Selective inversion recovery quantitative magnetization transfer imaging: Toward a 3 T clinical application in multiple sclerosis

被引:18
作者
Bagnato, Francesca [1 ]
Franco, Giulia [1 ,2 ]
Ye, Fei [3 ]
Fan, Run [3 ]
Commiskey, Patricia [4 ]
Smith, Seth A. [5 ,6 ,7 ]
Xu, Junzhong [7 ,8 ]
Dortch, Richard [7 ,8 ]
机构
[1] VUMC, Dept Neurol, Div Neuroimmunol, Neuroimaging Unit, 2201 Childrens Way,Suite 1222, Nashville, TN 37212 USA
[2] Univ Milan, Dept Pathophysiol & Transplantat, Neurosci Sect, IRCCS Fdn Ca Granda Osped Maggiore Policlin,Dino, Milan, Italy
[3] VUMC, Dept Biostat, Nashville, TN 37212 USA
[4] VUMC, Dept Neurol, Stroke Div, Nashville, TN 37212 USA
[5] Vanderbilt Univ, Inst Imaging Sci, Dept Radiol & Radiol Sci, Nashville, TN USA
[6] Vanderbilt Univ, VUMC, Inst Imaging Sci, Dept Ophthalmol, Nashville, TN USA
[7] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37235 USA
[8] Vanderbilt Univ, Inst Imaging Sci, Dept Radiol & Radiol Sci, VLJMC, Nashville, TN USA
关键词
Biomarkers; demyelination; multiple sclerosis; outcome measurement; T2; lesions; APPEARING WHITE-MATTER; TRANSFER RATIO; HUMAN BRAIN; MRI; MODEL; DISABILITY; SEQUENCES; DIAGNOSIS; T-1;
D O I
10.1177/1352458519833018
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Assessing the degree of myelin injury in patients with multiple sclerosis (MS) is challenging due to the lack of magnetic resonance imaging (MRI) methods specific to myelin quantity. By measuring distinct tissue parameters from a two-pool model of the magnetization transfer (MT) effect, quantitative magnetization transfer (qMT) may yield these indices. However, due to long scan times, qMT has not been translated clinically. Objectives: We aim to assess the clinical feasibility of a recently optimized selective inversion recovery (SIR) qMT and to test the hypothesis that SIR-qMT-derived metrics are informative of radiological and clinical disease-related changes in MS. Methods: A total of 18 MS patients and 9 age- and sex-matched healthy controls (HCs) underwent a 3.0 Tesla (3 T) brain MRI, including clinical scans and an optimized SIR-qMT protocol. Four subjects were re-scanned at a 2-week interval to determine inter-scan variability. Results: SIR-qMT measures differed between lesional and non-lesional tissue (p < 0.0001) and between normal-appearing white matter (NAWM) of patients with more advanced disability and normal white matter (WM) of HCs (p < 0.05). SIR-qMT measures were associated with lesion volumes, disease duration, and disability scores (p <= 0.002). Conclusion: SIR-qMT at 3 T is clinically feasible and predicts both radiological and clinical disease severity in MS.
引用
收藏
页码:457 / 467
页数:11
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