Literature DB >> 30286313

Diffusion tensor imaging and quantitative susceptibility mapping as diagnostic tools for motor neuron disorders.

Elizabeth K Weidman1, Andrew D Schweitzer1, Sumit N Niogi1, Emily J Brady1, Anna Starikov1, Gulce Askin2, Mona Shahbazi3, Yi Wang1, Dale Lange3, Apostolos John Tsiouris4.   

Abstract

PURPOSE: Diffusion tensor imaging (DTI) and quantitative susceptibility mapping (QSM) have been proposed as methods to aid in the diagnosis of amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS), both diseases affecting upper motor neurons. We test the performance of DTI and QSM alone and in combination to distinguish patients with diseases affecting upper motor neurons (ALS/PLS) from patients with other motor symptom-predominant neurologic disorders.
METHODS: 3.0 Tesla MRI with DTI and QSM in patients referred to a subspecialty neurology clinic for evaluation of motor symptom-predominant neurologic disorders were retrospectively reviewed. Corticospinal tract fractional anisotropy and maximum motor cortex susceptibility were measured. Subjects were categorized by diagnosis and imaging metrics were compared between groups using Student's t-tests. Receiver operating characteristic curves were generated for imaging metrics alone and in combination.
RESULTS: MRI scans for 43 patients with ALS or PLS and 15 patients with motor symptom predominant, non-upper motor neuron disease (mimics) were reviewed. Fractional anisotropy was lower (0.57 vs. 0.60, p < 0.01) and maximum motor cortex magnetic susceptibility higher (64.4 vs. 52.7, p = 0.01) in patients with ALS/PLS compared to mimics. There was no significant difference in area under the curve for these metrics alone (0.73, 0.63; p > 0.05) or in combination (0.75; p > 0.05).
CONCLUSION: We found significant differences in DTI and QSM metrics in patients with diseases affecting upper motor neurons (ALS/PLS) compared to mimics, but no significant difference in the performance of these metrics in diagnosing ALS/PLS compared to mimics.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; Diffusion tensor imaging; Motor neuron disease; Quantitative susceptibility mapping

Mesh:

Year:  2018        PMID: 30286313     DOI: 10.1016/j.clinimag.2018.09.015

Source DB:  PubMed          Journal:  Clin Imaging        ISSN: 0899-7071            Impact factor:   1.605


  3 in total

1.  Serial assessment of iron in the motor cortex in limb-onset amyotrophic lateral sclerosis using quantitative susceptibility mapping.

Authors:  Anjan Bhattarai; Zhaolin Chen; Phillip G D Ward; Paul Talman; Susan Mathers; Thanh G Phan; Caron Chapman; James Howe; Sarah Lee; Yennie Lie; Gary F Egan; Phyllis Chua
Journal:  Quant Imaging Med Surg       Date:  2020-07

Review 2.  Feature selection from magnetic resonance imaging data in ALS: a systematic review.

Authors:  Thomas D Kocar; Hans-Peter Müller; Albert C Ludolph; Jan Kassubek
Journal:  Ther Adv Chronic Dis       Date:  2021-10-13       Impact factor: 5.091

3.  Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases.

Authors:  Antonietta Canna; Francesca Trojsi; Federica Di Nardo; Giuseppina Caiazzo; Gioacchino Tedeschi; Mario Cirillo; Fabrizio Esposito
Journal:  Ann Clin Transl Neurol       Date:  2021-08-02       Impact factor: 4.511

  3 in total

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