患者在首次输注那他珠单抗时、6个月和12个月时进行临床评估,并采用超高场MRI扫描,通过定量成像检测正常白质(NAWM)中的微观结构变化,包括对酰胺质子转移(MTRAPT)和核Overhauser效应(MTRNOE)的磁化传递(MT)效应敏感的序列。(3)结果:招募了12名患者,10名患者完成了研究。那他珠单抗治疗6个月和12个月时T1弛豫时间的差异不显著,表明组织损伤没有累积,而在12个月时MTR(MTRAPT和MTRNOE测量值)有所改善,表明存在组织修复效应。这与疾病活动的传统MRI测量指标(新病灶或钆增强病灶)预期的临床和影像学无恶化情况相平行。(4)结论:那他珠单抗可预防脑微观结构损伤,并在治疗的第一年对超高场下测量的白质微观结构改善有作用。