Clinical feasibility of brain quantitative susceptibility mapping.

TitleClinical feasibility of brain quantitative susceptibility mapping.
Publication TypeJournal Article
Year of Publication2019
AuthorsZhang S, Liu Z, Nguyen TD, Yao Y, Gillen KM, Spincemaille P, Kovanlikaya I, Gupta A, Wang Y
JournalMagn Reson Imaging
Volume60
Pagination44-51
Date Published2019 07
ISSN1873-5894
KeywordsAdolescent, Adult, Aged, Aged, 80 and over, Algorithms, Brain, Brain Ischemia, Brain Mapping, Child, Child, Preschool, Feasibility Studies, Female, Glioma, Humans, Image Processing, Computer-Assisted, Imaging, Three-Dimensional, Infant, Infant, Newborn, Magnetic Resonance Imaging, Male, Middle Aged, Multiple Sclerosis, Nervous System Diseases, Pattern Recognition, Automated, Retrospective Studies, Stroke, Young Adult
Abstract

PURPOSE: To evaluate the quality of brain quantitative susceptibility mapping (QSM) that is fully automatically reconstructed in clinical MRI of various neurological diseases.

METHODS: 393 consecutive patients in one month were recruited for this evaluation study. QSM was reconstructed using Morphology Enabled Dipole Inversion without zero reference regularization (MEDI) and using MEDI with cerebrospinal fluid automatic zero-reference regularization to generate susceptibility values (MEDI+0). Two neuroradiologists independently assessed the image quality of MEDI+0 and MEDI and image concordance between them. Lesion susceptibility values were measured in 20 cases of glioma, 21 cases of ischemic stroke and 43 multiple sclerosis (MS) cases on both MEDI+0 and MEDI images.

RESULTS: The two neuroradiologists rated the MEDI+0 image qualities of the 393 cases as 351 (89.3%) and 362 (92.1%) excellent, 29 (7.4%) and 24 (6.1%) diagnostic, and 13 (3.3%) and 7 (1.8%) poor, and scored the concordances between MEDI+0 and MEDI as 364 (92.6%) and 351 (89.3%) excellent, 13 (3.3%) and 31 (7.9%) good, 14 (3.6%) and 9 (2.3%) intermediate, 2 (0.5%) and 2 (0.5%) poor, and 0 (0%) and 0 (0%) none. There was good correlation between MEDI+0 and MEDI in lesion susceptibility contrast of glioma, ischemic stroke, and MS cases (all p < 0.05). The MS lesion susceptibility time course from this patient cohort was found to be similar to the reported pattern: isointense initially for acute enhancing lesions, and hyperintense over the following years for active chronic lesions.

CONCLUSION: Brain QSM images of various neurological diseases have reliable diagnostic quality in clinical MRI, with MEDI+0 providing susceptibility values automatically referenced to CSF in longitudinal and cross-center studies.

DOI10.1016/j.mri.2019.04.003
Alternate JournalMagn Reson Imaging
PubMed ID30954651
PubMed Central IDPMC6535129
Grant ListR21 EB024366 / EB / NIBIB NIH HHS / United States
R01 NS090464 / NS / NINDS NIH HHS / United States
R01 NS095562 / NS / NINDS NIH HHS / United States
S10 OD021782 / OD / NIH HHS / United States
R01 CA181566 / CA / NCI NIH HHS / United States
Related Institute: 
MRI Research Institute (MRIRI)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065