Marchi Leonardo, Mariottini Alice, Viti Vittorio, Bianchi Andrea, Nozzoli Chiara, Repice Anna Maria, Boncompagni Riccardo, Ginestroni Andrea, Damato Valentina, Barilaro Alessandro, Chiti Stefano, Saccardi Riccardo, Fainardi Enrico, Massacesi Luca
Department of Neurosciences, Drug and Child Health, University of Florence, Florence, Italy.
Department of Neurology 2 and Tuscan Region Multiple Sclerosis Referral Center, Careggi University Hospital, Florence, Italy.
Front Neurol. 2024 Jun 5;15:1373385. doi: 10.3389/fneur.2024.1373385. eCollection 2024.
Leptomeningeal enhancement (LME) is considered an MRI marker of leptomeningeal inflammation in inflammatory neurological disorders, including multiple sclerosis (MS). To our knowledge, no disease-modifying therapies (DMTs) have been demonstrated to affect LME number or morphology so far.
Monocentric study investigating the frequency and number of LME in a cohort of people with (pw)MS who performed a 3 T brain MRI with a standardized protocol (including a post-contrast FLAIR sequence), and exploring the impact of autologous hematopoietic stem cell transplantation (AHSCT) on this marker. In a longitudinal pilot study, consecutive MRIs were also analyzed in a subgroup of pwMS, including patients evaluated both pre- and post-AHSCT.
Fifty-five pwMS were included: 24/55 (44%) had received AHSCT (AHSCT group) and 31 other treatments (CTRL group). At least one LME was identified in 19/55 (35%) cases (42 and 29% in the AHSCT and CTRL groups, respectively; = 0.405). In the AHSCT group, LME number correlated with age at AHSCT ( = 0.50; = 0.014), but not with age at post-treatment MRI. In the longitudinal pilot study ( = 8), one LME disappeared following AHSCT in 1/4 patients, whereas LME number was unchanged in the remaining four pwMS from the CTRL group.
These results suggest that AHSCT may affect development and persistence of LME, strengthening the indication for early use of effective therapies bioavailable within the central nervous system (CNS), and therefore potentially targeting compartmentalized inflammation.
软脑膜强化(LME)被认为是包括多发性硬化症(MS)在内的炎症性神经系统疾病中软脑膜炎症的MRI标志物。据我们所知,迄今为止,尚无疾病修饰疗法(DMTs)被证明会影响LME的数量或形态。
一项单中心研究,调查了一组采用标准化方案(包括对比后液体衰减反转恢复序列)进行3T脑部MRI检查的MS患者中LME的频率和数量,并探讨了自体造血干细胞移植(AHSCT)对该标志物的影响。在一项纵向试点研究中,还对一组MS患者的连续MRI进行了分析,包括在AHSCT前后均接受评估的患者。
纳入了55例MS患者:24/55(44%)接受了AHSCT(AHSCT组),另外31例接受了其他治疗(对照组)。19/55(35%)的病例中至少发现了一处LME(AHSCT组和对照组分别为42%和29%;P = 0.405)。在AHSCT组中,LME数量与AHSCT时的年龄相关(r = 0.50;P = 0.014),但与治疗后MRI时的年龄无关。在纵向试点研究(n = 8)中,1/4接受AHSCT的患者中有一处LME在AHSCT后消失,而对照组其余4例MS患者的LME数量未变。
这些结果表明,AHSCT可能会影响LME的发生和持续存在,强化了早期使用中枢神经系统(CNS)内可获得的有效疗法的指征,因此可能针对局限性炎症。