The contribution of paramagnetic rim and cortical lesions to physical and cognitive disability at multiple sclerosis clinical onset: evaluating the power of MRI and OCT biomarkers

被引:0
|
作者
Miscioscia, Alessandro [1 ,2 ,3 ]
Mainero, Caterina [1 ,4 ]
Treaba, Constantina A. [1 ,4 ]
Silvestri, Erica [5 ]
Scialpi, Graziana [3 ]
Berardi, Angela [3 ]
Causin, Francesco [6 ]
Anglani, Maria Giulia [6 ]
Rinaldi, Francesca [3 ]
Perini, Paola [3 ]
Puthenparampil, Marco [2 ,3 ]
Bertoldo, Alessandra [5 ]
Gallo, Paolo [2 ,3 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, A A Martinos Ctr Biomed Imaging, Dept Radiol, Bldg 149,13th St, Charlestown, MA 02129 USA
[2] Univ Padua, Dept Neurosci, Padua, Italy
[3] Padua Univ Hosp, Multiple Sclerosis Ctr Veneto Reg CeSMuV, Padua, Italy
[4] Harvard Med Sch, Boston, MA USA
[5] Univ Padua, Dept Informat Engn, Padua, Italy
[6] Padua Univ Hosp, Neuroradiol Unit, Padua, Italy
关键词
Paramagnetic rim lesion; Cortical lesion; Multiple sclerosis; Spinal cord; Optical coherence tomography; RELAPSING-REMITTING MS; WHITE-MATTER CHANGES; SPINAL-CORD; IMPAIRMENT; RECOMMENDATIONS; PATHOLOGY; RELEVANCE; ATROPHY;
D O I
10.1007/s00415-024-12622-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundIn multiple sclerosis (MS), imaging biomarkers play a crucial role in characterizing the disease at the time of diagnosis. MRI and optical coherence tomography (OCT) provide readily available biomarkers that may help to define the patient's clinical profile. However, the evaluation of cortical and paramagnetic rim lesions (CL, PRL), as well as retinal atrophy, is not routinely performed in clinic.ObjectiveTo identify the most significant MRI and OCT biomarkers associated with early clinical disability in MS.MethodsBrain, spinal cord (SC) MRI, and OCT scans were acquired from 45 patients at MS diagnosis to obtain: brain PRL and non-PRL, CL, SC lesion volumes and counts, brain volumetric metrics, SC C2-C3 cross-sectional area, and retinal layer thickness. Regression models assessed relationships with physical disability (Expanded Disability Status Scale [EDSS]) and cognitive performance (Brief International Cognitive Assessment for Multiple Sclerosis [BICAMS]).ResultsIn a stepwise regression (R2 = 0.526), PRL (beta = 0.001, p = 0.023) and SC lesion volumes (beta = 0.001, p = 0.017) were the most significant predictors of EDSS, while CL volume and age were strongly associated with BICAMS scores. Moreover, in a model where PRL and non-PRL were pooled, only the contribution of SC lesion volume was retained in EDSS prediction. OCT measures did not show associations with disability at the onset.ConclusionAt MS onset, PRL and SC lesions exhibit the strongest association with physical disability, while CL strongly contribute to cognitive performance. Incorporating the evaluation of PRL and CL into the initial MS patient assessment could help define their clinical profile, thus supporting the treatment choice.
引用
收藏
页码:6702 / 6714
页数:13
相关论文
共 50 条
  • [31] Rimnet: a deep 3D multimodal MRI architecture for paramagnetic rim lesions assessment in multiple sclerosis
    Barquero, G.
    La Rosa, F.
    Kebiri, H.
    Lu, P. -J.
    Rahmanzadeh, R.
    Weigel, M.
    Fartaria, M. J.
    Kober, T.
    Theaudin, M.
    Du Pasquier, R.
    Sati, P.
    Reich, D.
    Absinta, M.
    Granziera, C.
    Maggi, P.
