Quantitative MRI texture analysis in chronic active multiple sclerosis lesions

被引:9
作者
Weber, Claudia E. [1 ,2 ]
Wittayer, Matthias [1 ,2 ]
Kraemer, Matthias [3 ,4 ]
Dabringhaus, Andreas [4 ]
Platten, Michael [1 ,2 ]
Gass, Achim [1 ,2 ]
Eisele, Philipp [1 ,2 ]
机构
[1] Heidelberg Univ, Med Fac Mannheim, Dept Neurol, Theodor Kutzer Ufer 1-3, D-68167 Mannheim, Germany
[2] Heidelberg Univ, Mannheim Ctr Translat Neurosci MCTN, Theodor Kutzer Ufer 1-3, D-68167 Mannheim, Germany
[3] Hosp Zum Heiligen Geist, Dept Neurol & Neurol Early Rehabil, D-47906 Kempen, Germany
[4] Brainalyze GbR, Unterste Sauerwiese 9, D-51069 Cologne, Germany
关键词
multiple sclerosis; MRI; texture analysis; chronic active lesions; BRAIN; INSIGHTS; HETEROGENEITY; PERSISTENT; PATHOLOGY; IMAGES;
D O I
10.1016/j.mri.2021.03.016
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
Objective: Recently, there has been an increasing interest in "chronic enlarging" or "chronic active" multiple sclerosis (MS) lesions that are associated with clinical disability. However, investigation of dynamic lesion volume changes requires longitudinal MRI data from two or more time points. The aim of this study was to investigate the application of texture analysis (TA) on baseline T1-weighted 3D magnetization-prepared rapid acquisition gradient-echo (MPRAGE) images to differentiate chronic active from chronic stable MS lesions. Material and methods: To identify chronic active lesions as compared to non-enhancing stable lesions, two MPRAGE datasets acquired on a 3 T MRI at baseline and after 12 months follow-up were applied to the VoxelGuided Morphometry (VGM) algorithm. TA was performed on the baseline MPRAGE images, 36 texture features were extracted for each lesion. Results: Overall, 374 chronic MS lesions (155 chronic active and 219 chronic stable lesions) from 60 MS patients were included in the final analysis. Multiple texture features including "DISCRETIZED_HISTO_Energy", "GLCM_Energy", "GLCM_Contrast" and "GLCM_Dissimilarity" were significantly higher in chronic active as compared to chronic stable lesions. Partial least squares regression yielded an area under the curve of 0.7 to differentiate both lesion types. Conclusion: Our results suggest that multiple texture features extracted from MPRAGE images indicate higher intralesional heterogeneity, however they demonstrate only a fair accuracy to differentiate chronic active from chronic stable MS lesions.
引用
收藏
页码:97 / 102
页数:6
相关论文
共 39 条
[1]   Association of Chronic Active Multiple Sclerosis Lesions With Disability In Vivo [J].
Absinta, Martina ;
Sati, Pascal ;
Masuzzo, Federica ;
Nair, Govind ;
Sethi, Varun ;
Kolb, Hadar ;
Ohayon, Joan ;
Wu, Tianxia ;
Cortese, Irene C. M. ;
Reich, Daniel S. .
JAMA NEUROLOGY, 2019, 76 (12) :1474-1483
[2]   Persistent 7-tesla phase rim predicts poor outcome in new multiple sclerosis patient lesions [J].
Absinta, Martina ;
Sati, Pascal ;
Schindler, Matthew ;
Leibovitch, Emily C. ;
Ohayon, Joan ;
Wu, Tianxia ;
Meani, Alessandro ;
Filippi, Massimo ;
Jacobson, Steven ;
Cortese, Irene C. M. ;
Reich, Daniel S. .
JOURNAL OF CLINICAL INVESTIGATION, 2016, 126 (07) :2597-2609
[3]   Texture analysis in susceptibility-weighted imaging may be useful to differentiate acute from chronic multiple sclerosis lesions [J].
Caruana, Giovanni ;
Pessini, Lucas M. ;
Cannella, Roberto ;
Salvaggio, Giuseppe ;
de Barros, Andrea ;
Salerno, Annalaura ;
Auger, Cristina ;
Rovira, Alex .
EUROPEAN RADIOLOGY, 2020, 30 (11) :6348-6356
[4]   Multiple sclerosis [J].
Compston, A ;
Coles, A .
LANCET, 2002, 359 (9313) :1221-1231
[5]   Slow expansion of multiple sclerosis iron rim lesions: pathology and 7 T magnetic resonance imaging [J].
Dal-Bianco, Assunta ;
Grabner, Guenther ;
Kronnerwetter, Claudia ;
Weber, Michael ;
Hoeftberger, Romana ;
Berger, Thomas ;
Auff, Eduard ;
Leutmezer, Fritz ;
Trattnig, Siegfried ;
Lassmann, Hans ;
Bagnato, Francesca ;
Hametner, Simon .
ACTA NEUROPATHOLOGICA, 2017, 133 (01) :25-42
[6]   Atrophied Brain Lesion Volume: A New Imaging Biomarker in Multiple Sclerosis [J].
Dwyer, Michael G. ;
Bergsland, Niels ;
Ramasamy, Deepa P. ;
Jakimovski, Dejan ;
Weinstock-Guttman, Bianca ;
Zivadinov, Robert .
JOURNAL OF NEUROIMAGING, 2018, 28 (05) :490-495
[7]   Chronic white matter lesion activity predicts clinical progression in primary progressive multiple sclerosis [J].
Elliott, Colm ;
Belachew, Shibeshih ;
Wolinsky, Jerry S. ;
Hauser, Stephen L. ;
Kappos, Ludwig ;
Barkhof, Frederik ;
Bernasconi, Corrado ;
Fecker, Julian ;
Model, Fabian ;
Wei, Wei ;
Arnold, Douglas L. .
BRAIN, 2019, 142 :2787-2799
[8]   Slowly expanding/evolving lesions as a magnetic resonance imaging marker of chronic active multiple sclerosis lesions [J].
Elliott, Colm ;
Wolinsky, Jerry S. ;
Hauser, Stephen L. ;
Kappos, Ludwig ;
Barkhof, Frederik ;
Bernasconi, Corrado ;
Wei, Wei ;
Belachew, Shibeshih ;
Arnold, Douglas L. .
MULTIPLE SCLEROSIS JOURNAL, 2019, 25 (14) :1915-1925
[9]   MRI to monitor treatment efficacy in multiple sclerosis [J].
Fazekas, Franz ;
Soelberg-Sorensen, Per ;
Comi, Giancarlo ;
Filippi, Massimo .
JOURNAL OF NEUROIMAGING, 2007, 17 :50S-55S
[10]   Individual Assessment of Brain Tissue Changes in MS and the Effect of Focal Lesions on Short-Term Focal Atrophy Development in MS: A Voxel-Guided Morphometry Study [J].
Fox, Jan ;
Kraemer, Matthias ;
Schormann, Thorsten ;
Dabringhaus, Andreas ;
Hirsch, Jochen ;
Eisele, Philipp ;
Szabo, Kristina ;
Weiss, Christel ;
Amann, Michael ;
Weier, Katrin ;
Naegelin, Yvonne ;
Kappos, Ludwig ;
Gass, Achim .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (04) :1-15