Quantitative susceptibility mapping of the normal-appearing white matter as a potential new marker of disability progression in multiple sclerosis

被引:6
作者
Pietroboni, Anna M. [1 ]
Colombi, Annalisa [1 ]
Contarino, Valeria E. [1 ]
Lo Russo, Francesco Maria [1 ]
Conte, Giorgio [1 ,2 ]
Morabito, Aurelia [3 ]
Siggillino, Silvia [1 ]
Carandini, Tiziana [1 ]
Fenoglio, Chiara [2 ]
Arighi, Andrea [1 ]
De Riz, Milena A. [1 ]
Arcaro, Marina [1 ]
Sacchi, Luca [2 ]
Fumagalli, Giorgio G. [1 ]
Bianchi, Anna Maria [4 ]
Triulzi, Fabio [1 ,2 ]
Scarpini, Elio [1 ]
Galimberti, Daniela [1 ,2 ]
机构
[1] Fdn IRCCS CaGranda Osped Maggiore Policlin, Via F Sforza 35, I-20122 Milan, Italy
[2] Univ Milan, Milan, Italy
[3] Ist Ric Farmacolog Mario Negri IRCCS, Milan, Italy
[4] Politecn Milan, Milan, Italy
关键词
Multiple sclerosis; Brain; White matter; Magnetic resonance imaging; Follow-up studies; HUMAN BRAIN; IRON; LESIONS; QSM;
D O I
10.1007/s00330-022-09338-6
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objectives To investigate the normal-appearing white matter (NAWM) susceptibility in a cohort of newly diagnosed multiple sclerosis (MS) patients and to evaluate possible correlations between NAWM susceptibility and disability progression.Methods Fifty-nine patients with a diagnosis of MS (n = 53) or clinically isolated syndrome (CIS) (n = 6) were recruited and followed up. All participants underwent neurological examination, blood sampling for serum neurofilament light chain (sNfL) level assessment, lumbar puncture for the quantification of cerebrospinal fluid (CSF) beta-amyloid1-42 (A beta) levels, and brain MRI. T2-weighted scans were used to quantify white matter (WM) lesion loads. For each scan, we derived the NAWM volume fraction and the WM lesion volume fraction. Quantitative susceptibility mapping (QSM) of the NAWM was calculated using the susceptibility tensor imaging (STI) suite. Susceptibility maps were computed with the STAR algorithm.Results Primary progressive patients (n = 9) showed a higher mean susceptibility value in the NAWM than relapsing-remitting (n = 44) and CIS (n = 6) (p = 0.01 and p = 0.02). Patients with a higher susceptibility in the NAWM showed increased sNfL concentration (rho = 0.38, p = 0.004) and lower CSF A beta levels (rho = -0.34, p = 0.009). Mean NAWM susceptibility turned out to be a predictor of the expanded disability status scale (EDSS) worsening at follow-up (beta = 0.41, t = 2.66, p = 0.01) and of the MS severity scale (MSSS) (0 = 0.38, t = 2.43, p = 0.019).Conclusions QSM in the NAWM seems to predict the EDSS increment over time. This finding might provide evidence on the role of QSM in identifying patients with an increased risk of early disability progression.
引用
收藏
页码:5368 / 5377
页数:10
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