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Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla
Published on: February 19, 2021
MR Imaging in Multiple Sclerosis: The Accuracy of 3D Double Inversion Recovery at 3 Tesla and the Potential for
1Department of Radiology, Royal Perth Hospital; Perth, Western Australia - simon.khangure@health.wa.gov.au.
Abstract:
To compare the accuracy of a three dimensional, T2-weighted double inversion recovery (DIR) sequence with two dimensional fluid attenuated inversion recovery (FLAIR) and dual echo T2 (DE T2) sequences at 3 Tesla in the detection of intracranial demyelinating lesions in patients with known or suspected multiple sclerosis (MS), and to consider the appropriateness of a stand-alone DIR sequence in MS imaging. The studies of 98 patients who underwent imaging with DE T2, FLAIR and DIR sequences for known or suspected multiple sclerosis were retrospectively reviewed. In 42 cases, a diagnosis of MS had been clinically suspected. In the remaining 56 cases, a diagnosis of MS had been previously established. All patients were imaged on a 3T MRI unit. Coronal and sagittal FLAIR, axial DE T2, and three dimensional T2-weighted DIR sequences were utilised. Of the 42 patients with suspected multiple sclerosis, 11 demonstrated lesions characteristic of the disease. Demyelinating plaques were seen in all of the 56 patients with known MS. In all cases, all lesions seen on DE T2-or FLAIR sequences were visible and more conspicuous on the DIR sequence. In 22 of the 67 patients (33%) with demyelinating lesions, the DIR sequence showed additional lesions not visible on any of the other sequences. Additional detected lesions predominantly involved grey matter. At 3 Tesla, a T2 weighted, three dimensional DIR sequence is as accurate at detecting the presence of intracranial demyelinating lesions as two dimensional FLAIR and DE T2 sequences combined. A greater number of lesions were detected with the DIR sequence, and all lesions were more conspicuous. A single, stand alone DIR sequence may be considered appropriate for monitoring MS.
Insights
A three-dimensional T2-weighted double inversion recovery (DIR) sequence is highly accurate for detecting multiple sclerosis (MS) brain lesions at 3 Tesla. This advanced MRI technique identifies more lesions, including those in grey matter, than traditional methods.
Area of Science:
- Radiology
- Neuroimaging
- Neurology
Background:
- Multiple sclerosis (MS) diagnosis and monitoring rely on detecting intracranial demyelinating lesions.
- Conventional MRI sequences like fluid attenuated inversion recovery (FLAIR) and dual echo T2 (DE T2) are used but may have limitations.
- Advanced imaging techniques are continuously explored to improve lesion detection and characterization.
Purpose of the Study:
- To compare the accuracy of a 3D T2-weighted double inversion recovery (DIR) sequence against 2D FLAIR and DE T2 sequences for detecting demyelinating lesions in patients with suspected or known MS.
- To evaluate the potential of a stand-alone DIR sequence for MS imaging at 3 Tesla.
Main Methods:
- Retrospective review of 98 patients with known or suspected MS who underwent 3 Tesla MRI.
- Imaging protocols included coronal/sagittal FLAIR, axial DE T2, and 3D T2-weighted DIR sequences.
- Comparison of lesion detection rates and conspicuity across the different sequences.
Main Results:
- The 3D DIR sequence detected all lesions visible on DE T2 and FLAIR sequences, with greater conspicuity.
- DIR identified additional demyelinating lesions in 33% of patients, predominantly in grey matter.
- At 3 Tesla, 3D DIR demonstrated comparable accuracy to combined DE T2 and FLAIR for detecting intracranial demyelinating lesions.
Conclusions:
- A 3D T2-weighted DIR sequence is a highly accurate tool for detecting intracranial demyelinating lesions in MS at 3 Tesla.
- The DIR sequence offers superior lesion detection and conspicuity, potentially identifying lesions missed by conventional sequences.
- A single, stand-alone DIR sequence may be suitable for monitoring MS, improving diagnostic and management efficiency.
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