    Cuadra, M. Bach
    MULTIPLE SCLEROSIS JOURNAL, 2020, 26 (3_SUPPL) : 36 - 36
  • [32] MRI-detectable cortical lesions in the cerebellum and their clinical relevance in multiple sclerosis
    Favaretto, Alice
    Lazzarotto, Andrea
    Poggiali, Davide
    Rolma, Giuseppe
    Causin, Francesco
    Rinaldi, Francesca
    Perini, Paola
    Gallo, Paolo
    MULTIPLE SCLEROSIS JOURNAL, 2016, 22 (04) : 494 - 501
  • [33] The clinical role of cortical lesions as a predicting factor for cognitive impairment in multiple sclerosis
    Curti, E.
    Graziuso, S.
    Tsantes, E.
    Crisi, G.
    Granella, F.
    MULTIPLE SCLEROSIS JOURNAL, 2016, 22 : 452 - 452
  • [34] Spatial distribution of cortical lesions in multiple sclerosis correlates to clinical and cognitive decline
    Bouman, P.
    Nguyen, N.
    Van Dam, M.
    Jonkman, L.
    Hulst, H.
    Geurts, J.
    Steenwijk, M.
    MULTIPLE SCLEROSIS JOURNAL, 2020, 26 (3_SUPPL) : 424 - 425
  • [35] The impact of paramagnetic rim lesions on cortical thickness and gray to white matter contrast in relapsing-remitting multiple sclerosis
    Xie, Yan
    Yao, Yihao
    Shen, Nanxi
    Li, Yuanhao
    Zhu, Hongquan
    Lu, Jun
    Liu, Dong
    Ding, Yujie
    Zhang, Yan
    Zhu, Wenzhen
    QUANTITATIVE IMAGING IN MEDICINE AND SURGERY, 2024, 14 (03)
  • [36] Evaluation of the Blood-Brain Barrier, Demyelination, and Neurodegeneration in Paramagnetic Rim Lesions in Multiple Sclerosis on 7 Tesla MRI
    Choi, Seongjin
    Lake, Sarah
    Harrison, Daniel M.
    JOURNAL OF MAGNETIC RESONANCE IMAGING, 2024, 59 (03) : 941 - 951
  • [37] Editorial for "Longitudinal Multi-Parametric Quantitative MRI Evaluation of Acute and Chronic Multiple Sclerosis Paramagnetic Rim Lesions"
    Zhang, Yue
    JOURNAL OF MAGNETIC RESONANCE IMAGING, 2025, 61 (04) : 1829 - 1830
  • [38] Editorial for "Evaluation of the Blood Brain Barrier, Demyelination, and Neurodegeneration of Paramagnetic Rim Lesions in Multiple Sclerosis on 7 Tesla MRI"
    Kauppinen, Risto A.
    JOURNAL OF MAGNETIC RESONANCE IMAGING, 2024, 59 (03) : 952 - 953
  • [39] Associations of MRI-lesions and clinical features with disability in Chinese patients with multiple sclerosis
    Cheng, Xiao-Juan
    Cheng, Qi
    Miao, Lin
    Guo, Zheng-Liang
    Guan, Yang-Tai
    Liu, Zhen-Guo
    Wang, Xin
    Sun, Xiao-Jiang
    Zhao, Zhong-Xin
    Song, Yong-Jian
    Ding, Xiao-Yi
    Chen, Sheng-Di
    Jiang, Guo-Xin
    Fredrikson, Sten
    NEUROLOGY ASIA, 2013, 18 (04) : 391 - 399
  • [40] Associations of MRI-lesions and clinical features with disability in Chinese patients with multiple sclerosis
    Cheng, X-J
    Cheng, Q.
    Miao, L.
    Guo, Z-L
    Guan, Y-T
    Liu, Z-G
    Wang, X.
    Sun, X-J
    Zhao, Z-X
    Song, Y-J
    Ding, X-Y
    Jiang, G-X
    Chen, S-D
    Fredrikson, S.
    EUROPEAN JOURNAL OF NEUROLOGY, 2010, 17 : 486 - 486