Lesion phenotyping based on magnetic susceptibility in pediatric multiple sclerosis DOI
Vincenzo Daniele Boccia, Giacomo Boffa, Caterina Lapucci

et al.

Journal of Neuroimaging, Journal Year: 2024, Volume and Issue: 34(5), P. 567 - 571

Published: July 14, 2024

Abstract Background and purpose Pediatric multiple sclerosis (MS) displays different pathological features compared to adult MS, which can be studied in vivo by assessing tissue magnetic susceptibility with 3T‐MRI. We aimed assess white matter lesions (WMLs) phenotypes pediatric MS patients using quantitative mapping (QSM) weighted imaging (SMWI) over 12 months. Methods Eleven [female: 63.6%; mean ± standard deviation (SD) age disease duration: 16.3 2.2 2.4 1.5; median (range) Expanded Disability Status Scale (EDSS) 1 (0‐2)] underwent 3 Tesla‐MRI exams EDSS assessments at baseline after year. QSM SMWI were obtained 3‐dimensional (3D)‐segmented echo‐planar‐imaging submillimetric spatial resolution. WMLs classified according their appearance was used identify hyperintensities ascribable veins. Total brain volumes follow‐up computed high‐resolution 3D T1‐weighted images. Results Mean SD paramagnetic rim (PRLs) prevalence 7.0% 9.0. Fifty‐four percent (6/11) of exhibited least one PRL, patient exhibiting ≥ 4 PRLs. All showed QSM‐iso‐/hypo‐intense lesions, represented a 65.8% 22.7 total WMLs. QSM‐hyperintense positive correlation volume reduction ( r = 0.705; p .02). No lesion as between follow‐up. Conclusion Chronic compartmentalized inflammation seems occur early short duration. A high iso‐/hypo‐intense found, could account for the higher remyelination potential MS.

Language: Английский

Cognitive changes in patients with relapse-free MS treated with high efficacy therapies: the predictive value of paramagnetic rim lesions DOI
Vincenzo Daniele Boccia, Elisa Leveraro, Emilio Cipriano

et al.

Journal of Neurology Neurosurgery & Psychiatry, Journal Year: 2025, Volume and Issue: unknown, P. jnnp - 335144

Published: Jan. 31, 2025

Background High-efficacy disease-modifying therapies (HETs) have substantially improved multiple sclerosis (MS) management, yet ongoing cognitive decline remains a concern. This study aims to assess Symbol Digit Modalities Test (SDMT) changes in patients with stable relapsing-remitting MS (RRMS) treated HETs and evaluate the role of baseline MRI biomarkers as predictors SDMT changes. Methods Consecutive RRMS underwent clinical, assessment at clinical re-evaluation after 24 months. Patients presenting relapses or activity (new T2 and/or gadolinium-enhancing lesions) during follow-up were excluded. Cognitive defined using 90% CI regression-based reliable change index methodology accounting for sex, age, education score. Baseline examination included three-dimensional-sagittal Fluid Attenuated Inversion Recovery (FLAIR), T1-Magnetization Prepared - RApid Gradient Echo (T1-MPRAGE) quantitative susceptibility mapping (QSM) paramagnetic rim lesions (PRLs) QSM-isointense (ISO) assessment. Univariate multivariable regression analyses performed predict Results 90 (mean age: 40.3 years, median Expanded Disability Status Scale: 2.0) included. PRLs present 46 (51.1%) patients. After months, 13 (14.4%) showed 8 (8.9%) improvement. At analyses, associated higher risk (β: 2.70, p: 0.02, OR: 14.82) while ISO lesion volumes weakly improvement 0.07, 0.01, 1.07). Conclusions are detectable without over 2 years. seem MS, underscoring critical compartmentalised chronic inflammation disease progression.

Language: Английский

Citations

0

Biomarkers of Progression Independent of Relapse Activity—Can We Actually Measure It Yet? DOI Open Access
Gabriel Bsteh, Assunta Dal‐Bianco, Nik Krajnc

et al.

International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(10), P. 4704 - 4704

Published: May 14, 2025

Progression independent of relapse activity (PIRA) is increasingly recognized as a key driver disability in multiple sclerosis (MS). However, the concept PIRA remains elusive, with uncertainty surrounding its definition, underlying mechanisms, and methods quantification. This review examines current landscape biomarkers used to predict measure PIRA, focusing on clinical, imaging, body fluid biomarkers. Clinical scores such Expanded Disability Status Scale (EDSS) are widely used, but may lack sensitivity capturing subtle relapse-independent progression. Imaging biomarkers, including MRI-derived metrics (brain spinal cord volume loss, chronic active lesions) optical coherence tomography (OCT) parameters (retinal nerve fiber layer ganglion cell-inner plexiform thinning), offer valuable insights, often reflect both inflammatory neurodegenerative processes. Body neurofilament light chain (NfL) glial fibrillary acidic protein (GFAP), promising indicators axonal damage activation, their specificity for limited. emphasizes distinction between predicting PIRA—identifying individuals at risk future progression—and measuring ongoing PIRA-related real time. We highlight limitations differentiating from relapse-associated call clearer conceptual framework guide research. Advancing precision utility will require multimodal approaches, longitudinal studies, standardized protocols enable clinical integration improve personalized MS management.

Language: Английский

Citations

0

Lesion phenotyping based on magnetic susceptibility in pediatric multiple sclerosis DOI
Vincenzo Daniele Boccia, Giacomo Boffa, Caterina Lapucci

et al.

Journal of Neuroimaging, Journal Year: 2024, Volume and Issue: 34(5), P. 567 - 571

Published: July 14, 2024

Abstract Background and purpose Pediatric multiple sclerosis (MS) displays different pathological features compared to adult MS, which can be studied in vivo by assessing tissue magnetic susceptibility with 3T‐MRI. We aimed assess white matter lesions (WMLs) phenotypes pediatric MS patients using quantitative mapping (QSM) weighted imaging (SMWI) over 12 months. Methods Eleven [female: 63.6%; mean ± standard deviation (SD) age disease duration: 16.3 2.2 2.4 1.5; median (range) Expanded Disability Status Scale (EDSS) 1 (0‐2)] underwent 3 Tesla‐MRI exams EDSS assessments at baseline after year. QSM SMWI were obtained 3‐dimensional (3D)‐segmented echo‐planar‐imaging submillimetric spatial resolution. WMLs classified according their appearance was used identify hyperintensities ascribable veins. Total brain volumes follow‐up computed high‐resolution 3D T1‐weighted images. Results Mean SD paramagnetic rim (PRLs) prevalence 7.0% 9.0. Fifty‐four percent (6/11) of exhibited least one PRL, patient exhibiting ≥ 4 PRLs. All showed QSM‐iso‐/hypo‐intense lesions, represented a 65.8% 22.7 total WMLs. QSM‐hyperintense positive correlation volume reduction ( r = 0.705; p .02). No lesion as between follow‐up. Conclusion Chronic compartmentalized inflammation seems occur early short duration. A high iso‐/hypo‐intense found, could account for the higher remyelination potential MS.

Language: Английский

Citations

0