TY - JOUR
T1 - Fully automated detection of paramagnetic rims in multiple sclerosis lesions on 3T susceptibility-based MR imaging
AU - Lou, Carolyn
AU - Sati, Pascal
AU - Absinta, Martina
AU - Clark, Kelly
AU - Dworkin, Jordan D.
AU - Valcarcel, Alessandra M.
AU - Schindler, Matthew K.
AU - Reich, Daniel S.
AU - Sweeney, Elizabeth M.
AU - Shinohara, Russell T.
N1 - Funding Information:
We thank the NINDS Neuroimmunology Clinic for recruiting and assessing the patients.
Funding Information:
Dr. Pascal Sati, Dr. Martina Absinta, and Dr. Daniel S. Reich are supported by the Intramural Research Program of the National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA. Dr. Martina Absinta is supported by the Conrad N. Hilton Foundation (grant#17313). Dr. Schindler is supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under award number KL2TR001879. Ms. Lou and Dr. Shinohara are supported by awards R01NS112274 and R01NS060910 from the National Institute of Neurological Disorders and Stroke, and R01MH112847 from the National Institute of Mental Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Funding Information:
A.M.V. is currently an employee of Genentech but did not receive funding or consulting fees as it pertains to this work. D.S.R. receives unrelated research funding from Vertex Pharmaceuticals. R.T.S. receives consulting fees from Octave Bioscience, and receives compensation for reviewing scientific articles from the American Medical Association and for reviewing grants for the Emerson Collective, National Institutes of Health, and the Department of Defense.
Publisher Copyright:
© 2021 The Authors
PY - 2021/1
Y1 - 2021/1
N2 - Background and Purpose: The presence of a paramagnetic rim around a white matter lesion has recently been shown to be a hallmark of a particular pathological type of multiple sclerosis lesion. Increased prevalence of these paramagnetic rim lesions is associated with a more severe disease course in MS, but manual identification is time-consuming. We present APRL, a method to automatically detect paramagnetic rim lesions on 3T T2*-phase images. Methods: T1-weighted, T2-FLAIR, and T2*-phase MRI of the brain were collected at 3T for 20 subjects with MS. The images were then processed with automated lesion segmentation, lesion center detection, lesion labelling, and lesion-level radiomic feature extraction. A total of 951 lesions were identified, 113 (12%) of which contained a paramagnetic rim. We divided our data into a training set (16 patients, 753 lesions) and a testing set (4 patients, 198 lesions), fit a random forest classification model on the training set, and assessed our ability to classify paramagnetic rim lesions on the test set. Results: The number of paramagnetic rim lesions per subject identified via our automated lesion labelling method was highly correlated with the gold standard count per subject, r = 0.86 (95% CI [0.68, 0.94]). The classification algorithm using radiomic features classified lesions with an area under the curve of 0.82 (95% CI [0.74, 0.92]). Conclusion: This study develops a fully automated technique, APRL, for the detection of paramagnetic rim lesions using standard T1 and FLAIR sequences and a T2*phase sequence obtained on 3T MR images.
AB - Background and Purpose: The presence of a paramagnetic rim around a white matter lesion has recently been shown to be a hallmark of a particular pathological type of multiple sclerosis lesion. Increased prevalence of these paramagnetic rim lesions is associated with a more severe disease course in MS, but manual identification is time-consuming. We present APRL, a method to automatically detect paramagnetic rim lesions on 3T T2*-phase images. Methods: T1-weighted, T2-FLAIR, and T2*-phase MRI of the brain were collected at 3T for 20 subjects with MS. The images were then processed with automated lesion segmentation, lesion center detection, lesion labelling, and lesion-level radiomic feature extraction. A total of 951 lesions were identified, 113 (12%) of which contained a paramagnetic rim. We divided our data into a training set (16 patients, 753 lesions) and a testing set (4 patients, 198 lesions), fit a random forest classification model on the training set, and assessed our ability to classify paramagnetic rim lesions on the test set. Results: The number of paramagnetic rim lesions per subject identified via our automated lesion labelling method was highly correlated with the gold standard count per subject, r = 0.86 (95% CI [0.68, 0.94]). The classification algorithm using radiomic features classified lesions with an area under the curve of 0.82 (95% CI [0.74, 0.92]). Conclusion: This study develops a fully automated technique, APRL, for the detection of paramagnetic rim lesions using standard T1 and FLAIR sequences and a T2*phase sequence obtained on 3T MR images.
KW - Multiple sclerosis
KW - Neuroimaging
KW - Paramagnetic rim lesions
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U2 - 10.1016/j.nicl.2021.102796
DO - 10.1016/j.nicl.2021.102796
M3 - Article
C2 - 34644666
AN - SCOPUS:85119587188
SN - 2213-1582
VL - 32
JO - NeuroImage: Clinical
JF - NeuroImage: Clinical
M1 - 102796
ER -