A serial in vivo 7T magnetic resonance phase imaging study of white matter lesions in multiple sclerosis

Author:

Bian Wei12,Harter Kristin3,Hammond-Rosenbluth Kathryn E4,Lupo Janine M2,Xu Duan12,Kelley Douglas AC5,Vigneron Daniel B12,Nelson Sarah J126,Pelletier Daniel78

Affiliation:

1. The UC Berkeley & UCSF Graduate Program in Bioengineering, University of California San Francisco, USA

2. Department of Radiology and Biomedical Imaging, University of California San Francisco, USA

3. School of Pharmacy, University of California San Francisco, USA

4. Department of Neurological Surgery, University of California San Francisco, USA

5. GE Healthcare technologies, San Francisco, USA

6. Department of Bioengineeing and Therapeutic Sciences, University of California San Francisco, USA

7. Department of Neurology, University of California San Francisco, USA

8. Departments of Neurology and Diagnostic Radiology, Yale University, USA

Abstract

Background: Magnetic resonance (MR) phase imaging using high field MR scanners has demonstrated excellent contrast in multiple sclerosis (MS) lesions that is thought to be closely correlated to the local iron content. This pilot study acquired serial in vivo MR scans at 7T to track the evolution of phase contrast as MS lesions progress. Methods: Five MS patients with relapsing–remitting MS were serially scanned for about 2.5 years at 7T using a high resolution T2*-weighted gradient-echo sequence. Magnitude and phase images were reconstructed for each scan and co-registered to their baseline study. Results: Five non-enhancing ring and 70 nodular phase lesions were found in the five patients at baseline. None of the baseline phase lesions (including all five ring phase lesions) showed obvious qualitative variation on phase images during the study. Of note, we observed that three magnitude lesions, not initially read as abnormal signal, were either better appreciated using phase contrast imaging (two lesions) or preceded (one lesion) by phase changes. Conclusion: The observation that ring phase lesions remained unchanged over 2.5 years of follow-up challenges the notion that such lesions reveal the presence of acute activated iron-rich macrophages. It suggests that either different phenotypes of macrophages persist longer than previously expected or other mechanisms related to tissue injury contribute to the phase contrast.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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