Leptomeningeal enhancement in multiple sclerosis: a focus on patients treated with hematopoietic stem cell transplantation

被引:2
作者
Marchi, Leonardo [1 ]
Mariottini, Alice [1 ,2 ,3 ]
Viti, Vittorio [1 ]
Bianchi, Andrea [4 ]
Nozzoli, Chiara [5 ]
Repice, Anna Maria [2 ,3 ]
Boncompagni, Riccardo [5 ]
Ginestroni, Andrea [4 ]
Damato, Valentina [1 ,2 ,3 ]
Barilaro, Alessandro [2 ,3 ]
Chiti, Stefano [6 ]
Saccardi, Riccardo [5 ]
Fainardi, Enrico [4 ,7 ]
Massacesi, Luca [1 ,2 ,3 ]
机构
[1] Univ Florence, Dept Neurosci Drug & Child Hlth, Florence, Italy
[2] Careggi Univ Hosp, Dept Neurol 2, Florence, Italy
[3] Careggi Univ Hosp, Tuscan Reg Multiple Sclerosis Referral Ctr, Florence, Italy
[4] Careggi Univ Hosp, Neuroradiol Unit, Florence, Italy
[5] Careggi Univ Hosp, Cell Therapy & Transfus Med Unit, Florence, Italy
[6] Careggi Univ Hosp, Hlth Phys Unit, Florence, Italy
[7] Univ Florence, Dept Expt Clin & Biomed Sci, Florence, Italy
关键词
multiple sclerosis; leptomeningeal enhancement; magnetic resonance imaging; autologous hematopoietic stem cell transplantation; transplant; chronic inflammation; biomarker; MENINGEAL INFLAMMATION; FOLLICLES;
D O I
10.3389/fneur.2024.1373385
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background 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.Methods 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.Results 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; p = 0.405). In the AHSCT group, LME number correlated with age at AHSCT (R = 0.50; p = 0.014), but not with age at post-treatment MRI. In the longitudinal pilot study (n = 8), one LME disappeared following AHSCT in 1/4 patients, whereas LME number was unchanged in the remaining four pwMS from the CTRL group.Discussion 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.
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